Early pattern of differentiation in the human pancreas

Early pattern of differentiation in the human pancreas. M Polak , L Bouchareb-Banaei , R Scharfmann and P Czernichow Institut National de la Santé et de la Recherche Médicale (INSERM) U457, Department of Pediatric Endocrinology and Diabetes, Hôpital Robert Debré, Paris, France. michel.polak@rdb.ap-h...

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Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2000-02, Vol.49 (2), p.225-232
Hauptverfasser: POLAK, M, BOUCHAREB-BANAEI, L, SCHARFMANN, R, CZERNICHOW, P
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creator POLAK, M
BOUCHAREB-BANAEI, L
SCHARFMANN, R
CZERNICHOW, P
description Early pattern of differentiation in the human pancreas. M Polak , L Bouchareb-Banaei , R Scharfmann and P Czernichow Institut National de la Santé et de la Recherche Médicale (INSERM) U457, Department of Pediatric Endocrinology and Diabetes, Hôpital Robert Debré, Paris, France. michel.polak@rdb.ap-hop-paris.fr Abstract In the early human embryonic/fetal pancreas, we studied 1) the ontogenetic pattern of the endocrine cells and the evolution of the endocrine mass, and 2) the morphogenetic pattern of development and, more precisely, the complex relationship of the epithelial mass with the surrounding mesenchyme. We studied 15 pancreases between 7 and 11 weeks of development (WD) by double immunohistochemistry. Epithelial cells in these pancreatic anlage were detected by cytokeratin staining, and differentiated endocrine cells were detected by insulin, glucagon, somatostatin, and pancreatic polypeptide staining. Proliferation was quantified using a nuclear marker, the Ki-67 antibody. At this early stage, the pancreas is made up of an epithelial mass composed of central ducts intermingled with a loose mesenchyme and peripheral ducts surrounded by a dense peripancreatic mesenchyme. Hormone-containing cells appear in the epithelium at 8 WD. Newly differentiated endocrine cells coexpress insulin, glucagon, and somatostatin; endocrine differentiation starts within the central ducts of the epithelial mass, at a distance from the dense peripancreatic surrounding mesenchyme. The fraction of the primitive endocrine cells undergoing proliferation is low (5% of the insulin cells at 8 WD, 3% at 11 WD), which is in favor of massive differentiation as the major mechanism for increasing endocrine mass. By contrast, the nonendocrine epithelial cells have a higher rate of proliferation; the epithelial cells in contact with the dense peripancreatic surrounding mesenchyme show more proliferation activity than those within the central part of the epithelial mass (at 11 WD, labeling index: periphery 65% vs. center 15%, P < 0.001). In conclusion, the patterns of endocrine differentiation and epithelial proliferation observed within the human pancreas early in development suggest that the mesenchyme plays a role in these phenomena.
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M Polak , L Bouchareb-Banaei , R Scharfmann and P Czernichow Institut National de la Santé et de la Recherche Médicale (INSERM) U457, Department of Pediatric Endocrinology and Diabetes, Hôpital Robert Debré, Paris, France. michel.polak@rdb.ap-hop-paris.fr Abstract In the early human embryonic/fetal pancreas, we studied 1) the ontogenetic pattern of the endocrine cells and the evolution of the endocrine mass, and 2) the morphogenetic pattern of development and, more precisely, the complex relationship of the epithelial mass with the surrounding mesenchyme. We studied 15 pancreases between 7 and 11 weeks of development (WD) by double immunohistochemistry. Epithelial cells in these pancreatic anlage were detected by cytokeratin staining, and differentiated endocrine cells were detected by insulin, glucagon, somatostatin, and pancreatic polypeptide staining. Proliferation was quantified using a nuclear marker, the Ki-67 antibody. At this early stage, the pancreas is made up of an epithelial mass composed of central ducts intermingled with a loose mesenchyme and peripheral ducts surrounded by a dense peripancreatic mesenchyme. Hormone-containing cells appear in the epithelium at 8 WD. Newly differentiated endocrine cells coexpress insulin, glucagon, and somatostatin; endocrine differentiation starts within the central ducts of the epithelial mass, at a distance from the dense peripancreatic surrounding mesenchyme. The fraction of