The midgestational human fetal pancreas contains cells coexpressing islet hormones
- PMID: 1356859
- DOI: 10.1016/0012-1606(92)90121-v
The midgestational human fetal pancreas contains cells coexpressing islet hormones
Abstract
In the fetal development of the mouse pancreas, endocrine cells have been found that express more than one hormone simultaneously. Our objective was to evaluate the existence of such cells in the human fetal pancreas. We found cells coexpressing two of the major pancreatic hormones (insulin, glucagon, and somatostatin) in sections of eight midgestational (12-18 weeks) pancreata and in 0-7% of cells in single-cell suspensions from midgestational pancreata. By electron microscopy, using granule morphology and immunoelectron microscopic techniques, we could confirm these findings and even detect cells containing three hormones. Morphologically different granules contained different immunoreactivities, suggesting parallel regulation of hormone production and packaging. In six newborn pancreata (born after 22-40 weeks of gestation), we could not find any multiple-hormone-containing cells. Subsequently, we evaluated whether multiple-hormone-containing cells proliferate by using pancreatic fragments and single-cell preparations at the light and electron microscopic level (six pancreata). No endocrine hormone-containing cells incorporated bromodeoxyuridine during a 1-hr culture period, indicating that these cells have lost the ability to proliferate under the conditions chosen. We conclude that, as in mice, the human fetal pancreas of 12-18 weeks of gestation contains endocrine cells that express multiple hormones simultaneously. These (multiple) hormone-containing cells do not seem to proliferate under basal conditions.
Similar articles
-
Ultrastructural studies of the ontogeny of fetal human and porcine endocrine pancreas, with special reference to colocalization of the four major islet hormones.Dev Biol. 1992 Oct;153(2):376-85. doi: 10.1016/0012-1606(92)90122-w. Dev Biol. 1992. PMID: 1356860
-
The transplanted fetal endocrine pancreas undergoes an inherent sequential differentiation similar to that in the native pancreas. An ultrastructural study in the pig-to-mouse model.Diabetes. 2001 May;50(5):962-71. doi: 10.2337/diabetes.50.5.962. Diabetes. 2001. PMID: 11334439
-
Cellular distribution of insulin, glucagon, pancreatic polypeptide hormone and somatostatin in the fetal and adult pancreas of the guinea pig: a comparative immunohistochemical study.Eur J Cell Biol. 1985 Sep;38(2):301-5. Eur J Cell Biol. 1985. PMID: 2864246
-
Four hormones in the pancreas of the lizard, Anolis carolinensis.Anat Rec. 1981 Jan;199(1):89-97. doi: 10.1002/ar.1091990109. Anat Rec. 1981. PMID: 6111934
-
Ontogeny of endocrine cells in porcine gut and pancreas. An immunocytochemical study.Gastroenterology. 1983 Dec;85(6):1359-72. Gastroenterology. 1983. PMID: 6138293 Review.
Cited by
-
Enhanced differentiation of human amniotic fluid-derived stem cells into insulin-producing cells in vitro.J Diabetes Investig. 2017 Jan;8(1):34-43. doi: 10.1111/jdi.12544. Epub 2016 Jun 30. J Diabetes Investig. 2017. PMID: 27240324 Free PMC article.
-
Comparative and integrative single cell analysis reveals new insights into the transcriptional immaturity of stem cell-derived β cells.BMC Genomics. 2024 Jan 24;25(1):105. doi: 10.1186/s12864-024-10013-x. BMC Genomics. 2024. PMID: 38267908 Free PMC article.
-
Zebrafish mnx1 controls cell fate choice in the developing endocrine pancreas.Development. 2011 Nov;138(21):4597-608. doi: 10.1242/dev.067736. Development. 2011. PMID: 21989909 Free PMC article.
-
Differentiated human stem cells resemble fetal, not adult, β cells.Proc Natl Acad Sci U S A. 2014 Feb 25;111(8):3038-43. doi: 10.1073/pnas.1400709111. Epub 2014 Feb 10. Proc Natl Acad Sci U S A. 2014. PMID: 24516164 Free PMC article.
-
Mouse muscle as an ectopic permissive site for human pancreatic development.Diabetes. 2013 Oct;62(10):3479-87. doi: 10.2337/db13-0554. Epub 2013 Jul 8. Diabetes. 2013. PMID: 23835344 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
