Recombinant Klotho protein protects pulmonary alveolar epithelial cells against sepsis-induced apoptosis by inhibiting the Bcl-2/Bax/caspase-3 pathway.

IF 2.1 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Xiao Bo Li, Jia Li Liu, Shuang Zhao, Jing Li, Guang-Yan Zhang, Qing Tang, Wei Yong Chen
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引用次数: 0

Abstract

Background: Inflammation-induced apoptosis of alveolar type II epithelial cells is a primary contributor to sepsis-induced acute respiratory distress syndrome (ARDS). Klotho is a single-pass transmembrane protein with anti-inflammatory and anti-apoptotic effects. However, the role and mechanism of Klotho in the development of ARDS remains unknown.

Objectives: This study aimed to investigate the effect of Klotho on sepsis-induced apoptosis in human pulmonary alveolar epithelial cells (HPAEpiCs) together with the potential mechanism.

Material and methods: Cecal ligation and puncture (CLP) were performed to generate an in vivo sepsis model, and HPAEpiCs were treated with lipopolysaccharide (LPS) to mimic sepsis in vitro. Both models were administered recombinant Klotho protein. The morphology of the lung tissue was observed, and apoptotic cells and cell viability were detected. Interleukin (IL)-1β, IL-6, and tumor necrosis factor alpha (TNF-α) levels were detected using enzyme-linked immunosorbent assay (ELISA), while the expression of Bcl-2, Bax and cleaved caspase-3 was detected with western blotting.

Results: Klotho reversed the CLP-induced decrease in mouse survival in vivo (p < 0.001) and increased inflammatory cell infiltration and inflammatory substance exudation in the lung tissue of mice with sepsis (both p < 0.001). Klotho also suppressed apoptosis (p < 0.001) as demonstrated by IL-1β, IL-6 and TNF-α expression (all p < 0.001), and Bcl-2/Bax/caspase-3 pathway activation (p < 0.001). Klotho pretreatment significantly prevented LPS-induced apoptosis in vitro (p < 0.001), as demonstrated by IL-1β, IL-6 and TNF-α upregulation (all p < 0.001); and Bcl-2/Bax/caspase-3 pathway activation in HPAEpiCs (p < 0.001).

Conclusions: This study demonstrated that Klotho can ameliorate acute lung injury (ALI) induced by sepsis by inhibiting inflammatory responses and exerting anti-apoptotic effects by suppressing Bcl-2/Bax/caspase-3 pathway activation.

重组 Klotho 蛋白通过抑制 Bcl-2/Bax/caspase-3 通路,保护肺泡上皮细胞免受败血症诱导的细胞凋亡。
背景:炎症诱导的肺泡 II 型上皮细胞凋亡是败血症诱发急性呼吸窘迫综合征(ARDS)的主要原因。Klotho 是一种单通道跨膜蛋白,具有抗炎和抗凋亡作用。然而,Klotho在ARDS发病中的作用和机制仍不清楚:本研究旨在探讨 Klotho 对脓毒症诱导的人肺泡上皮细胞(HPAEpiCs)凋亡的影响及其潜在机制:材料和方法:采用盲肠结扎术(CLP)产生体内败血症模型,并用脂多糖(LPS)处理人肺泡上皮细胞(HPAEpiCs)以模拟体外败血症。两种模型都服用了重组 Klotho 蛋白。观察肺组织的形态,检测凋亡细胞和细胞活力。用酶联免疫吸附试验(ELISA)检测白细胞介素(IL)-1β、IL-6和肿瘤坏死因子α(TNF-α)的水平,用Western印迹法检测Bcl-2、Bax和裂解的caspase-3的表达:结果:Klotho逆转了CLP诱导的小鼠体内存活率下降(p < 0.001),并增加了败血症小鼠肺组织中的炎性细胞浸润和炎性物质渗出(p均 < 0.001)。Klotho还能抑制细胞凋亡(p < 0.001),表现为IL-1β、IL-6和TNF-α的表达(均p < 0.001),以及Bcl-2/Bax/caspase-3通路的激活(p < 0.001)。Klotho预处理可明显预防LPS诱导的体外细胞凋亡(p < 0.001),表现为IL-1β、IL-6和TNF-α的上调(均p < 0.001);以及HPAEpiCs中Bcl-2/Bax/caspase-3通路的激活(p < 0.001):本研究表明,Klotho能抑制炎症反应,并通过抑制Bcl-2/Bax/caspase-3通路的激活发挥抗凋亡作用,从而改善脓毒症诱发的急性肺损伤(ALI)。
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来源期刊
Advances in Clinical and Experimental Medicine
Advances in Clinical and Experimental Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.70
自引率
4.80%
发文量
153
审稿时长
6-12 weeks
期刊介绍: Advances in Clinical and Experimental Medicine has been published by the Wroclaw Medical University since 1992. Establishing the medical journal was the idea of Prof. Bogumił Halawa, Chair of the Department of Cardiology, and was fully supported by the Rector of Wroclaw Medical University, Prof. Zbigniew Knapik. Prof. Halawa was also the first editor-in-chief, between 1992-1997. The journal, then entitled "Postępy Medycyny Klinicznej i Doświadczalnej", appeared quarterly. Prof. Leszek Paradowski was editor-in-chief from 1997-1999. In 1998 he initiated alterations in the profile and cover design of the journal which were accepted by the Editorial Board. The title was changed to Advances in Clinical and Experimental Medicine. Articles in English were welcomed. A number of outstanding representatives of medical science from Poland and abroad were invited to participate in the newly established International Editorial Staff. Prof. Antonina Harłozińska-Szmyrka was editor-in-chief in years 2000-2005, in years 2006-2007 once again prof. Leszek Paradowski and prof. Maria Podolak-Dawidziak was editor-in-chief in years 2008-2016. Since 2017 the editor-in chief is prof. Maciej Bagłaj. Since July 2005, original papers have been published only in English. Case reports are no longer accepted. The manuscripts are reviewed by two independent reviewers and a statistical reviewer, and English texts are proofread by a native speaker. The journal has been indexed in several databases: Scopus, Ulrich’sTM International Periodicals Directory, Index Copernicus and since 2007 in Thomson Reuters databases: Science Citation Index Expanded i Journal Citation Reports/Science Edition. In 2010 the journal obtained Impact Factor which is now 1.179 pts. Articles published in the journal are worth 15 points among Polish journals according to the Polish Committee for Scientific Research and 169.43 points according to the Index Copernicus. Since November 7, 2012, Advances in Clinical and Experimental Medicine has been indexed and included in National Library of Medicine’s MEDLINE database. English abstracts printed in the journal are included and searchable using PubMed http://www.ncbi.nlm.nih.gov/pubmed.
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