Gastrointestinal Tract - Liver Development

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Introduction

Embryonic hepatic bud formation.

This section of notes gives an overview of how the liver develops. The transverse septum (septum transversum) arises at an embryonic junctional site. The junctional region externally is where the ectoderm of the amnion meets the endoderm of the yolk sac. The junctional region internally is where the foregut meets the midgut. The mesenchymal structure of the transverse septum provides a support within which both blood vessels and the liver begin to form. Arises at embryonic junction (septum transversum): externally is where ectoderm of amnion meets endoderm of yolk sac and internally is where the foregut meets the midgut. Mesenchymal structure of transverse septum provides a support within which both blood vessels and liver begin to form in the underlying splanchnic mesoderm.


In the early embryo, the liver and heart grow rapidly forming obvious external swellings on the ventral embryo surface. The liver's initial embryonic function is mainly cardiovascular. Firstly, as a vascular connection between the developing placental vessels to the heart. Secondly, as a haemopoietic tissue where blood stem cells reside before bone marrow development.


See also Liver Histology showing both developmental and adult histology.


GIT Links: Introduction | Medicine Lecture | Science Lecture | Endoderm | Stomach | Liver | Gall Bladder | Pancreas | Intestine | Tongue | Taste | Enteric Nervous System | Stage 13 | Stage 22 | Abnormalities | Movies | Postnatal | Milk | Tooth | Tongue | BGD Lecture | BGD Practical | Category:Gastrointestinal Tract
GIT Histology Links: Upper GIT | Salivary Gland | Smooth Muscle Histology | Liver | Gall Bladder | Pancreas | Colon | Histology Stains | Histology | GIT Development
Historic Embryology
1878 Alimentary Canal | 1882 The Organs of the Inner Germ-Layer The Alimentary Tube with its Appended Organs | 1902 The Organs of Digestion | 1906 Liver | 1907 Development of the Digestive System | 1907 Atlas | 1907 23 Somite Embryo | 1912 Digestive Tract | 1917 Entodermal Canal | 1918 Anatomy | 1921 Alimentary Tube | 2014 GIT Notes | Historic Disclaimer
Human Embryo: 1908 13-14 Somite Embryo | 1926 22 Somite Embryo | 1907 23 Somite Embryo | 1937 25 Somite Embryo | 1914 27 Somite Embryo | 1914 Week 7 Embryo
Animal Development: 1913 Chicken | 1951 Frog
Historic Embryology:1912 Liver

Some Recent Findings

Human Liver (week 8, GA week 10)
  • Three-dimensional reconstructions of intrahepatic bile duct tubulogenesis in human liver[1] "Samples from human prenatal livers ranging from 7 weeks + 2 days to 15½ weeks post conception as well as adult normal and acetaminophen intoxicated liver were used. ....In the developing human liver, three-dimensional reconstructions using multiple marker proteins confirmed that the human intrahepatic biliary tree forms through several developmental stages involving an initial transition of primitive hepatocytes into cholangiocytes shaping the ductal plate followed by a process of maturation and remodeling where the intrahepatic biliary tree develops through an asymmetrical form of cholangiocyte tubulogenesis.
  • Dynamic signaling network for the specification of embryonic pancreas and liver progenitors [2] Studies of the formation of pancreas and liver progenitors have focused on individual inductive signals and cellular responses. Here, we investigated how bone morphogenetic protein, transforming growth factor-beta (TGFbeta), and fibroblast growth factor signaling pathways converge on the earliest genes that elicit pancreas and liver induction in mouse embryos. The inductive network was found to be dynamic; it changed within hours. Different signals functioned in parallel to induce different early genes, and two permutations of signals induced liver progenitor domains, which revealed flexibility in cell programming. Also, the specification of pancreas and liver progenitors was restricted by the TGFbeta pathway."
  • Notch signaling controls liver development by regulating biliary differentiation[3]In the mammalian liver, bile is transported to the intestine through an intricate network of bile ducts. Notch signaling is required for normal duct formation, but its mode of action has been unclear. Here, we show in mice that bile ducts arise through a novel mechanism of tubulogenesis involving sequential radial differentiation. Notch signaling is activated in a subset of liver progenitor cells fated to become ductal cells, and pathway activation is necessary for biliary fate."
More recent papers
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  • Therefore the list of references do not reflect any editorial selection of material based on content or relevance.
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References listed on the rest of the content page and the associated discussion page (listed under the publication year sub-headings) do include some editorial selection based upon both relevance and availability.

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Search term: Liver Embryology

Ahmet Bal, Yucel Gonul, Omer Hazman, Ahmet Kocak, Mehmet Fatih Bozkurt, Sezgin Yilmaz, Serdar Kokulu, Oya Oruc, Kasim Demir Interleukin 18-binding protein ameliorates liver ischemia-reperfusion injury. J. Surg. Res.: 2016, 201(1);13-21 PubMed 26850179

F Yigit, E Gurel-Gurevin, B Isbilen-Basok, Obb Esener, T Bilal, O Keser, A Altiner, N Yilmazer, E I Ikitimur-Armutak Protective effect of Spirulina platensis against cell damage and apoptosis in hepatic tissue caused by high fat diet. Biotech Histochem: 2016;1-13 PubMed 26820259

Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, Md Joynal Abedin, Hagai Abeliovich, Abraham Acevedo Arozena, Hiroaki Adachi, Christopher M Adams, Peter D Adams, Khosrow Adeli, Peter J Adhihetty, Sharon G Adler, Galila Agam, Rajesh Agarwal, Manish K Aghi, Maria Agnello, Patrizia Agostinis, Patricia V Aguilar, Julio Aguirre-Ghiso, Edoardo M Airoldi, Slimane Ait-Si-Ali, Takahiko Akematsu, Emmanuel T Akporiaye, Mohamed Al-Rubeai, Guillermo M Albaiceta, Chris Albanese, Diego Albani, Matthew L Albert, Jesus Aldudo, Hana Algül, Mehrdad Alirezaei, Iraide Alloza, Alexandru Almasan, Maylin Almonte-Beceril, Emad S Alnemri, Covadonga Alonso, Nihal Altan-Bonnet, Dario C Altieri, Silvia Alvarez, Lydia Alvarez-Erviti, Sandro Alves, Giuseppina Amadoro, Atsuo Amano, Consuelo Amantini, Santiago Ambrosio, Ivano Amelio, Amal O Amer, Mohamed Amessou, Angelika Amon, Zhenyi An, Frank A Anania, Stig U Andersen, Usha P Andley, Catherine K Andreadi, Nathalie Andrieu-Abadie, Alberto Anel, David K Ann, Shailendra Anoopkumar-Dukie, Manuela Antonioli, Hiroshi Aoki, Nadezda Apostolova, Saveria Aquila, Katia Aquilano, Koichi Araki, Eli Arama, Agustin Aranda, Jun Araya, Alexandre Arcaro, Esperanza Arias, Hirokazu Arimoto, Aileen R Ariosa, Jane L Armstrong, Thierry Arnould, Ivica Arsov, Katsuhiko Asanuma, Valerie Askanas, Eric Asselin, Ryuichiro Atarashi, Sally S Atherton, Julie D Atkin, Laura D Attardi, Patrick Auberger, Georg Auburger, Laure Aurelian, Riccardo Autelli, Laura Avagliano, Maria Laura Avantaggiati, Limor Avrahami, Suresh Awale, Neelam Azad, Tiziana Bachetti, Jonathan M Backer, Dong-Hun Bae, Jae-Sung Bae, Ok-Nam Bae, Soo Han Bae, Eric H Baehrecke, Seung-Hoon Baek, Stephen Baghdiguian, Agnieszka Bagniewska-Zadworna, Hua Bai, Jie Bai, Xue-Yuan Bai, Yannick Bailly, Kithiganahalli Narayanaswamy Balaji, Walter Balduini, Andrea Ballabio, Rena Balzan, Rajkumar Banerjee, Gábor Bánhegyi, Haijun Bao, Benoit Barbeau, Maria D Barrachina, Esther Barreiro, Bonnie Bartel, Alberto Bartolomé, Diane C Bassham, Maria Teresa Bassi, Robert C Bast, Alakananda Basu, Maria Teresa Batista, Henri Batoko, Maurizio Battino, Kyle Bauckman, Bradley L Baumgarner, K Ulrich Bayer, Rupert Beale, Jean-François Beaulieu, George R Beck, Christoph Becker, J David Beckham, Pierre-André Bédard, Patrick J Bednarski, Thomas J Begley, Christian Behl, Christian Behrends, Georg Mn Behrens, Kevin E Behrns, Eloy Bejarano, Amine Belaid, Francesca Belleudi, Giovanni Bénard, Guy Berchem, Daniele Bergamaschi, Matteo Bergami, Ben Berkhout, Laura Berliocchi, Amélie Bernard, Monique Bernard, Francesca Bernassola, Anne Bertolotti, Amanda S Bess, Sébastien Besteiro, Saverio Bettuzzi, Savita Bhalla, Shalmoli Bhattacharyya, Sujit K Bhutia, Caroline Biagosch, Michele Wolfe Bianchi, Martine Biard-Piechaczyk, Viktor Billes, Claudia Bincoletto, Baris Bingol, Sara W Bird, Marc Bitoun, Ivana Bjedov, Craig Blackstone, Lionel Blanc, Guillermo A Blanco, Heidi Kiil Blomhoff, Emilio Boada-Romero, Stefan Böckler, Marianne Boes, Kathleen Boesze-Battaglia, Lawrence H Boise, Alessandra Bolino, Andrea Boman, Paolo Bonaldo, Matteo Bordi, Jürgen Bosch, Luis M Botana, Joelle Botti, German Bou, Marina Bouché, Marion Bouchecareilh, Marie-Josée Boucher, Michael E Boulton, Sebastien G Bouret, Patricia Boya, Michaël Boyer-Guittaut, Peter V Bozhkov, Nathan Brady, Vania Mm Braga, Claudio Brancolini, Gerhard H Braus, José M Bravo-San Pedro, Lisa A Brennan, Emery H Bresnick, Patrick Brest, Dave Bridges, Marie-Agnès Bringer, Marisa Brini, Glauber C Brito, Bertha Brodin, Paul S Brookes, Eric J Brown, Karen Brown, Hal E Broxmeyer, Alain Bruhat, Patricia Chakur Brum, John H Brumell, Nicola Brunetti-Pierri, Robert J Bryson-Richardson, Shilpa Buch, Alastair M Buchan, Hikmet Budak, Dmitry V Bulavin, Scott J Bultman, Geert Bultynck, Vladimir Bumbasirevic, Yan Burelle, Robert E Burke, Margit Burmeister, Peter Bütikofer, Laura Caberlotto, Ken Cadwell, Monika Cahova, Dongsheng Cai, Jingjing Cai, Qian Cai, Sara Calatayud, Nadine Camougrand, Michelangelo Campanella, Grant R Campbell, Matthew Campbell, Silvia Campello, Robin Candau, Isabella Caniggia, Lavinia Cantoni, Lizhi Cao, Allan B Caplan, Michele Caraglia, Claudio Cardinali, Sandra Morais Cardoso, Jennifer S Carew, Laura A Carleton, Cathleen R Carlin, Silvia Carloni, Sven R Carlsson, Didac Carmona-Gutierrez, Leticia Am Carneiro, Oliana Carnevali, Serena Carra, Alice Carrier, Bernadette Carroll, Caty Casas, Josefina Casas, Giuliana Cassinelli, Perrine Castets, Susana