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 |
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Zusammenfassung: | 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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ISSN: | 0012-1797 1939-327X |
DOI: | 10.2337/diabetes.49.2.225 |