Talk:Gastrointestinal Tract - Stomach Development: Difference between revisions
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==2009== | |||
===Sfrp controls apicobasal polarity and oriented cell division in developing gut epithelium.=== | |||
PLoS Genet. 2009 Mar;5(3):e1000427. Epub 2009 Mar 20. | PLoS Genet. 2009 Mar;5(3):e1000427. Epub 2009 Mar 20. | ||
Matsuyama M, Aizawa S, Shimono A. | Matsuyama M, Aizawa S, Shimono A. | ||
Vertebrate Body Plan, Center for Developmental Biology, RIKEN Kobe, Minatojima-Minami, Kobe, Japan. | Vertebrate Body Plan, Center for Developmental Biology, RIKEN Kobe, Minatojima-Minami, Kobe, Japan. | ||
Abstract | Abstract | ||
Epithelial tubular morphogenesis leading to alteration of organ shape has important physiological consequences. However, little is known regarding the mechanisms that govern epithelial tube morphogenesis. Here, we show that inactivation of Sfrp1 and Sfrp2 leads to reduction in fore-stomach length in mouse embryos, which is enhanced in the presence of the Sfrp5 mutation. In the mono-cell layer of fore-stomach epithelium, cell division is normally oriented along the cephalocaudal axis; in contrast, orientation diverges in the Sfrps-deficient fore-stomach. Cell growth and apoptosis are not affected in the Sfrps-deficient fore-stomach epithelium. Similarly, cell division orientation in fore-stomach epithelium diverges as a result of inactivation of either Stbm/Vangl2, an Fz/PCP component, or Wnt5a. These observations indicate that the oriented cell division, which is controlled by the Fz/PCP pathway, is one of essential components in fore-stomach morphogenesis. Additionally, the small intestine epithelium of Sfrps compound mutants fails to maintain proper apicobasal polarity; the defect was also observed in Wnt5a-inactivated small intestine. In relation to these findings, Sfrp1 physically interacts with Wnt5a and inhibits Wnt5a signaling. We propose that Sfrp regulation of Wnt5a signaling controls oriented cell division and apicobasal polarity in the epithelium of developing gut. | Epithelial tubular morphogenesis leading to alteration of organ shape has important physiological consequences. However, little is known regarding the mechanisms that govern epithelial tube morphogenesis. Here, we show that inactivation of Sfrp1 and Sfrp2 leads to reduction in fore-stomach length in mouse embryos, which is enhanced in the presence of the Sfrp5 mutation. In the mono-cell layer of fore-stomach epithelium, cell division is normally oriented along the cephalocaudal axis; in contrast, orientation diverges in the Sfrps-deficient fore-stomach. Cell growth and apoptosis are not affected in the Sfrps-deficient fore-stomach epithelium. Similarly, cell division orientation in fore-stomach epithelium diverges as a result of inactivation of either Stbm/Vangl2, an Fz/PCP component, or Wnt5a. These observations indicate that the oriented cell division, which is controlled by the Fz/PCP pathway, is one of essential components in fore-stomach morphogenesis. Additionally, the small intestine epithelium of Sfrps compound mutants fails to maintain proper apicobasal polarity; the defect was also observed in Wnt5a-inactivated small intestine. In relation to these findings, Sfrp1 physically interacts with Wnt5a and inhibits Wnt5a signaling. We propose that Sfrp regulation of Wnt5a signaling controls oriented cell division and apicobasal polarity in the epithelium of developing gut. | ||
PMID 19300477 | |||
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== WWW Links == | == WWW Links == | ||
Indiana University animation showing [http://www.indiana.edu/~anat550/gianim/sdo/sdo.html Development of the Stomach, Omenta and Duodenum ]Discussion of the development of the stomach from the foregut, the omenta development from the mesenteries, and the rotational movements of the stomach and duodenum.(approx. 2 minutes) | Indiana University animation showing [http://www.indiana.edu/~anat550/gianim/sdo/sdo.html Development of the Stomach, Omenta and Duodenum ]Discussion of the development of the stomach from the foregut, the omenta development from the mesenteries, and the rotational movements of the stomach and duodenum.(approx. 2 minutes) | ||
==Introduction== | |||
This section of notes gives an overview of how the stomach and duodenum develops. The GIT is best imagined as a simple tube, the upper part being the foregut diverticulum, which is further divided into oesophagus and stomach. | |||
During week 4 where the stomach will form the tube begins to dilate, forming an enlarged lumen in the tube. Dorsal border grows more rapidly than ventral, which establishes the greater curvature of the stomach. A second rotation (of 90 degrees) occurs on the longitudinal axis establishing the adult orientation of the stomach. | |||
