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Division of Nephrology and Hypertension, Northwestern University Medical School, Chicago, Illinois 60611
The effect of hypoxia
on the proliferation and collagen synthesis of cultured rat mesangial
cells was examined under normal-glucose (NG, 5 mM) and high-glucose
(HG, 25 mM)-media conditions. In addition, a role for osteopontin (OPN)
in mediating these processes was assessed. Quiescent cultures were
exposed to hypoxia (3% O2) and normoxia (18%
O2) in a serum-free medium with NG or HG, and cell proliferation, collagen synthesis, and OPN expression were assessed. Cells exposed to hypoxia in NG medium resulted in significant increases
in [3H]thymidine incorporation, cell number, and
[3H]proline incorporation, respectively. HG incubations
also produced significant stimulation of these parameters under
normoxic conditions, which were markedly enhanced in cells exposed to
hypoxia in HG medium. In addition, hypoxia and HG stimulated the mRNA
levels of type IV collagen, and the combination of hypoxia and HG
resulted in additive increases in type IV collagen expression. Hypoxia and HG also stimulated OPN mRNA and protein levels in an additive fashion. A neutralizing antibody to OPN or its
3-integrin receptor significantly blocked the effect of
hypoxia and HG on proliferation and collagen synthesis. In conclusion,
these results demonstrate for the first time that hypoxia in HG medium
produces exaggerated mesangial cell growth and type IV collagen
synthesis. In addition, OPN appears to play a role in mediating the
accelerated mesangial cell growth and collagen synthesis found in a
hyperglycemic and hypoxic environment.
chronic hypoxia; hyperglycemia; mesangial cells; cell proliferation; extracellular matrix; diabetes
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