Hamet P, Hadrava V, Kruppa U, Tremblay J
Clinical Research Institute of Montreal, Quebec, Canada.
Hypertension. 1991 Jun;17(6 Pt 2):896-901. doi: 10.1161/01.hyp.17.6.896.
Previous studies demonstrated that in addition to an increased response to growth factors, cultured vascular smooth muscle cells derived from spontaneously hypertensive rats (SHRs) grow to a greater density than cells from normotensive Wistar-Kyoto (WKY) rats. Transforming growth factor beta 1 (TGF-beta 1) has a bimodal effect on vascular smooth muscle cell growth, depending on cell density. The present study investigated the relation between cell density and expression of the proto-oncogene c-fos and TGF-beta 1 in cells from WKY rats and SHRs. The results demonstrate an increased accumulation of c-fos mRNA in calf serum-stimulated SHR cells but only at a high cell density. The expression of TGF-beta 1 mRNA was enhanced in growing SHR cells at every density studied as early as 24 hours after inoculation, with a further increase at later times. The effect of exogenous TGF-beta 1 on new DNA synthesis was evaluated by [3H]thymidine incorporation. At a low cell density, TGF-beta 1 had no effect on DNA synthesis in either WKY or SHR vascular smooth muscle cells. At a high cell density, there was a significant increase of DNA synthesis in response to TGF-beta 1 in SHR cells without any effect in WKY cells. In conclusion, contact inhibition of vascular smooth muscle cells from SHRs at a higher cell density is accompanied by an earlier expression of the marker gene c-fos and preceded by an exaggerated expression of TGF-beta 1.(ABSTRACT TRUNCATED AT 250 WORDS)
先前的研究表明,除了对生长因子的反应增强外,源自自发性高血压大鼠(SHR)的培养血管平滑肌细胞比正常血压的Wistar-Kyoto(WKY)大鼠的细胞生长至更高的密度。转化生长因子β1(TGF-β1)对血管平滑肌细胞生长具有双峰效应,这取决于细胞密度。本研究调查了WKY大鼠和SHR大鼠细胞中细胞密度与原癌基因c-fos和TGF-β1表达之间的关系。结果表明,在小牛血清刺激的SHR细胞中,c-fos mRNA的积累增加,但仅在高细胞密度时出现。在接种后最早24小时,在每个研究密度下生长的SHR细胞中TGF-β1 mRNA的表达均增强,在随后的时间进一步增加。通过[3H]胸苷掺入评估外源性TGF-β1对新DNA合成的影响。在低细胞密度下,TGF-β1对WKY或SHR血管平滑肌细胞的DNA合成均无影响。在高细胞密度下,SHR细胞中对TGF-β1的反应导致DNA合成显著增加,而对WKY细胞则无影响。总之,SHR血管平滑肌细胞在较高细胞密度下的接触抑制伴随着标记基因c-fos的早期表达,并先于TGF-β1的过度表达。(摘要截短于250字)