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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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. |
doi_str_mv | 10.2337/diabetes.49.2.225 |
format | Article |
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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 < 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&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 < 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. Functional localizations</subject><subject>Pancreas</subject><subject>Pancreas - cytology</subject><subject>Pancreas - embryology</subject><subject>Pancreatic Ducts - cytology</subject><subject>Pancreatic Ducts - embryology</subject><subject>Pancreatic Hormones - metabolism</subject><subject>Physiological aspects</subject><subject>Vertebrates: endocrinology</subject><issn>0012-1797</issn><issn>1939-327X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpt0t2L1DAQAPAgird3-gf4IkXkELmu-Wja9PFYzlNYuBcF30KaTLo52nRNUvT-eyNdOVeXeQiE3-RjZhB6RfCaMtZ8ME51kCCuq3ZN15TyJ2hFWtaWjDbfnqIVxoSWpGmbM3Qe4z3GuM7xHJ0RLGqR4QrVNyoMD8VepQTBF5MtjLMWAvjkVHKTL5wv0g6K3Twqn53XAVR8gZ5ZNUR4eVgv0NePN182n8rt3e3nzfW21HVFU2lb0jDcVcZ0SgsQuq2o5ZZpLMA0pqOWGqIbbngNdauVqoklzPCOA2sE1ewCXS7n7sP0fYaY5OiihmFQHqY5yoZQwigRGb75B95Pc_D5bZKSusrfrXhGVwvq1QDSeTuloHQPHoIaJg_W5e1r3laCc1xlXp7gOQyMTp_y7458Jgl-pl7NMUpxuz2iV6eonoYBepC5hpu7I04WrsMUYwAr98GNKjxIguXvUZB_RkFWraQyj0LOeX2oyNyNYP7KWHqfwdsDUFGrwYbcWxcfHasZpjiz9wvbuX73wwV4vOv_S38BPwHKHw</recordid><startdate>20000201</startdate><enddate>20000201</enddate><creator>POLAK, M</creator><creator>BOUCHAREB-BANAEI, L</creator><creator>SCHARFMANN, R</creator><creator>CZERNICHOW, P</creator><general>American Diabetes Association</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8GL</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>20000201</creationdate><title>Early pattern of differentiation in the human pancreas</title><author>POLAK, M ; BOUCHAREB-BANAEI, L ; SCHARFMANN, R ; CZERNICHOW, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c642t-f91730b4ddbac8e8c942f5f3c08ed7db2f2d1c75d56e69caa61f13d5b5e3782c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Analysis</topic><topic>Biological and medical sciences</topic><topic>Cell Division - physiology</topic><topic>Development and progression</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Embryo, Mammalian - metabolism</topic><topic>Embryo, Mammalian - physiology</topic><topic>Embryonic and Fetal Development</topic><topic>Endocrine manifestations</topic><topic>Endocrine manifestations of general diseases</topic><topic>Endocrine pancreas</topic><topic>Epithelial Cells - cytology</topic><topic>Fetal development</topic><topic>Fetus</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gestational Age</topic><topic>Growth</topic><topic>Humans</topic><topic>Morphology. Functional localizations</topic><topic>Pancreas</topic><topic>Pancreas - cytology</topic><topic>Pancreas - embryology</topic><topic>Pancreatic Ducts - cytology</topic><topic>Pancreatic Ducts - embryology</topic><topic>Pancreatic Hormones - metabolism</topic><topic>Physiological aspects</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>POLAK, M</creatorcontrib><creatorcontrib>BOUCHAREB-BANAEI, L</creatorcontrib><creatorcontrib>SCHARFMANN, R</creatorcontrib><creatorcontrib>CZERNICHOW, P</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: High School</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetes (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>POLAK, M</au><au>BOUCHAREB-BANAEI, L</au><au>SCHARFMANN, R</au><au>CZERNICHOW, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early pattern of differentiation in the human pancreas</atitle><jtitle>Diabetes (New York, N.Y.)</jtitle><addtitle>Diabetes</addtitle><date>2000-02-01</date><risdate>2000</risdate><volume>49</volume><issue>2</issue><spage>225</spage><epage>232</epage><pages>225-232</pages><issn>0012-1797</issn><eissn>1939-327X</eissn><coden>DIAEAZ</coden><abstract>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.</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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issn | 0012-1797 1939-327X |
language | eng |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
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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