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一种人工合成肽通过钙调神经磷酸酶-TFEB 通路抑制自噬。

An artificial peptide inhibits autophagy through calcineurin-TFEB pathway.

机构信息

Department of Biochemistry and Molecular Biology, Gene Engineering and Biotechnology of Beijing Key Laboratory, College of Life Sciences, Beijing Normal University, Beijing 100875, China.

Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang 111016, China.

出版信息

Biochim Biophys Acta Mol Cell Res. 2024 Dec;1871(8):119853. doi: 10.1016/j.bbamcr.2024.119853. Epub 2024 Sep 30.

Abstract

We previously reported that a bioactive peptide (pep3) can potently inhibit the enzyme activity of purified calcineurin (CN). In this paper, we further demonstrate that transfected pep3 can strongly inhibit CN enzyme activity in HEK293 cells. Transcription factor EB (TFEB) plays an important role in the autophagy-lysosome pathway (ALP) as one of the substrates of CN, so we study the effect of pep3 on the CN-TFEB-ALP pathway. Pep3 can significantly inhibit the mRNA levels of the TFEB downstream genes and the expression of the autophagy-associated proteins, and autophagy flux in HEK293 cells. We also validated the inhibitory effect of pep3 on autophagy in mice. These findings may provide a new idea for discovering more CN inhibitors and autophagy inhibitory drugs.

摘要

我们之前报道过一种生物活性肽(pep3)可以强烈抑制纯化的钙调神经磷酸酶(CN)的酶活性。在本文中,我们进一步证明转染 pep3 可以强烈抑制 HEK293 细胞中的 CN 酶活性。转录因子 EB(TFEB)作为 CN 的底物之一,在自噬溶酶体途径(ALP)中发挥重要作用,因此我们研究了 pep3 对 CN-TFEB-ALP 途径的影响。pep3 可显著抑制 HEK293 细胞中 TFEB 下游基因的 mRNA 水平和自噬相关蛋白的表达,以及自噬流。我们还验证了 pep3 对小鼠自噬的抑制作用。这些发现可能为发现更多的 CN 抑制剂和自噬抑制剂药物提供了新的思路。

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