Castro-Obregon, Gabriella Cavallini, Isabella Ceccherini, Francesco Cecconi, Arthur I Cederbaum, Valentín Ceña, Simone Cenci, Claudia Cerella, Davide Cervia, Silvia Cetrullo, Hassan Chaachouay, Han-Jung Chae, Andrei S Chagin, Chee-Yin Chai, Gopal Chakrabarti, Georgios Chamilos, Edmond Yw Chan, Matthew Tv Chan, Dhyan Chandra, Pallavi Chandra, Chih-Peng Chang, Raymond Chuen-Chung Chang, Ta Yuan Chang, John C Chatham, Saurabh Chatterjee, Santosh Chauhan, Yongsheng Che, Michael E Cheetham, Rajkumar 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Chuang, Taehoon Chun, Hyewon Chung, Taijoon Chung, Yuen-Li Chung, Yong-Joon Chwae, Valentina Cianfanelli, Roberto Ciarcia, Iwona A Ciechomska, Maria Rosa Ciriolo, Mara Cirone, Sofie Claerhout, Michael J Clague, Joan Clària, Peter Gh Clarke, Robert Clarke, Emilio Clementi, Cédric Cleyrat, Miriam Cnop, Eliana M Coccia, Tiziana Cocco, Patrice Codogno, Jörn Coers, Ezra Ew Cohen, David Colecchia, Luisa Coletto, Núria S Coll, Emma Colucci-Guyon, Sergio Comincini, Maria Condello, Katherine L Cook, Graham H Coombs, Cynthia D Cooper, J Mark Cooper, Isabelle Coppens, Maria Tiziana Corasaniti, Marco Corazzari, Ramon Corbalan, Elisabeth Corcelle-Termeau, Mario D Cordero, Cristina Corral-Ramos, Olga Corti, Andrea Cossarizza, Paola Costelli, Safia Costes, Susan L Cotman, Ana Coto-Montes, Sandra Cottet, Eduardo Couve, Lori R Covey, L Ashley Cowart, Jeffery S Cox, Fraser P Coxon, Carolyn B Coyne, Mark S Cragg, Rolf J Craven, Tiziana Crepaldi, Jose L Crespo, Alfredo Criollo, Valeria Crippa, Maria Teresa Cruz, Ana Maria Cuervo, Jose M Cuezva, Taixing Cui, Pedro R Cutillas, Mark J Czaja, Maria F Czyzyk-Krzeska, Ruben K Dagda, Uta Dahmen, Chunsun Dai, Wenjie Dai, Yun Dai, Kevin N Dalby, Luisa Dalla Valle, Guillaume Dalmasso, Marcello D'Amelio, Markus Damme, Arlette Darfeuille-Michaud, Catherine Dargemont, Victor M Darley-Usmar, Srinivasan Dasarathy, Biplab Dasgupta, Srikanta Dash, Crispin R Dass, Hazel Marie Davey, Lester M Davids, David Dávila, Roger J Davis, Ted M Dawson, Valina L Dawson, Paula Daza, Jackie de Belleroche, Paul de Figueiredo, Regina Celia Bressan Queiroz de Figueiredo, José de la Fuente, Luisa De Martino, Antonella De Matteis, Guido Ry De Meyer, Angelo De Milito, Mauro De Santi, Wanderley de Souza, Vincenzo De Tata, Daniela De Zio, Jayanta Debnath, Reinhard Dechant, Jean-Paul Decuypere, Shane Deegan, Benjamin Dehay, Barbara Del Bello, Dominic P Del Re, Régis Delage-Mourroux, Lea Md Delbridge, Louise Deldicque, Elizabeth Delorme-Axford, Yizhen Deng, Joern Dengjel, 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Verónica I Dumit, Mara C Duncan, Elaine A Dunlop, William A Dunn, Nicolas Dupont, Luc Dupuis, Raúl V Durán, Thomas M Durcan, Stéphane Duvezin-Caubet, Umamaheswar Duvvuri, Vinay Eapen, Darius Ebrahimi-Fakhari, Arnaud Echard, Leopold Eckhart, Charles L Edelstein, Aimee L Edinger, Ludwig Eichinger, Tobias Eisenberg, Avital Eisenberg-Lerner, N Tony Eissa, Wafik S El-Deiry, Victoria El-Khoury, Zvulun Elazar, Hagit Eldar-Finkelman, Chris Jh Elliott, Enzo Emanuele, Urban Emmenegger, Nikolai Engedal, Anna-Mart Engelbrecht, Simone Engelender, Jorrit M Enserink, Ralf Erdmann, Jekaterina Erenpreisa, Rajaraman Eri, Jason L Eriksen, Andreja Erman, Ricardo Escalante, Eeva-Liisa Eskelinen, Lucile Espert, Lorena Esteban-Martínez, Thomas J Evans, Mario Fabri, Gemma Fabrias, Cinzia Fabrizi, Antonio Facchiano, Nils J Færgeman, Alberto Faggioni, W Douglas Fairlie, Chunhai Fan, Daping Fan, Jie Fan, Shengyun Fang, Manolis Fanto, Alessandro Fanzani, Thomas Farkas, Mathias Faure, Francois B Favier, Howard Fearnhead, Massimo Federici, Erkang Fei, Tania C Felizardo, Hua Feng, Yibin Feng, Yuchen Feng, Thomas A Ferguson, Álvaro F Fernández, Maite G Fernandez-Barrena, Jose C Fernandez-Checa, Arsenio Fernández-López, Martin E Fernandez-Zapico, Olivier Feron, Elisabetta Ferraro, Carmen Veríssima Ferreira-Halder, Laszlo Fesus, Ralph Feuer, Fabienne C Fiesel, Eduardo C Filippi-Chiela, Giuseppe Filomeni, Gian Maria Fimia, John H Fingert, Steven Finkbeiner, Toren Finkel, Filomena Fiorito, Paul B Fisher, Marc Flajolet, Flavio Flamigni, Oliver Florey, Salvatore Florio, R Andres Floto, Marco Folini, Carlo Follo, Edward A Fon, Francesco Fornai, Franco Fortunato, Alessandro Fraldi, Rodrigo Franco, Arnaud Francois, Aurélie François, Lisa B Frankel, Iain Dc Fraser, Norbert Frey, Damien G Freyssenet, Christian Frezza, Scott L Friedman, Daniel E Frigo, Dongxu Fu, José M Fuentes, Juan Fueyo, Yoshio Fujitani, Yuuki Fujiwara, Mikihiro