stomach | |||
* glandular/proventricular/pyloric stenosis | |||
* fundus/pyloric antrum | |||
* pyloric sphincter | |||
[http://embryology.med.unsw.edu.au/Notes/git10.htm original page] | |||
==Greater Omentum== | |||
The greater omentum hangs like an apron over the small intestine and transverse colon. It begins attacted to the inferior end of the stomach as a fold of the dorsal mesogastrium which later fuses to form the structure we recognise anatomically. The figure below shows a lateral view of this process comparing the early second trimester arrangement with the newborn structure. (More? GIT Folding) | |||
==Duodenum/Pancreas Rotation== | |||
After the stomach the initial portion of the GIT tube is the duodenum which initially lies in the midline within the peritoneal cavity, but then (along with the attached pancreas) undergoes rotation to become a retroperitoneal structure. (More? GIT Folding) | |||
The diagram below shows this rotation with spinal cord at the top, vertebral body then dorsal aorta then pertioneal wall and cavity. | |||
==Stomach Hormonal Development== | |||
The gastrointestinal tract has its own complex entero-endocrine system (enterohormones) that regulates many regional tract functions. | |||
Cells within the stomach express a range of peptide hormones known to regulate a range of gastric functions including secretion of digestive enzymes, mucous and the movement of the luminal contents. The list below shows the earliest detectible presence of specific hormone-containing cells in regions of the developing human stomach. | |||
8 weeks - Gastrin containing cells in stomach antrum. Somatostatin cells in both the antrum and the fundus. | |||
10 weeks - Glucagon containing cells in stomach fundus. | |||
11 weeks - Serotonin containing cells in both the antrum and the fundus. | |||
(Data: Stein BA, Buchan AM, Morris J, Polak JM. The ontogeny of regulatory peptide-containing cells in the human fetal stomach: an immunocytochemical study. J Histochem Cytochem. 1983 Sep;31(9):1117-25.) | |||
Other gut peptides: cholecystokinin (CCK), pancreatic polypeptide, peptide YY, glucagon-like peptide-1 (GLP-1), oxyntomodulin (increase satiety and decrease food intake) and ghrelin |
Revision as of 00:56, 14 February 2012
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Cite this page: Hill, M.A. (2024, April 25) Embryology Gastrointestinal Tract - Stomach Development. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Talk:Gastrointestinal_Tract_-_Stomach_Development |
2009
Sfrp controls apicobasal polarity and oriented cell division in developing gut epithelium.
PLoS Genet. 2009 Mar;5(3):e1000427. Epub 2009 Mar 20.
Matsuyama M, Aizawa S, Shimono A.
Vertebrate Body Plan, Center for Developmental Biology, RIKEN Kobe, Minatojima-Minami, Kobe, Japan.
Abstract Epithelial tubular morphogenesis leading to alteration of organ shape has important physiological consequences. However, little is known regarding the mechanisms that govern epithelial tube morphogenesis. Here, we show that inactivation of Sfrp1 and Sfrp2 leads to reduction in fore-stomach length in mouse embryos, which is enhanced in the presence of the Sfrp5 mutation. In the mono-cell layer of fore-stomach epithelium, cell division is normally oriented along the cephalocaudal axis; in contrast, orientation diverges in the Sfrps-deficient fore-stomach. Cell growth and apoptosis are not affected in the Sfrps-deficient fore-stomach epithelium. Similarly, cell division orientation in fore-stomach epithelium diverges as a result of inactivation of either Stbm/Vangl2, an Fz/PCP component, or Wnt5a. These observations indicate that the oriented cell division, which is controlled by the Fz/PCP pathway, is one of essential components in fore-stomach morphogenesis. Additionally, the small intestine epithelium of Sfrps compound mutants fails to maintain proper apicobasal polarity; the defect was also observed in Wnt5a-inactivated small intestine. In relation to these findings, Sfrp1 physically interacts with Wnt5a and inhibits Wnt5a signaling. We propose that Sfrp regulation of Wnt5a signaling controls oriented cell division and apicobasal polarity in the epithelium of developing gut.
PMID 19300477
File:Stomach.jpg | |
During week 4 where the stomach will form the tube begins to dilate, forming an enlarged lumen in the tube. Dorsal border grows more rapidly than ventral, which establishes the greater curvature of the stomach. A second rotation (of 90 degrees) occurs on the longitudinal axis establishing the adult orientation of the stomach.
