Induction of type Ⅱ alveolar epithelial cells apoptosis in mouse by lipopolysaccharide does not require TNF-α

被引:2
|
作者
宋勇
施毅
Alden H Harken
机构
[1] Department of Respiratory Medicine
[2] Jinling Hospital
[3] Nanjing University School of Medicine
[4] University of Colorado Health Sciences Center
[5] Denver Nanjing
[6] China
[7] Nanjing
[8] Colorado
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D O I
暂无
中图分类号
R363 [病理生理学];
学科分类号
摘要
To examine whether lipopolysaccharide (LPS)-induced apoptosis correlates with TNF-α release by type Ⅱ alveolar epithelial cells (AEC Ⅱ), whether TNF-α knockout (TNF KO) abrogates the induction of apoptosis by LPS and whether TNF-α is sufficient to induce apoptosis in this cell type Methods AEC Ⅱ were isolated from wild type mice and TNF KO mice Cells were stimulated with LPS or recombinant murine TNF-α for 24 h TNF-α in culture supernatant was determined by ELISA following LPS stimulation Apoptosis was determined by the terminal deoxynucleotidyl transferase end-labeling (TUNEL) assay after treatment with either LPS or TNF-α Results LPS induced apoptosis in wild type AEC Ⅱ in a concentration-dependent manner LPS-induced AEC Ⅱ apoptosis was accompanied by an 11-fold increase (from 0 073±0 065 ng/ml in control to 0 94±0 14 ng/ml in 50 μg/ml of LPS, P<0 01) in TNF-α release However, increasing concentrations (5 or 25 ng/ml) of recombinant murine TNF-α failed to induce AEC Ⅱ apoptosis In addition, apoptosis did occur in AEC Ⅱ isolated from TNF KO mice following LPS stimulation Conclusions This study confirms that LPS induces TNF-α release and apoptosis in murine AEC Ⅱ in vitro Exogenous TNF-α failed to induce AEC Ⅱ apoptosis, and apoptosis occurred following LPS stimulation in cells lacking the ability to produce TNF-α Taken together, these results suggest that LPS-induced AEC Ⅱ apoptosis occurs by a TNF-α-independent mechanism
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页数:5
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