Fujiya, Mitsunori Fukuda, Simone Fulda, Carmela Fusco, Bozena Gabryel, Matthias Gaestel, Philippe Gailly, Malgorzata Gajewska, Sehamuddin Galadari, Gad Galili, Inmaculada Galindo, Maria F Galindo, Giovanna Galliciotti, Lorenzo Galluzzi, Luca Galluzzi, Vincent Galy, Noor Gammoh, Sam Gandy, Anand K Ganesan, Swamynathan Ganesan, Ian G Ganley, Monique Gannagé, Fen-Biao Gao, Feng Gao, Jian-Xin Gao, Lorena García Nannig, Eleonora García Véscovi, Marina Garcia-Macía, Carmen Garcia-Ruiz, Abhishek D Garg, Pramod Kumar Garg, Ricardo Gargini, Nils Christian Gassen, Damián Gatica, Evelina Gatti, Julie Gavard, Evripidis Gavathiotis, Liang Ge, Pengfei Ge, Shengfang Ge, Po-Wu Gean, Vania Gelmetti, Armando A Genazzani, Jiefei Geng, Pascal Genschik, Lisa Gerner, Jason E Gestwicki, David A Gewirtz, Saeid Ghavami, Eric Ghigo, Debabrata Ghosh, Anna Maria Giammarioli, Francesca Giampieri, Claudia Giampietri, Alexandra Giatromanolaki, Derrick J Gibbings, Lara Gibellini, Spencer B Gibson, Vanessa Ginet, Antonio Giordano, Flaviano Giorgini, Elisa Giovannetti, Stephen E Girardin, Suzana Gispert, Sandy Giuliano, Candece L Gladson, Alvaro Glavic, Martin Gleave, Nelly Godefroy, Robert M Gogal, Kuppan Gokulan, Gustavo H Goldman, Delia Goletti, Michael S Goligorsky, Aldrin V Gomes, Ligia C Gomes, Hernando Gomez, Candelaria Gomez-Manzano, Rubén Gómez-Sánchez, Dawit Ap Gonçalves, Ebru Goncu, Qingqiu Gong, Céline Gongora, Carlos B Gonzalez, Pedro Gonzalez-Alegre, Pilar Gonzalez-Cabo, Rosa Ana González-Polo, Ing Swie Goping, Carlos Gorbea, Nikolai V Gorbunov, Daphne R Goring, Adrienne M Gorman, Sharon M Gorski, Sandro Goruppi, Shino Goto-Yamada, Cecilia Gotor, Roberta A Gottlieb, Illana Gozes, Devrim Gozuacik, Yacine Graba, Martin Graef, Giovanna E Granato, Gary Dean Grant, Steven Grant, Giovanni Luca Gravina, Douglas R Green, Alexander Greenhough, Michael T Greenwood, Benedetto Grimaldi, Frédéric Gros, Charles Grose, Jean-Francois Groulx, Florian Gruber, Paolo Grumati, Tilman Grune, Jun-Lin Guan, Kun-Liang Guan, Barbara Guerra, Carlos Guillen, Kailash Gulshan, Jan Gunst, Chuanyong Guo, Lei Guo, Ming Guo, Wenjie Guo, Xu-Guang Guo, Andrea A Gust, Åsa B Gustafsson, Elaine Gutierrez, Maximiliano G Gutierrez, Ho-Shin Gwak, Albert Haas, James E Haber, Shinji Hadano, Monica Hagedorn, David R Hahn, Andrew J Halayko, Anne Hamacher-Brady, Kozo Hamada, Ahmed Hamai, Andrea Hamann, Maho Hamasaki, Isabelle Hamer, Qutayba Hamid, Ester M Hammond, Feng Han, Weidong Han, James T Handa, John A Hanover, Malene Hansen, Masaru Harada, Ljubica Harhaji-Trajkovic, J Wade Harper, Abdel Halim Harrath, Adrian L Harris, James Harris, Udo Hasler, Peter Hasselblatt, Kazuhisa Hasui, Robert G Hawley, Teresa S Hawley, Congcong He, Cynthia Y He, Fengtian He, Gu He, Rong-Rong He, Xian-Hui He, You-Wen He, Yu-Ying He, Joan K Heath, Marie-Josée Hébert, Robert A Heinzen, Gudmundur Vignir Helgason, Michael Hensel, Elizabeth P Henske, Chengtao Her, Paul K Herman, Agustín Hernández, Carlos Hernandez, Sonia Hernández-Tiedra, Claudio Hetz, P Robin Hiesinger, Katsumi Higaki, Sabine Hilfiker, Bradford G Hill, Joseph A Hill, William D Hill, Keisuke Hino, Daniel Hofius, Paul Hofman, Günter U Höglinger, Jörg Höhfeld, Marina K Holz, Yonggeun Hong, David A Hood, Jeroen Jm Hoozemans, Thorsten Hoppe, Chin Hsu, Chin-Yuan Hsu, Li-Chung Hsu, Dong Hu, Guochang Hu, Hong-Ming Hu, Hongbo Hu, Ming Chang Hu, Yu-Chen Hu, Zhuo-Wei Hu, Fang Hua, Ya Hua, Canhua Huang, Huey-Lan Huang, Kuo-How Huang, Kuo-Yang Huang, Shile Huang, Shiqian Huang, Wei-Pang Huang, Yi-Ran Huang, Yong Huang, Yunfei Huang, Tobias B Huber, Patricia Huebbe, Won-Ki Huh, Juha J Hulmi, Gang Min Hur, James H Hurley, Zvenyslava Husak, Sabah Na Hussain, Salik Hussain, Jung Jin Hwang, Seungmin Hwang, Thomas Is Hwang, Atsuhiro Ichihara, Yuzuru Imai, Carol Imbriano, Megumi Inomata, Takeshi Into, Valentina Iovane, Juan L Iovanna, Renato V Iozzo, Nancy Y Ip, Javier E Irazoqui, Pablo Iribarren, Yoshitaka Isaka, Aleksandra J Isakovic, Harry Ischiropoulos, Jeffrey S Isenberg, Mohammad Ishaq, Hiroyuki Ishida, Isao Ishii, Jane E Ishmael, Ciro Isidoro, Ken-Ichi Isobe, Erika Isono, Shohreh Issazadeh-Navikas, Koji Itahana, Eisuke Itakura, Andrei I Ivanov, Anand Krishnan V Iyer, José M Izquierdo, Yotaro Izumi, Valentina Izzo, Marja Jäättelä, Nadia Jaber, Daniel John Jackson, William T Jackson, Tony George Jacob, Thomas S Jacques, Chinnaswamy Jagannath, Ashish Jain, Nihar Ranjan Jana, Byoung Kuk Jang, Alkesh Jani, Bassam Janji, Paulo Roberto Jannig, Patric J