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血小板衍生生长因子样分子的发育调控产生

Developmentally regulated production of platelet-derived growth factor-like molecules.

作者信息

Seifert R A, Schwartz S M, Bowen-Pope D F

出版信息

Nature. 1984;311(5987):669-71. doi: 10.1038/311669a0.

Abstract

Platelet-derived growth factor (PDGF) is thought to mediate the proliferation of smooth muscle cells in injured arteries, and may be involved in the pathogenesis of atherosclerosis. PDGF-like molecules from non-platelet sources may also play a role in the regulation of cell activity in other circumstances. Transformation of cells by a wide range of oncongenic agents appears to activate a cellular gene encoding a PDGF-like molecule, possibly accounting for the ability of transformed cells to grow without addition of exogenous mitogens. We show here that a molecule (PDGF-c) which can compete with 125I-PDGF for binding to PDGF receptors is secreted by cultured rat aortic smooth muscle cells (rASMC) isolated from 13 to 18-day-old rats (pups) but not from three-month-old animals (adults). Thus, production of PDGF-c appears to be developmentally regulated and may be a factor in the more rapid proliferation of rASMC and synthesis of connective tissue components which occurs during growth of the aorta in vivo.

摘要

血小板衍生生长因子(PDGF)被认为可介导受损动脉中平滑肌细胞的增殖,并可能参与动脉粥样硬化的发病机制。来自非血小板来源的PDGF样分子在其他情况下也可能在细胞活性调节中发挥作用。多种致癌剂使细胞发生转化似乎会激活一个编码PDGF样分子的细胞基因,这可能解释了转化细胞在不添加外源性有丝分裂原的情况下仍能生长的能力。我们在此表明,一种能与125I-PDGF竞争结合PDGF受体的分子(PDGF-c)是由从13至18日龄大鼠(幼崽)分离的培养大鼠主动脉平滑肌细胞(rASMC)分泌的,而从三月龄动物(成年动物)分离的细胞则不分泌。因此,PDGF-c的产生似乎受发育调控,并且可能是体内主动脉生长过程中rASMC更快增殖和结缔组织成分合成的一个因素。

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