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他汀类药物通过抑制Rac-Akt信号传导来抑制成骨细胞迁移。

Statins inhibit osteoblast migration by inhibiting Rac-Akt signaling.

作者信息

Fukuyama Ryo, Fujita Takashi, Azuma Yasutaka, Hirano Akihiko, Nakamuta Hiromichi, Koida Masao, Komori Toshihisa

机构信息

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan.

出版信息

Biochem Biophys Res Commun. 2004 Mar 12;315(3):636-42. doi: 10.1016/j.bbrc.2004.01.104.

Abstract

Cell migration is a key event in repair and remodeling of skeletal tissues, but the mechanism of osteoblast migration has not been resolved. Statins, which are inhibitors of 3-hydroxy-3-methylglutaryl CoA reductase, increase bone. However, the effect of statins on osteoblast migration remains to be clarified. We investigated the effect of fluvastatin and mevastatin on platelet-derived growth factor (PDGF)-induced migration of osteoblastic MC3T3-E1 cells. PDGF promoted osteoblast migration, while the statins inhibited PDGF-induced migration, and mevalonate and geranylgeranylpyrophosphate but not farnesylpyrophosphate abolished the effect of statins. Dominant-negative Rac severely inhibited PDGF-induced osteoblast migration and reduced Akt phosphorylation. Further, fluvastatin reduced Akt phosphorylation and dominant-negative Akt inhibited PDGF-induced osteoblast migration. These results demonstrate that statins inhibit PDGF-induced osteoblast migration and Rac-Akt signaling plays an important role in the osteoblast migration, and suggest that statins restrain Rac function by inhibiting geranylgeranylation of Rac, which leads to the reduction in Akt activation and osteoblast migration.

摘要

细胞迁移是骨骼组织修复和重塑过程中的关键事件,但成骨细胞迁移的机制尚未明确。他汀类药物是3-羟基-3-甲基戊二酰辅酶A还原酶的抑制剂,可促进骨生成。然而,他汀类药物对成骨细胞迁移的影响仍有待阐明。我们研究了氟伐他汀和美伐他汀对血小板衍生生长因子(PDGF)诱导的成骨细胞MC3T3-E1细胞迁移的影响。PDGF促进成骨细胞迁移,而他汀类药物抑制PDGF诱导的迁移,甲羟戊酸和香叶基香叶基焦磷酸而非法尼基焦磷酸可消除他汀类药物的作用。显性负性Rac严重抑制PDGF诱导的成骨细胞迁移并降低Akt磷酸化。此外,氟伐他汀降低Akt磷酸化,显性负性Akt抑制PDGF诱导的成骨细胞迁移。这些结果表明,他汀类药物抑制PDGF诱导的成骨细胞迁移,Rac-Akt信号通路在成骨细胞迁移中起重要作用,并提示他汀类药物通过抑制Rac的香叶基香叶基化来抑制Rac功能,从而导致Akt激活和成骨细胞迁移减少。

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