Abstract | BACKGROUND: METHODS: Indirect immunofluorescence assay was used to detect SP-A distribution and expression in HK-2 cells. HK-2 cells were treated with various concentrations of LPS (0, 0.1, 1, 2, 5, and 10 mg/L) for 8 hours and with 5 mg/L LPS for different times (0, 2, 4, 8, 16, and 24 hours) to determine the effects of LPS on SP-A and TNF-α expression. Then, HK-2 cells were transfected with SP-A siRNA to analyze nuclear factor κB (NF-κB) P65 and TNF-α expression of HK-2 cells after LPS-treatment. RESULTS: Indirect immunofluorescence assay revealed that SP-A is localized to the membrane and cytoplasm of HK-2 cells. Interestingly, SP-A1/SP-A2 and TNF-a expression were found to be significantly increased in HK-2 cells upon LPS treatment. Transfection of LPS-treated HK-2 cells with SP-A siRNA resulted in significant increases in the levels of NF-κB P65 protein and TNF-α mRNA and protein compared to those in non-transfected LPS-treated HK-2 cells. CONCLUSION: SP-A plays an important role in protecting cells against sepsis-induced acute kidney injury by inhibiting NF-κB activity to modulate LPS-induced increase in TNF-α expression.
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Authors | Jiao Liu, Zhiyong Liu, Lizhi Feng, Guohua Ding, Dechang Chen, Qingshan Zhou |
Journal | Chinese medical journal
(Chin Med J (Engl))
Vol. 127
Issue 2
Pg. 343-7
( 2014)
ISSN: 2542-5641 [Electronic] China |
PMID | 24438626
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Lipopolysaccharides
- Pulmonary Surfactant-Associated Protein A
- SFTPA1 protein, human
- Tumor Necrosis Factor-alpha
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Topics |
- Cell Line
- Epithelial Cells
(cytology, drug effects, metabolism)
- Fluorescent Antibody Technique, Indirect
- Humans
- Kidney Tubules, Proximal
(cytology)
- Lipopolysaccharides
(pharmacology)
- Pulmonary Surfactant-Associated Protein A
(metabolism, pharmacology)
- Tumor Necrosis Factor-alpha
(metabolism)
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