AI Article Synopsis

  • The study involved culturing smooth muscle cells from rat mesenteric arterioles using a novel technique that combines iron oxide injection and collagenase digestion.
  • Researchers confirmed the high purity of the smooth muscle cells used in their experiments (over 98%) through various methods like morphology and specific staining.
  • Findings revealed that growth factors like platelet-derived growth factor and angiotensin II promote cell proliferation, while nitric oxide can inhibit this growth, suggesting a complex interaction in the regulation of smooth muscle cell growth.

Article Abstract

We cultured smooth muscle cells as explants from rat mesenteric arterioles (40-200 microns in diameter) obtained by injecting a suspension of iron oxide intraarterially and magnetically separating the arterioles after collagenase digestion of adventitial tissue. In third-passaged cells we ascertained smooth muscle purity of > 98% by characteristic morphology, contraction responses, and specific immunofluorescence staining. Treatment of growth-arrested (in 0.4% fetal calf serum) cells with platelet-derived growth factor (0.3-7.5 nM) or angiotensin II (0.001-1000 nM) induced 3H-thymidine incorporation and cell proliferation in a dose-dependent manner (P < 0.01). S-nitroso-N acetylpenicillamine (0.05-0.5 mM), a nitric oxide-generating compound, inhibited 10% fetal calf serum-induced 3H-thymidine incorporation (P < 0.05) and cell proliferation (P < 0.01). The antimitogenic effect of S-nitroso-N-acetylpenicillamine was significantly reduced by hemoglobin and potentiated by superoxide dismutase (P < 0.01). In addition to a new technique for culturing mesenteric arteriolar smooth muscle cells, these findings provide evidence that platelet-derived growth factor, angiotensin II, and nitric oxide may be involved in their growth control.

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http://dx.doi.org/10.1007/BF00305381DOI Listing

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