Green R S, Lieb M E, Weintraub A S, Gacheru S N, Rosenfield C L, Shah S, Kagan H M, Taubman M B
Department of Pediatrics, Mt. Sinai School of Medicine, New York, New York, USA.
Lab Invest. 1995 Oct;73(4):476-82.
Atherosclerosis and arterial injury are characterized by vascular smooth muscle cell (VSMC) migration and growth and an increase in synthesis of extracellular matrix. Platelet-derived growth factor (PDGF) has been implicated in these processes. This study was designed to identify additional PDGF-regulated genes in VSMC.
A cDNA library prepared from PDGF-stimulated rat aortic VSMC was screened by differential hybridization to identify clones representing PDGF-inducible genes. The time course of growth factor-induced changes in gene expression was examined by RNA blot hybridization. Assays of protein activity were also performed for selected gene products.
Four PDGF-regulated cDNA clones were identified by DNA sequencing. These encoded the extracellular matrix proteins lysyl oxidase (LO), thrombospondin, and osteopontin and the intracellular enzyme lactate dehydrogenase (LDH). Levels of mRNA corresponding to all four genes were low in quiescent VSMC and were markedly induced by PDGF, angiotensin II, and 10% calf serum. The regulation of LO and LDH mRNA by these agonists in VSMC has not been previously reported. LO enzymatic activity in the culture media was increased by approximately equals to 700% after exposure to PDGF. In contrast, LDH activity was not increased by PDGF treatment.
The induction of LO mRNA and its secretion by VSMC is an early event accompanying growth factor stimulation and may contribute to organization of the extracellular matrix.
动脉粥样硬化和动脉损伤的特征是血管平滑肌细胞(VSMC)迁移、生长以及细胞外基质合成增加。血小板衍生生长因子(PDGF)与这些过程有关。本研究旨在鉴定VSMC中其他受PDGF调控的基因。
通过差异杂交筛选由PDGF刺激的大鼠主动脉VSMC制备的cDNA文库,以鉴定代表PDGF诱导基因的克隆。通过RNA印迹杂交检测生长因子诱导的基因表达变化的时间进程。还对选定的基因产物进行了蛋白质活性测定。
通过DNA测序鉴定出四个受PDGF调控的cDNA克隆。这些克隆编码细胞外基质蛋白赖氨酰氧化酶(LO)、血小板反应蛋白和骨桥蛋白以及细胞内酶乳酸脱氢酶(LDH)。在静止的VSMC中,对应于所有四个基因的mRNA水平较低,并且被PDGF、血管紧张素II和10%小牛血清显著诱导。这些激动剂对VSMC中LO和LDH mRNA的调控此前未见报道。暴露于PDGF后,培养基中的LO酶活性增加了约700%。相反,PDGF处理未增加LDH活性。
VSMC诱导LO mRNA及其分泌是生长因子刺激后的早期事件,可能有助于细胞外基质的组织。