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Diabetes, Vol 39, Issue 4 401-405, Copyright © 1990 by American Diabetes Association
Islet mass and function in diabetes and transplantation
GC Weir, S Bonner-Weir and JL Leahy
Joslin Diabetes Center, New England Deaconess Hospital, Boston, MA 02215.
The concept of pancreatic beta-cell mass is fundamental to the
understanding of normal metabolism, the pathogenesis of diabetes, and the
transplantation of beta-cell tissue. The amount of beta-cell tissue present
in the pancreas is a major determinant of the quantity of insulin that can
be secreted, and its mass will vary according to the size of the individual
and the degree of insulin resistance present. Not all insulin-producing
cells are the same, and the dimensions of this heterogeneity remain to be
defined. Pancreatic beta-cell mass is markedly reduced in insulin-dependent
diabetes mellitus and moderately reduced in non-insulin-dependent diabetes
mellitus. In both forms of diabetes, there are qualitative and quantitative
abnormalities of insulin secretion that cannot be explained entirely by
changes in beta-cell mass. The amount of beta-cell tissue needed for
successful transplantation has only been partially defined. Segmental
(approximately 50% of the pancreas) transplantation can normalize plasma
glucose levels in humans. Difficulty obtaining sufficient amounts of
beta-cell tissue is expected to remain a barrier to successful islet
transplantation for the immediate future. More should be learned about the
function and fate of grafted islet cells.

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Copyright © 1990 by the American Diabetes Association.
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