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Diabetes, Vol 47, Issue 1 134-137, Copyright © 1998 by American Diabetes Association
Culture of adult human islet preparations with hepatocyte growth factor and 804G matrix is mitogenic for duct cells but not for beta-cells
VH Lefebvre, T Otonkoski, J Ustinov, MA Huotari, DG Pipeleers and L Bouwens
Diabetes Research Center, Vrije Universiteit Brussel, Brussels, Belgium. velefeb@mebo.vub.ac.be
It has recently been reported that human adult beta-cells proliferate
during culture on an extracellular matrix prepared from rat 804G cells and
in the presence of hepatocyte growth factor (HGF). The present study
compares the mitogenic effect of this condition on human beta-cells and on
neighboring non-endocrine duct cells. Islet cell-enriched fractions were
prepared from adult human organ donors and cultured in suspension or on
804G matrix, with or without HGF. The combination of 804G matrix and HGF
increased the number of 5-bromo-2'-deoxyuridine-positive (BrdU+) cells
within 48 h reaching a maximum after 4 days. In sections, virtually all
BrdU+ cells were negative for insulin or glucagon and for preproinsulin
mRNA but expressed the ductal cell markers cytokeratin 19 and 7, carbonic
anhydrase-II, and carbohydrate antigen 19-9. After 4 days of culture, the
cytokeratin 19+ ductal cells exhibited a BrdU-labeling index of 30% (P <
0.01 vs. 2% without HGF and matrix), whereas <0.1% of insulin-positive
and <1% of glucagon-positive cells were labeled. Formation of bilayers
with ductal cells covering the endocrine cells may cause erroneous
interpretation on double positivity in unsectioned tissue. It is concluded
that culture of human islet cell preparations with HGF and 804G matrix
stimulates the proliferation of the duct cells but not of the underlying
beta-cells.

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Copyright © 1998 by the American Diabetes Association.
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