Jansson, Steve Jean, Marina Jendrach, Ju-Hong Jeon, Niels Jessen, Eui-Bae Jeung, Kailiang Jia, Lijun Jia, Hong Jiang, Hongchi Jiang, Liwen Jiang, Teng Jiang, Xiaoyan Jiang, Xuejun Jiang, Xuejun Jiang, Ying Jiang, Yongjun Jiang, Alberto Jiménez, Cheng Jin, Hongchuan Jin, Lei Jin, Meiyan Jin, Shengkan Jin, Umesh Kumar Jinwal, Eun-Kyeong Jo, Terje Johansen, Daniel E Johnson, Gail Vw Johnson, James D Johnson, Eric Jonasch, Chris Jones, Leo Ab Joosten, Joaquin Jordan, Anna-Maria Joseph, Bertrand Joseph, Annie M Joubert, Dianwen Ju, Jingfang Ju, Hsueh-Fen Juan, 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Arianna L Kim, Cheol Hyeon Kim, Deok Ryong Kim, Do-Hyung Kim, Eung Kweon Kim, Hye Young Kim, Hyung-Ryong Kim, Jae-Sung Kim, Jeong Hun Kim, Jin Cheon Kim, Jin Hyoung Kim, Kwang Woon Kim, Michael D Kim, Moon-Moo Kim, Peter K Kim, Seong Who Kim, Soo-Youl Kim, Yong-Sun Kim, Yonghyun Kim, Adi Kimchi, Alec C Kimmelman, Tomonori Kimura, Jason S King, Karla Kirkegaard, Vladimir Kirkin, Lorrie A Kirshenbaum, Shuji Kishi, Yasuo Kitajima, Katsuhiko Kitamoto, Yasushi Kitaoka, Kaio Kitazato, Rudolf A Kley, Walter T Klimecki, Michael Klinkenberg, Jochen Klucken, Helene Knævelsrud, Erwin Knecht, Laura Knuppertz, Jiunn-Liang Ko, Satoru Kobayashi, Jan C Koch, Christelle Koechlin-Ramonatxo, Ulrich Koenig, Young Ho Koh, Katja Köhler, Sepp D Kohlwein, Masato Koike, Masaaki Komatsu, Eiki Kominami, Dexin Kong, Hee Jeong Kong, Eumorphia G Konstantakou, Benjamin T Kopp, Tamas Korcsmaros, Laura Korhonen, Viktor I Korolchuk, Nadya V Koshkina, Yanjun Kou, Michael I Koukourakis, Constantinos Koumenis, Attila L 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Chris Williams, Katherine Williams, Peter R Williamson, Konstanze F Winklhofer, Steven S Witkin, Stephanie E Wohlgemuth, Thomas Wollert, Ernst J Wolvetang, Esther Wong, G William Wong, Richard W Wong, Vincent Kam Wai Wong, Elizabeth A Woodcock, Karen L Wright, Chunlai Wu, Defeng Wu, Gen Sheng Wu, Jian Wu, Junfang Wu, Mian Wu, Min Wu, Shengzhou Wu, William Kk Wu, Yaohua Wu, Zhenlong Wu, Cristina Pr Xavier, Ramnik J Xavier, Gui-Xian Xia, Tian Xia, Weiliang Xia, Yong Xia, Hengyi Xiao, Jian Xiao, Shi Xiao, Wuhan Xiao, Chuan-Ming Xie, Zhiping Xie, Zhonglin Xie, Maria Xilouri, Yuyan Xiong, Chuanshan Xu, Congfeng Xu, Feng Xu, Haoxing Xu, Hongwei Xu, Jian Xu, Jianzhen Xu, Jinxian Xu, Liang Xu, Xiaolei Xu, Yangqing Xu, Ye Xu, Zhi-Xiang Xu, Ziheng Xu, Yu Xue, Takahiro Yamada, Ai Yamamoto, Koji Yamanaka, Shunhei Yamashina, Shigeko Yamashiro, Bing Yan, Bo Yan, Xianghua Yan, Zhen Yan, Yasuo Yanagi, Dun-Sheng Yang, Jin-Ming Yang, Liu Yang, Minghua Yang, Pei-Ming Yang, Peixin Yang, Qian Yang, Wannian Yang, Wei Yuan Yang, Xuesong Yang, Yi Yang, Ying Yang, Zhifen Yang, Zhihong Yang, Meng-Chao Yao, Pamela J Yao, Xiaofeng Yao, Zhenyu Yao, Zhiyuan Yao, Linda S Yasui, Mingxiang Ye, Barry Yedvobnick, Behzad Yeganeh, Elizabeth S Yeh, Patricia L Yeyati, Fan Yi, Long Yi, Xiao-Ming Yin, Calvin K Yip, Yeong-Min Yoo, Young Hyun Yoo, Seung-Yong Yoon, Ken-Ichi Yoshida, Tamotsu Yoshimori, Ken H Young, Huixin Yu, Jane J Yu, Jin-Tai Yu, Jun Yu, Li Yu, W Haung Yu, Xiao-Fang Yu, Zhengping Yu, Junying Yuan, Zhi-Min Yuan, Beatrice Yjt Yue, Jianbo Yue, Zhenyu Yue, David N Zacks, Eldad Zacksenhaus, Nadia Zaffaroni, Tania Zaglia, Zahra Zakeri, Vincent Zecchini, Jinsheng Zeng, Min Zeng, Qi Zeng, Antonis S Zervos, Donna D Zhang, Fan Zhang, Guo Zhang, Guo-Chang Zhang, Hao Zhang, Hong Zhang, Hong Zhang, Hongbing Zhang, Jian Zhang, Jian Zhang, Jiangwei Zhang, Jianhua Zhang, Jing-Pu Zhang, Li Zhang, Lin Zhang, Lin Zhang, Long Zhang, Ming-Yong Zhang, Xiangnan Zhang, Xu Dong Zhang, Yan Zhang, Yang Zhang, Yanjin Zhang, Yingmei Zhang, Yunjiao Zhang, Mei Zhao, Wei-Li Zhao, Xiaonan Zhao, Yan G Zhao, Ying Zhao, Yongchao Zhao, Yu-Xia Zhao, Zhendong Zhao, Zhizhuang J Zhao, Dexian Zheng, Xi-Long Zheng, Xiaoxiang Zheng, Boris Zhivotovsky, Qing Zhong, Guang-Zhou Zhou, Guofei Zhou, Huiping Zhou, Shu-Feng Zhou, Xu-Jie Zhou, Hongxin Zhu, Hua Zhu, Wei-Guo Zhu, Wenhua Zhu, Xiao-Feng Zhu, Yuhua Zhu, Shi-Mei Zhuang, Xiaohong Zhuang, Elio Ziparo, Christos E Zois, Teresa Zoladek, Wei-Xing Zong, Antonio Zorzano, Susu M Zughaier Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). 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Tine M Comhair, Sonia C Garcia Caraballo, Cornelis H C Dejong, Wouter H Lamers, S Eleonore Koehler The odd-carbon medium-chain fatty triglyceride triheptanoin does not reduce hepatic steatosis. Clin Nutr: 2015; PubMed 26778339