Stage 13/14 Stomach
File:St1314sm.gif | File:D2st13stom.gif | File:D3lst13stom.gif | File:D4st13stom.gif |
View through osophageal pyloric region at top of stomach.(base of R. and L. lung buds) | Beginning of stomach rotation. Broad dorsal mesogastrium, narrow ventral mesogastrium. Cavity beneath stomach is the omentum bursa. | Section through the body of the stomach. Dorsal mesogastrium beneath the omentum bursa will form greater omentum. | |
File:D5st13stom.gif | File:D6st13stom.gif | File:D7st13stom.gif | |
Section through the body of the stomach. | Section at the stomach duodenal junction. |
Stage 22 Stomach
File:St22hum.gif | File:E6lst22stom.gif | File:E7lst22stom.gif |
Note thick muscular wall of stomach body and change in lumen shape between pyloris and duodenum. | ||
File:F1lst22stom.gif | File:F2lst22stom.gif | File:F3lst22stom.gif |
File:F4lst22stom.gif | File:F5lst22stom.gif | |
Greater Omentum
The greater omentum hangs like an apron over the small intestine and transverse colon. It begins attacted to the inferior end of the stomach as a fold of the dorsal mesogastrium which later fuses to form the structure we recognise anatomically. The figure below shows a lateral view of this process comparing the early second trimester arrangement with the newborn structure. (More? [git12.htm GIT Folding])
Stomach Development Movies
File:Stomrot.jpg[../Movies/larsen/stomrot.mov Stomach Rotation] (326 Kb) | File:Stomrot2.jpg[../Movies/larsen/stomrot2.mov Stomach Rotation ]large version (620 Kb) |
File:LessersacA.jpg[../Movies/larsen/lessersacA.mov Lesser Sac ]superior view (104 Kb) | File:LessersacB.jpg[../Movies/larsen/lessersacB.mov Lesser Sac] ventrolateral view (408 Kb) |
3D Model Movies
The following are links to 3D reconstruction animations of serial images of the gastrointestinal tract at an early and late embryonic stage. (More? [3dmodel.htm 3D Model Movies])
Stage 13/14 Embryo: [../Movies/GIT3dmodel.htm Gastrointestinal Tract]
Stage 22 Embryo: [../Movies/GIT3dmodelst22.htm Gastrointestinal Tract]
Adult Stomach Position
File:Stomach-position.jpg | Movie of anatomical position of the erect adult stomach position on filling, based upon historic drawings.
Quicktime: [../Movies/git/adult_stomach_position.mov adult_stomach_position.mov (36 Kb)] |
Abnormalities
- Congenital hypertrophic pyloric stenosis
- duodenal atresia
- duodenal stenosis
WWW Links
Indiana University animation showing Development of the Stomach, Omenta and Duodenum Discussion of the development of the stomach from the foregut, the omenta development from the mesenteries, and the rotational movements of the stomach and duodenum.(approx. 2 minutes)
Introduction
This section of notes gives an overview of how the stomach and duodenum develops. The GIT is best imagined as a simple tube, the upper part being the foregut diverticulum, which is further divided into oesophagus and stomach.
During week 4 where the stomach will form the tube begins to dilate, forming an enlarged lumen in the tube. Dorsal border grows more rapidly than ventral, which establishes the greater curvature of the stomach. A second rotation (of 90 degrees) occurs on the longitudinal axis establishing the adult orientation of the stomach.
stomach
- glandular/proventricular/pyloric stenosis
- fundus/pyloric antrum
- pyloric sphincter
Greater Omentum
The greater omentum hangs like an apron over the small intestine and transverse colon. It begins attacted to the inferior end of the stomach as a fold of the dorsal mesogastrium which later fuses to form the structure we recognise anatomically. The figure below shows a lateral view of this process comparing the early second trimester arrangement with the newborn structure. (More? GIT Folding)
Duodenum/Pancreas Rotation
After the stomach the initial portion of the GIT tube is the duodenum which initially lies in the midline within the peritoneal cavity, but then (along with the attached pancreas) undergoes rotation to become a retroperitoneal structure. (More? GIT Folding)
The diagram below shows this rotation with spinal cord at the top, vertebral body then dorsal aorta then pertioneal wall and cavity.
Stomach Hormonal Development
The gastrointestinal tract has its own complex entero-endocrine system (enterohormones) that regulates many regional tract functions.
Cells within the stomach express a range of peptide hormones known to regulate a range of gastric functions including secretion of digestive enzymes, mucous and the movement of the luminal contents. The list below shows the earliest detectible presence of specific hormone-containing cells in regions of the developing human stomach.
8 weeks - Gastrin containing cells in stomach antrum. Somatostatin cells in both the antrum and the fundus.
10 weeks - Glucagon containing cells in stomach fundus.
11 weeks - Serotonin containing cells in both the antrum and the fundus.
(Data: Stein BA, Buchan AM, Morris J, Polak JM. The ontogeny of regulatory peptide-containing cells in the human fetal stomach: an immunocytochemical study. J Histochem Cytochem. 1983 Sep;31(9):1117-25.)
Other gut peptides: cholecystokinin (CCK), pancreatic polypeptide, peptide YY, glucagon-like peptide-1 (GLP-1), oxyntomodulin (increase satiety and decrease food intake) and ghrelin