Cardiovascular System - Blood Vessel Development
|Embryology - 10 Oct 2015 Translate|
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- 1 Introduction
- 2 Some Recent Findings
- 3 Endothelial Progenitors
- 4 Vessel Specification
- 5 Vascular Endothelial Growth Factor
- 6 Regulators of Growth
- 7 Histology
- 8 Capillaries
- 9 Cardiac Blood Vessels
- 10 References
- 11 Terms
- 12 External Links
- 13 Glossary Links
Blood develops initially within the core of "blood islands" in the mesoderm. During development, there follows a series of "relocations" of the stem cells to different organs within the embryo. In the adult, these stem cells are located in the bone marrow. At the time when blood first forms, there are no bones!
Angioblasts initially form small cell clusters (blood islands) within the embryonic and extraembryonic mesoderm. These blood islands extend and fuse together making a primordial vascular network. Within these islands the peripheral cells form endothelial cells while the core cells form blood cells (haemocytoblasts).
Recent work has shown that the formation of the initial endothelial tube is by a process of coalescence of cellular vacuoles within the developing endothelial cells, which fuse together without cytoplasmic mixing to form the blood vessel lumen.
- Cardiovascular Links: Introduction | Heart Tutorial | Lecture - Early Vascular | Lecture - Heart | Movies | Coronary Circulation | Heart Valve | Heart Rate | Blood | Blood Vessel | Blood Vessel Histology | Cardiac Muscle Histology | Lymphatic | Spleen | Stage 22 | Abnormalities | OMIM | ECHO Meeting | Category:Cardiovascular
Some Recent Findings
|More recent papers|
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.
I D Molodtsova, D S Medvedev, V O Poliakova, N S Lin'kova, G I Gurko [INFLUENCE OF MILLIMETER-WAVE ELECTROMAGNETIC EMISSION ON NITRIC OXIDE SYNTHESIS DURING VESSEL ENDOTHELIUM AGING IN VITRO]. Adv Gerontol: 2015, 28(1);68-71 PubMed 26390613
Selahattin Kıyan, Yiğit Uyanıkgil, Yusuf Ali Altuncı, Türker Çavuşoğlu, Emel Öykü Çetin Uyanıkgil, Fatih Karabey Investigation of acute effects of Hypericum perforatum (St. John's Wort-Kantaron) treatment in experimental thermal burns and comparison with silver sulfadiazine treatment. Ulus Travma Acil Cerrahi Derg: 2015, 21(5);323-36 PubMed 26388268
R G Ahmed, M Abdel-Latif, Emad A Mahdi, Khalid A El-Nesr Immune stimulation improves endocrine and neural fetal outcomes in a model of maternofetal thyrotoxicosis. Int. Immunopharmacol.: 2015; PubMed 26388190
Xiaoli Zhang, Ruihua Liu, Zhongxue Su, Yuecun Zhang, Wenfang Zhang, Xinyu Liu, Fuwu Wang, Yuji Guo, Chuangang Li, Jing Hao Immunohistochemical Study of Expression of Sohlh1 and Sohlh2 in Normal Adult Human Tissues. PLoS ONE: 2015, 10(9);e0137431 PubMed 26375665
Hakan Sirinoglu, Özlem Tuğçe Çilingir, Ozhan Çelebiler, Feriha Ercan, Ayhan Numanoglu The Effect of Liquid Nitrogen on Bone Graft Survival. Facial Plast Surg: 2015, 31(4);401-410 PubMed 26372716
Recent work has shown that the formation of the initial endothelial tube is by a process of coalescence of cellular vacuoles within the developing endothelial cells, which fuse together without cytoplasmic mixing to form the blood vessel lumen. 
Endothelial Tube Formation
The following data is from a recent review.
|Shh||Loss of Shh results in lack of arterial identity in zebrafish. Shh acts upstream of VEGF.|
|VEGF||VEGF acts downstream of Shh signaling to activate Notch via the PLCγ/ERK pathway in zebrafish. Mutant mice expressing only VEGF188 lack arterial differentiation.|
|Nrp1||Null mice display impaired arterial differentiation. Nrp1 is involved in a positive feedback loop of VEGF signaling.|
|Notch||Notch acts downstream of Shh and VEGF signaling in zebrafish. Notch1; Notch4 mutant mice have abnormal vascular development.|
|Dll4||Null mice lack arterial specification.|
|Dll1||Null mice fail to maintain arterial identity.|
|Hey1/2 (Grl)||Null mice lack arterial specification. Lack of grl in zebrafish results in loss of arterial specification.|
|Foxc1/c2||Foxc1; Foxc2 mutant mice lack arterial specification. Foxc1 and Foxc2 directly regulate Dll4 and Hey2 expression. Foxc1 and Foxc2 are also involved in lymphatic vessel development.|
|Sox7/18||Lack of Sox7/18 results in loss of arterial identity in zebrafish.|
|Snrk-1||Snrk-1 acts downstream or parallel to Notch signaling in zebrafish.|
|Dep1||Dep1 acts upstream of PI3K in arterial specification in zebrafish.|
|Crlr||Shh regulates VEGF activity by controlling crlr expression in zebrafish.|
|EphrinB2||Null mice lack boundaries between arteries and veins. EphrinB2 is involved in lymphatic vascular remodeling and maturation.|
|COUP-TFII||COUP-TFII suppresses arterial cell fate by inhibiting Nrp1 and Notch. COUP-TFII also interacts with Prox1 to regulate lymphatic gene expression.|
|EphB4||Null mice lack boundaries between arteries and veins.|
|Sox18||Null mice fail to specify lymphatic endothelial cells. Sox18 induces Prox1 expression.|
|Prox1||Prox1 induces lymphatic markers and maintains lymphatic cell identity.|
Vascular Endothelial Growth Factor
Growing blood vessels follow a gradient generated by tagret tissues/regions of Vascular Endothelial Growth Factor (VEGF) to establish a vascular bed. Recent findings suggest that Notch signaling acts as an inhibitor for this system, preventing sprouting of blood vessels.
