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血小板衍生生长因子诱导的磷脂酶C激活并非DNA合成诱导所必需。

PDGF-induced activation of phospholipase C is not required for induction of DNA synthesis.

作者信息

Hill T D, Dean N M, Mordan L J, Lau A F, Kanemitsu M Y, Boynton A L

机构信息

Cancer Research Center of Hawaii, University of Hawaii, Honolulu 96813.

出版信息

Science. 1990 Jun 29;248(4963):1660-3. doi: 10.1126/science.2163545.

Abstract

Platelet-derived growth factor (PDGF) induction of DNA synthesis is believed to involve activation of phospholipase C (PLC) and subsequent accumulation of inositol 1,4,5-triphosphate [I(1,4,5)P3], increase in intracellular Ca2+, activation of protein kinase C (PKC), and receptor down regulation. Generation of these events is triggered by the tyrosine protein kinase (TPK) activity of the PDGF receptor. The TPK inhibitor genistein blocked PDGF induction of these events, including DNA synthesis, with the exception of receptor down regulation. PDGF-induced phosphotyrosine phosphorylations, including receptor autophosphorylation, were inhibited by genistein. Removal of genistein and PDGF resulted in DNA synthesis without the occurrence of PLC activation. These findings indicate that these early events, with the exception of receptor down regulation, are not necessary for PDGF-induced DNA synthesis.

摘要

血小板衍生生长因子(PDGF)诱导的DNA合成被认为涉及磷脂酶C(PLC)的激活以及随后肌醇1,4,5-三磷酸[I(1,4,5)P3]的积累、细胞内Ca2+增加、蛋白激酶C(PKC)激活和受体下调。这些事件的产生是由PDGF受体的酪氨酸蛋白激酶(TPK)活性触发的。TPK抑制剂染料木黄酮阻断了PDGF对这些事件的诱导,包括DNA合成,但受体下调除外。染料木黄酮抑制了PDGF诱导的磷酸酪氨酸磷酸化,包括受体自身磷酸化。去除染料木黄酮和PDGF后,DNA合成发生,而未出现PLC激活。这些发现表明,除受体下调外,这些早期事件对于PDGF诱导的DNA合成并非必需。

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