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PKM2 在足细胞中的特异性缺失通过β-连环蛋白减轻 LPS 诱导的足细胞损伤。

Podocyte specific deletion of PKM2 ameliorates LPS-induced podocyte injury through beta-catenin.

机构信息

Department of Nutrition, The University of Tennessee Knoxville, 1215 Cumberland Avenue, 229 Jessie Harris Building, Knoxville, TN, 37996-0840, USA.

Department of Community Health Sciences, King Saud University, Riyadh, Saudi Arabia.

出版信息

Cell Commun Signal. 2022 May 30;20(1):76. doi: 10.1186/s12964-022-00884-6.

Abstract

BACKGROUND

Acute kidney injury (AKI) is associated with a severe decline in kidney function caused by abnormalities within the podocytes' glomerular matrix. Recently, AKI has been linked to alterations in glycolysis and the activity of glycolytic enzymes, including pyruvate kinase M2 (PKM2). However, the contribution of this enzyme to AKI remains largely unexplored.

METHODS

Cre-loxP technology was used to examine the effects of PKM2 specific deletion in podocytes on the activation status of key signaling pathways involved in the pathophysiology of AKI by lipopolysaccharides (LPS). In addition, we used lentiviral shRNA to generate murine podocytes deficient in PKM2 and investigated the molecular mechanisms mediating PKM2 actions in vitro.

RESULTS

Specific PKM2 deletion in podocytes ameliorated LPS-induced protein excretion and alleviated LPS-induced alterations in blood urea nitrogen and serum albumin levels. In addition, PKM2 deletion in podocytes alleviated LPS-induced structural and morphological alterations to the tubules and to the brush borders. At the molecular level, PKM2 deficiency in podocytes suppressed LPS-induced inflammation and apoptosis. In vitro, PKM2 knockdown in murine podocytes diminished LPS-induced apoptosis. These effects were concomitant with a reduction in LPS-induced activation of β-catenin and the loss of Wilms' Tumor 1 (WT1) and nephrin. Notably, the overexpression of a constitutively active mutant of β-catenin abolished the protective effect of PKM2 knockdown. Conversely, PKM2 knockdown cells reconstituted with the phosphotyrosine binding-deficient PKM2 mutant (K433E) recapitulated the effect of PKM2 depletion on LPS-induced apoptosis, β-catenin activation, and reduction in WT1 expression.

CONCLUSIONS

Taken together, our data demonstrates that PKM2 plays a key role in podocyte injury and suggests that targetting PKM2 in podocytes could serve as a promising therapeutic strategy for AKI.

TRIAL REGISTRATION

Not applicable. Video abstract.

摘要

背景

急性肾损伤 (AKI) 与肾小球基质中足细胞的异常导致的肾功能严重下降有关。最近,AKI 与糖酵解和糖酵解酶(包括丙酮酸激酶 M2 (PKM2))的活性改变有关。然而,该酶对 AKI 的贡献在很大程度上仍未得到探索。

方法

使用 Cre-loxP 技术研究通过脂多糖 (LPS) 特异性删除足细胞中的 PKM2 对参与 AKI 病理生理学的关键信号通路的激活状态的影响。此外,我们使用慢病毒 shRNA 生成缺乏 PKM2 的鼠足细胞,并在体外研究介导 PKM2 作用的分子机制。

结果

特异性删除足细胞中的 PKM2 可改善 LPS 诱导的蛋白质排泄,并减轻 LPS 诱导的血尿素氮和血清白蛋白水平的改变。此外,足细胞中 PKM2 的缺失减轻了 LPS 诱导的肾小管和刷状缘的结构和形态改变。在分子水平上,足细胞中 PKM2 的缺失抑制了 LPS 诱导的炎症和细胞凋亡。在体外,鼠足细胞中 PKM2 的敲低减少了 LPS 诱导的细胞凋亡。这些作用与 LPS 诱导的 β-连环蛋白激活和 Wilms' Tumor 1 (WT1) 和足细胞蛋白的丢失减少有关。值得注意的是,过表达组成型活性突变的 β-连环蛋白消除了 PKM2 敲低的保护作用。相反,用磷酸酪氨酸结合缺陷的 PKM2 突变体 (K433E) 重建的 PKM2 敲低细胞再现了 PKM2 缺失对 LPS 诱导的细胞凋亡、β-连环蛋白激活和 WT1 表达减少的影响。

结论

综上所述,我们的数据表明 PKM2 在足细胞损伤中起关键作用,并表明靶向足细胞中的 PKM2 可能是 AKI 的一种有前途的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/9150347/d78e600cbda2/12964_2022_884_Fig1_HTML.jpg

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