the primitive endocrine cells undergoing proliferation is low (5% of the insulin cells at 8 WD, 3% at 11 WD), which is in favor of massive differentiation as the major mechanism for increasing endocrine mass. By contrast, the nonendocrine epithelial cells have a higher rate of proliferation; the epithelial cells in contact with the dense peripancreatic surrounding mesenchyme show more proliferation activity than those within the central part of the epithelial mass (at 11 WD, labeling index: periphery 65% vs. center 15%, P &lt; 0.001). In conclusion, the patterns of endocrine differentiation and epithelial proliferation observed within the human pancreas early in development suggest that the mesenchyme plays a role in these phenomena.</description><identifier>ISSN: 0012-1797</identifier><identifier>EISSN: 1939-327X</identifier><identifier>DOI: 10.2337/diabetes.49.2.225</identifier><identifier>PMID: 10868939</identifier><identifier>CODEN: DIAEAZ</identifier><language>eng</language><publisher>Alexandria, VA: American Diabetes Association</publisher><subject>Analysis ; Biological and medical sciences ; Cell Division - physiology ; Development and progression ; Diabetes ; Diabetes mellitus ; Embryo, Mammalian - metabolism ; Embryo, Mammalian - physiology ; Embryonic and Fetal Development ; Endocrine manifestations ; Endocrine manifestations of general diseases ; Endocrine pancreas ; Epithelial Cells - cytology ; Fetal development ; Fetus ; Fundamental and applied biological sciences. Psychology ; Gestational Age ; Growth ; Humans ; Morphology. Functional localizations ; Pancreas ; Pancreas - cytology ; Pancreas - embryology ; Pancreatic Ducts - cytology ; Pancreatic Ducts - embryology ; Pancreatic Hormones - metabolism ; Physiological aspects ; Vertebrates: endocrinology</subject><ispartof>Diabetes (New York, N.Y.), 2000-02, Vol.49 (2), p.225-232</ispartof><rights>2000 INIST-CNRS</rights><rights>COPYRIGHT 2000 American Diabetes Association</rights><rights>COPYRIGHT 2000 American Diabetes Association</rights><rights>Copyright American Diabetes Association Feb 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c642t-f91730b4ddbac8e8c942f5f3c08ed7db2f2d1c75d56e69caa61f13d5b5e3782c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1363020$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10868939$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>POLAK, M</creatorcontrib><creatorcontrib>BOUCHAREB-BANAEI, L</creatorcontrib><creatorcontrib>SCHARFMANN, R</creatorcontrib><creatorcontrib>CZERNICHOW, P</creatorcontrib><title>Early pattern of differentiation in the human pancreas</title><title>Diabetes (New York, N.Y.)</title><addtitle>Diabetes</addtitle><description>Early pattern of differentiation in the human pancreas. M Polak , L Bouchareb-Banaei , R Scharfmann and P Czernichow Institut National de la Santé et de la Recherche Médicale (INSERM) U457, Department of Pediatric Endocrinology and Diabetes, Hôpital Robert Debré, Paris, France. michel.polak@rdb.ap-hop-paris.fr Abstract In the early human embryonic/fetal pancreas, we studied 1) the ontogenetic pattern of the endocrine cells and the evolution of the endocrine mass, and 2) the morphogenetic pattern of development and, more precisely, the complex relationship of the epithelial mass with the surrounding mesenchyme. We studied 15 pancreases between 7 and 11 weeks of development (WD) by double immunohistochemistry. Epithelial cells in these pancreatic anlage were detected by cytokeratin staining, and differentiated endocrine cells were detected by insulin, glucagon, somatostatin, and pancreatic polypeptide staining. Proliferation was quantified using a nuclear marker, the Ki-67 antibody. At this early stage, the pancreas is made up of an epithelial mass composed of central ducts intermingled with a loose mesenchyme and peripheral ducts surrounded by a dense peripancreatic mesenchyme. Hormone-containing cells appear in the epithelium at 8 WD. Newly differentiated endocrine cells coexpress insulin, glucagon, and somatostatin; endocrine differentiation starts within the central ducts of the epithelial mass, at a distance from the dense peripancreatic surrounding mesenchyme. The fraction of the primitive endocrine cells undergoing proliferation is low (5% of the insulin cells at 8 WD, 3% at 11 WD), which is in favor of massive differentiation as the major mechanism for increasing endocrine mass. By contrast, the nonendocrine epithelial cells have a higher rate of proliferation; the epithelial cells in contact with the dense peripancreatic surrounding mesenchyme show more proliferation activity than those within the central part of the epithelial mass (at 11 WD, labeling index: periphery 65% vs. center 15%, P &lt; 0.001). In conclusion, the patterns of endocrine differentiation and epithelial proliferation observed within the human pancreas early in development suggest that the mesenchyme plays a role in these phenomena.