Mehmet Zulkuf Akdag, Suleyman Dasdag, Fazile Canturk, Derya Karabulut, Yusuf Caner, Nur Adalier Does prolonged radiofrequency radiation emitted from Wi-Fi devices induce DNA damage in various tissues of rats? J. Chem. Neuroanat.: 2016; PubMed 26775760

Movies

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 ‎‎Lesser sac
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 ‎‎Greater Omentum
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Liver Development Stages

Human Liver Growth (weight grams)[4]
Carnegie Stage
Feature
11
hepatic diverticulum development
12
cell differentiation

septum transversum forming liver stroma

hepatic diverticulum forming hepatic trabeculae

13
epithelial cord proliferation enmeshing stromal capillaries
14
hepatic gland and its vascular channels enlarge

hematopoietic function appeared

18
obturation due to epithelial proliferation

bile ducts became reorganized (continuity between liver cells and gut)

18 to 23
biliary ductules developed in periportal connective tissue

produces ductal plates that receive biliary capillaries

Human data from Godlewski G, etal,[5] see also liver development in the rat during the embryonic period (Carnegie stages 15-23).[6] (More? Timeline human development)
Embryonic Liver Development Timeline
This information is from a recent study[7] of the human embryonic liver from week 5 to 8 (GA 7 to 9; Carnegie stage 14 to 23).
Carnegie Stage Age CRL (mm) Biliary system Vascular Hepatic parenchyma
14 33 7
  • Primordial bile duct (links primitive intestine and liver parenchyma) visible. Thick-walled tube (95􏰁 µm diameter) with a small lumen (22 µ􏰁m in diameter).
  • Gallbladder - elongated tube further dilated, thick wall (125􏰁 µm in diameter) and a narrow lumen (43􏰁 µm of diameter).
  • Intra-hepatic vasculature is represented by the presence of hepatic sinusoids.
  • Three venous tributaries flow into the liver sinusoids: a large right umbilical vein, a large left placental vein and a single vitelline vein.
  • Cords of liver cells are fragmented by vascular network of the hepatic sinusoids.
  • Located between the pericardial cavity at the top and the mesonephros at the bottom.
  • Upper pole of the liver lies close to the septum transversum and early ventricles.
  • Liver occupies the majority of abdominal cavity.
18 46 15
  • Bile duct (future common bile duct), and a common hepatic duct, which is in contact with the liver parenchyma without penetration.
  • Primordium of accessory bile tract is an elongated and fusiform gall bladder projecting forward and by a short cystic duct that opens into the common bile duct.
  • The bile duct empties into the second part of duodenum on its posterior side.
  • Portal system visible - portal vein (100 µ􏰁m diameter) arises from the connection of the upper mesenteric vein then at region of the hepatic hilum (285􏰁 µm) divides into portal branches.
  • Left umbilical vein empties into the anterior extremity of the left portal branch.
  • Ductus venosus (80 µm) connects the initial portion of left portal vein to the inferior vena cava.
  • Hepatic venous system 3 branches - left hepatic vein (120􏰁 µm in diameter), middle hepatic vein (220 􏰁µm in diameter) and right hepatic vein (160􏰁 µm in diameter). Flows into the sub-cardinal vein.
  • Liver parenchyma has two anatomical lobes, a right lobe and a left lobe, separated by the anteroposterior plane formed by the placental vein.
21 53 22.5 Bile duct morphology as earlier stage. Common bile duct empties at the level of the proximal duodenum.
  • Portal vein arises from the joining of the splenic vein and the superior mesenteric vein. At the level of the hepatic hilum, portal vein divides into two branches, right portal branch (420 µm in diameter) and left portal branch (540 􏰁m in diameter). Right portal branch gives rise to a thin branch to the caudate lobe. Ventral branch gives rise to segmental portal veins (VIII and V). Dorsal branch gives rise to the segmental portal veins (VI and VII).
  • Ductus venosus connects the initial portion of the left portal vein to the inferior vena cava just upstream from the hepatic vein afferents.
  • Hepatic venous system as for previous stage.
Hepatic parenchyma looks like a large rounded mass.
23 58 27 Bile duct morphology as earlier stage.
  • Portal venous system complete.
  • Ductus venosus (40 m) connects the initial portion of the portal vein to the middle hepatic vein.
  • hepatic venous system has changed very little from the previous stage. the three hepatic veins empty into the inferior vena cava.
  • Liver parenchyma has a roughly oval shape. Two symmetrical hepatic lobes are identifiable. The quadrate and caudate lobes are identifiable.
  • Upper pole of the liver is always bounded above by the diaphragm.
Links: Liver Development | Carnegie stage 14 | Carnegie stage 18 | Carnegie stage 21 | Carnegie stage 23 | Timeline human development

Liver Buds

  • Differentiates to form the hepatic diverticulum and hepatic primordium, generates the gall bladder then divides into right and left hepatic (liver) buds.
  • Three connecting stalks (cystic duct, hepatic ducts) which fuse to form bile duct.

Left Hepatic Bud

  • left lobe, quadrate, caudate (both q and c anatomically Left)
  • caudate lobe of human liver consists of 3 anatomical parts: Spiegel's lobe, caudate process, and paracaval portion.

Right Hepatic Bud

  • right lobe

Liver Structural Origins

The Liver Lobule
  • Hepatic Buds - form hepatocytes, produce bile from week 13 (forms meconium of newborn)
  • Vitelline Veins - form sinusoids
  • Mesenchyme - form connective tissue and Kupffer cells

Function - Haemopoiesis

Embryonic liver also involved in blood formation, after the yolk sac and blood islands acting as a primary site.

Components of Liver Formation

Mouse liver development signaling.[8]

Primitive Endoderm

  • foregut diverticulum
  • foregut-midgut junction
    • septum transversum
      • hepatic diverticulum
        • cystic primordium
          • gall bladder
            • common bile duct
              • hepatic ducts
                • liver/gall bladder
      • hepatic primordium
        • hepatic parenchyma
          • hepatic sinusoids
            • lobes of liver
              • liver/gall bladder
  • midgut region
  • hindgut diverticulum (pocket)

Data from mouse [9]


Hepatoblasts - endoderm-derived cells can differentiate into either:

  1. hepatocytes - populate the bulk of the liver parenchyma.
  2. cholangiocytes - line the intrahepatic bile ducts.


Links: Endoderm | Mouse Development

Development

Stage 13

stage 13 embryo

The images below link to larger cross-sections of the mid-embryonic period (end week 4) stage 13 embryo starting just above the level of the liver and then in sequence through the liver to the level of the stomach. Note the relative position of the liver with respect to the abdominal cavity, the gall bladder and the heart.

The transverse septum differentiates to form the hepatic diverticulum and the hepatic primordium, these two structures together will go on to form different components of the mature liver and gall bladder. At this stage large vascular channels can be seen coursing through the liver primordium.

