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蛋白激酶C-α抑制肾细胞在S-(1,2-二氯乙烯基)-L-半胱氨酸损伤后氧化磷酸化的修复。

Protein kinase C-alpha inhibits the repair of oxidative phosphorylation after S-(1,2-dichlorovinyl)-L-cysteine injury in renal cells.

作者信息

Liu Xiuli, Godwin Malinda L, Nowak Grazyna

机构信息

Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.

出版信息

Am J Physiol Renal Physiol. 2004 Jul;287(1):F64-73. doi: 10.1152/ajprenal.00216.2003. Epub 2004 Mar 2.

Abstract

Previously, we showed that physiological functions of renal proximal tubular cells (RPTC) do not recover following S-(1,2-dichlorovinyl)-l-cysteine (DCVC)-induced injury. This study investigated the role of protein kinase C-alpha (PKC-alpha) in the lack of repair of mitochondrial function in DCVC-injured RPTC. After DCVC exposure, basal oxygen consumption (Qo(2)), uncoupled Qo(2), oligomycin-sensitive Qo(2), F(1)F(0)-ATPase activity, and ATP production decreased, respectively, to 59, 27, 27, 57, and 68% of controls. None of these functions recovered. Mitochondrial transmembrane potential decreased 53% after DCVC injury but recovered on day 4. PKC-alpha was activated 4.3- and 2.5-fold on days 2 and 4, respectively, of the recovery period. Inhibition of PKC-alpha activation (10 nM Go6976) did not block DCVC-induced decreases in mitochondrial functions but promoted the recovery of uncoupled Qo(2), oligomycin-sensitive Qo(2), F(1)F(0)-ATPase activity, and ATP production. Protein levels of the catalytic beta-subunit of F(1)F(0)-ATPase were not changed by DCVC or during the recovery period. Amino acid sequence analysis revealed that alpha-, beta-, and epsilon-subunits of F(1)F(0)-ATPase have PKC consensus motifs. Recombinant PKC-alpha phosphorylated the beta-subunit and decreased F(1)F(0)-ATPase activity in vitro. Serine but not threonine phosphorylation of the beta-subunit was increased during late recovery following DCVC injury, and inhibition of PKC-alpha activation decreased this phosphorylation. We conclude that during RPTC recovery following DCVC injury, 1). PKC-alpha activation decreases F(0)F(1)-ATPase activity, oxidative phosphorylation, and ATP production; 2). PKC-alpha phosphorylates the beta-subunit of F(1)F(0)-ATPase on serine residue; and 3). PKC-alpha does not mediate depolarization of RPTC mitochondria. This is the first report showing that PKC-alpha phosphorylates the catalytic subunit of F(1)F(0)-ATPase and that PKC-alpha plays an important role in regulating repair of mitochondrial function.

摘要

此前,我们发现肾近端小管细胞(RPTC)在受到S-(1,2-二氯乙烯基)-L-半胱氨酸(DCVC)诱导的损伤后,其生理功能无法恢复。本研究调查了蛋白激酶C-α(PKC-α)在DCVC损伤的RPTC线粒体功能修复缺失中的作用。DCVC暴露后,基础氧消耗(Qo₂)、解偶联Qo₂、寡霉素敏感Qo₂、F₁F₀-ATP酶活性和ATP生成分别降至对照值的59%、27%、27%、57%和68%。这些功能均未恢复。DCVC损伤后线粒体跨膜电位下降53%,但在第4天恢复。在恢复期的第2天和第4天,PKC-α分别被激活4.3倍和2.5倍。抑制PKC-α激活(10 nM Go6976)并未阻止DCVC诱导的线粒体功能下降,但促进了解偶联Qo₂、寡霉素敏感Qo₂、F₁F₀-ATP酶活性和ATP生成的恢复。F₁F₀-ATP酶催化β亚基的蛋白水平在DCVC处理后或恢复期未发生变化。氨基酸序列分析显示,F₁F₀-ATP酶的α、β和ε亚基具有PKC共有基序。重组PKC-α在体外使β亚基磷酸化并降低F₁F₀-ATP酶活性。DCVC损伤后恢复期晚期,β亚基的丝氨酸而非苏氨酸磷酸化增加,抑制PKC-α激活可减少这种磷酸化。我们得出结论,在DCVC损伤后的RPTC恢复过程中,1). PKC-α激活降低F₀F₁-ATP酶活性、氧化磷酸化和ATP生成;2). PKC-α使F₁F₀-ATP酶的β亚基在丝氨酸残基上磷酸化;3). PKC-α不介导RPTC线粒体的去极化。这是首次报道PKC-α使F₁F₀-ATP酶催化亚基磷酸化,且PKC-α在调节线粒体功能修复中起重要作用。

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