</description><subject>Analysis</subject><subject>Biological and medical sciences</subject><subject>Cell Division - physiology</subject><subject>Development and progression</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Embryo, Mammalian - metabolism</subject><subject>Embryo, Mammalian - physiology</subject><subject>Embryonic and Fetal Development</subject><subject>Endocrine manifestations</subject><subject>Endocrine manifestations of general diseases</subject><subject>Endocrine pancreas</subject><subject>Epithelial Cells - cytology</subject><subject>Fetal development</subject><subject>Fetus</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gestational Age</subject><subject>Growth</subject><subject>Humans</subject><subject>Morphology. 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M Polak , L Bouchareb-Banaei , R Scharfmann and P Czernichow Institut National de la Santé et de la Recherche Médicale (INSERM) U457, Department of Pediatric Endocrinology and Diabetes, Hôpital Robert Debré, Paris, France. michel.polak@rdb.ap-hop-paris.fr Abstract In the early human embryonic/fetal pancreas, we studied 1) the ontogenetic pattern of the endocrine cells and the evolution of the endocrine mass, and 2) the morphogenetic pattern of development and, more precisely, the complex relationship of the epithelial mass with the surrounding mesenchyme. We studied 15 pancreases between 7 and 11 weeks of development (WD) by double immunohistochemistry. Epithelial cells in these pancreatic anlage were detected by cytokeratin staining, and differentiated endocrine cells were detected by insulin, glucagon, somatostatin, and pancreatic polypeptide staining. Proliferation was quantified using a nuclear marker, the Ki-67 antibody. At this early stage, the pancreas is made up of an epithelial mass composed of central ducts intermingled with a loose mesenchyme and peripheral ducts surrounded by a dense peripancreatic mesenchyme. Hormone-containing cells appear in the epithelium at 8 WD. Newly differentiated endocrine cells coexpress insulin, glucagon, and somatostatin; endocrine differentiation starts within the central ducts of the epithelial mass, at a distance from the dense peripancreatic surrounding mesenchyme. The fraction of the primitive endocrine cells undergoing proliferation is low (5% of the insulin cells at 8 WD, 3% at 11 WD), which is in favor of massive differentiation as the major mechanism for increasing endocrine mass. By contrast, the nonendocrine epithelial cells have a higher rate of proliferation; the epithelial cells in contact with the dense peripancreatic surrounding mesenchyme show more proliferation activity than those within the central part of the epithelial mass (at 11 WD, labeling index: periphery 65% vs. center 15%, P &lt; 0.001). In conclusion, the patterns of endocrine differentiation and epithelial proliferation observed within the human pancreas early in development suggest that the mesenchyme plays a role in these phenomena.</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>10868939</pmid><doi>10.2337/diabetes.49.2.225</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Analysis
Biological and medical sciences
Cell Division - physiology
Development and progression
Diabetes
Diabetes mellitus
Embryo, Mammalian - metabolism
Embryo, Mammalian - physiology
Embryonic and Fetal Development
Endocrine manifestations
Endocrine manifestations of general diseases
Endocrine pancreas
Epithelial Cells - cytology
Fetal development
Fetus
Fundamental and applied biological sciences. Psychology
Gestational Age
Growth
Humans
Morphology. Functional localizations
Pancreas
Pancreas - cytology
Pancreas - embryology
Pancreatic Ducts - cytology
Pancreatic Ducts - embryology
Pancreatic Hormones - metabolism
Physiological aspects
Vertebrates: endocrinology
title Early pattern of differentiation in the human pancreas
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