Stage 13 (serial labeled images)
Stage 13 image 073.jpg Stage 13 image 074.jpg Stage 13 image 075.jpg Stage 13 image 076.jpg Stage 13 image 077.jpg Stage 13 image 078.jpg
D3L D4L D5L D6L D7L E1L
Stage 13 image 097.jpg Stage 13 image 098.jpg
G6L G7L
Links: Carnegie stage 13 - serial sections | Embryo Serial Sections | Embryo Carnegie stage 13 Movies

Stage 22

Virtual Slide Features - Stage 22 Liver
Stage 22 image 034.jpg Virtual Slide - Stage 22 Liver and Ductus Venosus      All Virtual Slides

The links shown in the table below are to specific features shown on the Human embryo (stage 22) Liver and Ductus Venosus virtual slide.

Clicking the text will open the slide at a detailed view with the structure generally located in the centre of the view. The slide then can also be zoomed out from the set magnification using the controls in the upper left or the mouse.

Use your browser back button to return to this table.

You can also make your own selected feature view.
  1. Set the virtual slide to the region and zoom of interest.
  2. Click the Permalink (lower righthand corner).
  3. Then bookmark in your browser, or copy the web address.

See also Permalink help

Cardiovascular Liver Endocrine Musculoskeletal Neural Gastrointestinal

stomach (pylorus)

The images below link to larger cross-sections of the end of the embryonic period (week 8) stage 22 embryo starting just above the level of the liver and then in sequence through the entire liver. (Note the sections are viewed from below, LR axis is reversed)

The rapidly developing liver also forms a visible surface bulge on the embryo directly under the heart bulge. The liver now occupies the entire ventral body cavity with parts of the gastrointestinal tract and urinary system "embedded" within its structure. Note in this image the large central ductus venosus.

Stage 22L serial labeled images
Stage 22 image 080.jpg Stage 22 image 081.jpg Stage 22 image 082.jpg Stage 22 image 083.jpg Stage 22 image 084.jpg
E3L E4L E5L E6L E7L
Stage 22 image 085.jpg Stage 22 image 086.jpg Stage 22 image 087.jpg Stage 22 image 088.jpg Stage 22 image 089.jpg
F1L F2L F3L F4L F5L
Links: Carnegie stage 22 - serial sections | Embryo Serial Sections | Embryo Carnegie stage 22 Movies

Selected Stage 22 Images

Stage 22 image 131.jpg E3 Overview of liver region for selected high power views shown below. Note the position and size of the developing liver spanning the entire abdomen and within the liver the large central ductus venosus.
Stage 22 image 181.jpg E4 Central veins of liver. Radiating appearance of hepatic sinusoids. unlabeled version
Stage 22 image 182.jpg E5 Central vein with endothelial lining, containing nucleated erythrocytes, fetal red blood cells. The fetal liver has an important haemopoietic role. unlabeled version

Week 9

Human liver week 9.jpg

Paraffin-embedded sections of human embryonic liver at 9 weeks (GA 11 weeks).[10]

  • A - (Stain - Haematoxylin Eosin)
  • B, C - Alpha-Fetoprotein (AFP)
  • D, G - Cytokeratin 18 (CK18)
  • E, H - Cytokeratin 19 (CK19)
  • F, I - Cytokeratin 7 (CK7)

Ductal Plate

The ductal plate is a primitive biliary epithelium which develops in mesenchyme adjacent to portal vein branches (periportal hepatoblasts). During liver development it is extensively reorganised (ductal plate remodelling) within the developing liver to form the intrahepatic bile ducts (IHBD). If remodelling does not occur, leading to excess of embryonic bile duct structures in the portal tract, these developmental abnormalities are described as "ductal plate malformation" (DPM).

Ductal Plate Malformations

  • Interlobular bile ducts - autosomal recessive polycystic kidney disease
  • Smaller interlobular ducts - von Meyenburg complexes
  • Larger intrahepatic bile ducts - Caroli's disease

Bile Secretion

The epithelial cells that line the bile ducts are called cholangiocytes.

The pathway below describes the production and passage of bile for final excretion into the duodenum:

  1. hepatocytes produce bile
  2. secreted into bile canaliculi
  3. connected to intrahepatic bile ducts
  4. intrahepatic bile ducts connect to the hepatic duct
  5. then the cystic duct for storage in the gallbladder
  6. then the common bile duct into the duodenum

The term extrahepatic bile ducts (EHBDs) is used to describe the hepatic, cystic, and common bile ducts.

The developing bile ducts express VEGF while hepatoblasts express angiopoietin-1, these two signals are thought to regulate arterial vasculogenesis and remodeling of the hepatic artery respectively.[11]

Liver Blood Flow

Liver structure cartoon.jpg

Dual blood supply of the liver merges upon entry into the liver lobule at the portal field.

  1. branches of the portal vein
  2. branches of the hepatic artery

The blood flows along the sinusoid and exits at the central vein.

Hepatocytes

Adult Liver sinusoid structure

These are the adult functional cells forming the majority of the liver (80% of the cells).

Many different functions including:

  • Storage of substances including glucose (as glycogen), vitamin A (possibly in specialized adipocytes), vitamin B12, folic acid and iron.
  • Lipid Turnover synthesis of plasmalipoproteins
  • Plasma Protein Synthesis albumin, alpha and beta globulins, prothrombin, fibrinogen
  • Metabolism fat soluble compounds (drugs, insecticides), steroid hormones turnover
  • Secretion bile (about 1 litre/day)

Kupffer Cells

Kupffer Cells are a population of tissue macrophages found in the lumen of hepatic sinusoids, their role is endocytic against blood-borne materials entering the liver.

Primordial (primitive) macrophages arise in the yolk sac and then differentiate into fetal macrophages, either of these enter the blood and migrate into the developing liver.[12]


Kupffer Cells image


Search PubMed: Kupffer cell development

Liver Associated Vessels

Gray0475.jpg

Liver ventral surface and associated veins (human embryo, 24-25 days, after His.)

  • ductus venosus - shunts approximately half the umbilical vein blood flow directly to the inferior vena cava.
  • portal vein - carries blood from the gastrointestinal tract and spleen to the liver.
  • left umbilical vein - carries oxygenated blood from the placenta to the embryo/fetus.
  • right umbilical vein - vessel degenerates leaving a single (left) umbilical vein.
  • vena revehens - veins from the sinusoid vessels in the liver to the inferior vena cava, that later develop into the hepatic veins.

Adult Liver Transplants

Histology

Liver animated cartoon.gif

The Liver Lobule

Adult liver Portal Triad

Liver histology 005.jpg


Links: Liver Histology

Abnormalities

Congenital absence of the portal vein (CAPV) - a rare abnormality where the intestinal and splenic venous drainage bypass the liver and drain directly into the systemic veins through various porto-systemic shunts.