Notch is a transmembrane receptor protein involved in regulating cell differentiation in many developing systems.
Notch and yolk sac blood vessels model
Regulators of Growth
The following data is from a review article on ovary vascular development.
Stimulators of Angiogenisis
Inhibitors of Angiogenisis
Vein Light Microscopy
The entire developing and adult cardiovascular system (blood vessels and heart) is lined by a simple squamous epithelium. (Stain - Haematoxylin Eosin)
Cardiac Blood Vessels
Earliest vessels in the heart wall develop subepicardially (beneath the outside surface of the heart) near the apex at Carnegie stage 15, which then extends centripetally and at stage 17 coronary arterial stems communicate with the aortic lumen.
- Jason E Fish, Joshua D Wythe The Molecular Regulation of Arteriovenous Specification and Maintenance. Dev. Dyn.: 2015; PubMed 25641373
- Tsutomu Kume Specification of arterial, venous, and lymphatic endothelial cells during embryonic development. Histol. Histopathol.: 2010, 25(5);637-46 PubMed 20238301 | PMC2899674
- Per Wasteson, Bengt R Johansson, Tomi Jukkola, Silke Breuer, Levent M Akyürek, Juha Partanen, Per Lindahl Developmental origin of smooth muscle cells in the descending aorta in mice. Development: 2008, 135(10);1823-32 PubMed 18417617
- Frances A High, Min Min Lu, Warren S Pear, Kathleen M Loomes, Klaus H Kaestner, Jonathan A Epstein Endothelial expression of the Notch ligand Jagged1 is required for vascular smooth muscle development. Proc. Natl. Acad. Sci. U.S.A.: 2008, 105(6);1955-9 PubMed 18245384
- Morayma Reyes, Arkadiusz Dudek, Balkrishna Jahagirdar, Lisa Koodie, Paul H Marker, Catherine M Verfaillie Origin of endothelial progenitors in human postnatal bone marrow. J. Clin. Invest.: 2002, 109(3);337-46 PubMed 11827993
- Jessica N Copeland, Yi Feng, Naveen K Neradugomma, Patrick E Fields, Jay L Vivian Notch signaling regulates remodeling and vessel diameter in the extraembryonic yolk sac. BMC Dev. Biol.: 2011, 11;12 PubMed 21352545 | BMC Dev Biol.
- H G Augustin Vascular morphogenesis in the ovary. Baillieres Best Pract Res Clin Obstet Gynaecol: 2000, 14(6);867-82 PubMed 11141338
- Benoit Detry, Françoise Bruyère, Charlotte Erpicum, Jenny Paupert, Françoise Lamaye, Catherine Maillard, Bénédicte Lenoir, Jean-Michel Foidart, Marc Thiry, Agnès Noël Digging deeper into lymphatic vessel formation in vitro and in vivo. BMC Cell Biol.: 2011, 12;29 PubMed 21702933 | PMC3141733 | BMC Cell Biol.
- K Turner, V Navaratnam The positions of coronary arterial ostia. Clin Anat: 1996, 9(6);376-80 PubMed 8915616
Jason E Fish, Joshua D Wythe The Molecular Regulation of Arteriovenous Specification and Maintenance. Dev. Dyn.: 2015; PubMed 25641373
A J Davidson, L I Zon Turning mesoderm into blood: the formation of hematopoietic stem cells during embryogenesis. Curr. Top. Dev. Biol.: 2000, 50;45-60 PubMed 10948449
Kathleen E McGrath, Anne D Koniski, Jeffrey Malik, James Palis Circulation is established in a stepwise pattern in the mammalian embryo. Blood: 2003, 101(5);1669-76 PubMed 12406884
Click on the listed keywords below (used to search the external database) the most current references on Medline will be displayed.
- angioblasts stem cells in blood islands generating endothelial cells
- angiogenesis the formation of blood vessels also called vasculogenesis in the embryo
- blood islands earliest sites of blood vessel and blood cell formation, seen mainly on yolk sac chorion
- vascular endothelial growth factor (VEGF) protein growth factor family that stimulates blood vessel growth, a similar factor can be found in the placenta (PIGF).
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Cite this page: Hill, M.A. (2015) Embryology Cardiovascular System - Blood Vessel Development. Retrieved October 10, 2015, from https://embryology.med.unsw.edu.au/embryology/index.php/Cardiovascular_System_-_Blood_Vessel_Development
- © Dr Mark Hill 2015, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G