Links: Gastrointestinal Tract - Abnormalities

References

  1. Peter S Vestentoft, Peter Jelnes, Branden M Hopkinson, Ben Vainer, Kjeld Møllgård, Bjørn Quistorff, Hanne C Bisgaard Three-dimensional reconstructions of intrahepatic bile duct tubulogenesis in human liver. BMC Dev. Biol.: 2011, 11;56 PubMed 21943389
  2. Ewa Wandzioch, Kenneth S Zaret Dynamic signaling network for the specification of embryonic pancreas and liver progenitors. Science: 2009, 324(5935);1707-10 PubMed 19556507 | PMC2771431 | Science
  3. Ewa Wandzioch, Kenneth S Zaret Dynamic signaling network for the specification of embryonic pancreas and liver progenitors. Science: 2009, 324(5935);1707-10 PubMed 19556507
  4. John G Archie, Julianne S Collins, Robert Roger Lebel Quantitative standards for fetal and neonatal autopsy. Am. J. Clin. Pathol.: 2006, 126(2);256-65 PubMed 16891202
  5. G Godlewski, R Gaubert-Cristol, S Rouy, M Prudhomme Liver development in the rat and in man during the embryonic period (Carnegie stages 11-23). Microsc. Res. Tech.: 1997, 39(4);314-27 PubMed 9407542
  6. G Godlewski, R Gaubert-Cristol, S Rouy, M Prudhomme Liver development in the rat during the embryonic period (Carnegie stages 15-23). Acta Anat (Basel): 1997, 160(3);172-8 PubMed 9718390
  7. Martin Lhuaire, Romain Tonnelet, Yohann Renard, Tullio Piardi, Daniele Sommacale, Fabrice Duparc, Marc Braun, Marc Labrousse Developmental anatomy of the liver from computerized three-dimensional reconstructions of four human embryos (from Carnegie stage 14 to 23). Ann. Anat.: 2015, 200;105-113 PubMed 25866917 | Ann Anat.
  8. Karen Pauwelyn, Philip Roelandt, Tineke Notelaers, Pau Sancho-Bru, Johan Fevery, Catherine M Verfaillie Culture of mouse embryonic stem cells with serum but without exogenous growth factors is sufficient to generate functional hepatocyte-like cells. PLoS ONE: 2011, 6(8);e23096 PubMed 21829697 | PLoS One.
  9. Kaufman and Bard, The Anatomical Basis of Mouse Development 1999 Academic Press
  10. Galit Tzur, Ariel Israel, Asaf Levy, Hila Benjamin, Eti Meiri, Yoel Shufaro, Karen Meir, Elina Khvalevsky, Yael Spector, Nathan Rojansky, Zvi Bentwich, Benjamin E Reubinoff, Eithan Galun Comprehensive gene and microRNA expression profiling reveals a role for microRNAs in human liver development. PLoS ONE: 2009, 4(10);e7511 PubMed 19841744 | PMC2760133 | PLoS
  11. James M Crawford Development of the intrahepatic biliary tree. Semin. Liver Dis.: 2002, 22(3);213-26 PubMed 12360416
  12. Makoto Naito, Go Hasegawa, Yusuke Ebe, Takashi Yamamoto Differentiation and function of Kupffer cells. Med Electron Microsc: 2004, 37(1);16-28 PubMed 15057601
  13. Ruchi Sharma, Sebastian Greenhough, Claire N Medine, David C Hay Three-dimensional culture of human embryonic stem cell derived hepatic endoderm and its role in bioartificial liver construction. J. Biomed. Biotechnol.: 2010, 2010;236147 PubMed 20169088 | PMC2821762


Reviews

Takahiro Nakamura, Katsuya Sakai, Toshikazu Nakamura, Kunio Matsumoto Hepatocyte growth factor twenty years on: Much more than a growth factor. J. Gastroenterol. Hepatol.: 2011, 26 Suppl 1;188-202 PubMed 21199531

Hisami Ando Embryology of the biliary tract. Dig Surg: 2010, 27(2);87-9 PubMed 20551648

Janet W C Kung, Ian S Currie, Stuart J Forbes, James A Ross Liver development, regeneration, and carcinogenesis. J. Biomed. Biotechnol.: 2010, 2010;984248 PubMed 20169172

Karim Si-Tayeb, Frédéric P Lemaigre, Stephen A Duncan Organogenesis and development of the liver. Dev. Cell: 2010, 18(2);175-89 PubMed 20159590

John Le Lay, Klaus H Kaestner The Fox genes in the liver: from organogenesis to functional integration. Physiol. Rev.: 2010, 90(1);1-22 PubMed 20086072

T Roskams, V Desmet Embryology of extra- and intrahepatic bile ducts, the ductal plate. Anat Rec (Hoboken): 2008, 291(6);628-35 PubMed 18484608


Articles

Vincenzo Cardinale, Yunfang Wang, Guido Carpino, Gemma Mendel, Gianfranco Alpini, Eugenio Gaudio, Lola M Reid, Domenico Alvaro The biliary tree--a reservoir of multipotent stem cells. Nat Rev Gastroenterol Hepatol: 2012, 9(4);231-40 PubMed 22371217

Joshua R Friedman, Klaus H Kaestner On the origin of the liver. J. Clin. Invest.: 2011, 121(12);4630-3 PubMed 22105167

Rodolphe Carpentier, Regina Español Suñer, Noémi van Hul, Janel L Kopp, Jean-Bernard Beaudry, Sabine Cordi, Aline Antoniou, Peggy Raynaud, Sébastien Lepreux, Patrick Jacquemin, Isabelle A Leclercq, Maike Sander, Frédéric P Lemaigre Embryonic ductal plate cells give rise to cholangiocytes, periportal hepatocytes, and adult liver progenitor cells. Gastroenterology: 2011, 141(4);1432-8, 1438.e1-4 PubMed 21708104


Search Pubmed

Search Bookshelf Liver Development

Search Pubmed Now: Liver Development | Embryonic Liver Development

Additional Images

Historic

Mall FP. A Study of the Structural Unit of the Liver (1906) Amer. J. of Anat. 5:227-308.

Glossary Links

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Cite this page: Hill, M.A. (2016) Embryology Gastrointestinal Tract - Liver Development. Retrieved February 8, 2016, from https://embryology.med.unsw.edu.au/embryology/index.php/Gastrointestinal_Tract_-_Liver_Development

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