role of visfatin on the regulation of inflammation and apoptosis in the spleen of LPS-treated rats

• Published in: Cell and tissue research 2015-02, Vol.359 (2), p.605-618
• Main Authors: Xiao, Ke, Zou, Wei-Hua, Yang, Zhi, Rehman, Zia ur, Ansari, Abdur Rahman, Yuan, Huai-Rui, Zhou, Ying, Cui, Lu, Peng, Ke-Mei, Song, Hui
• Format: Article
• Language: English
• Subjects: Animals; Antigens, CD - metabolism; Antigens, Differentiation, Myelomonocytic - metabolism; Apoptosis; B cells; bcl-2-Associated X Protein - genetics; bcl-2-Associated X Protein - metabolism; Biomedical and Life Sciences; Biomedicine; Caspase 3 - genetics; Caspase 3 - metabolism; caspase-3; Cytokines; Cytokines - metabolism; Disease Models, Animal; Enzyme-Linked Immunosorbent Assay; genes; Human Genetics; image analysis; Immunohistochemistry; Inflammation; Inflammation - pathology; Inflammation Mediators - metabolism; interleukin-10; interleukin-1beta; interleukin-4; interleukin-6; Lipopolysaccharides - pharmacology; lymphocytes; Lymphocytes - drug effects; Lymphocytes - metabolism; macrophages; Macrophages - drug effects; Macrophages - metabolism; Mitochondria - drug effects; Mitochondria - metabolism; Molecular Medicine; nicotinamide phosphoribosyltransferase; Nicotinamide Phosphoribosyltransferase - metabolism; Protein expression; Proteomics; quantitative polymerase chain reaction; rats; Rats, Wistar; Regular Article; Rodents; Signal Transduction - drug effects; Spleen; Spleen - drug effects; Spleen - enzymology; Spleen - pathology; tumor necrosis factor-alpha; Western blotting
• ISSN: 0302-766X; 1432-0878
• DOI: 10.1007/s00441-014-1997-3

The purpose of the present study is to determine if visfatin is involved in inflammation or apoptosis induced by LPS in rat. Forty Wistar rats were divided into four groups: saline group, LPS group, visfatin group and Visfatin + LPS co-stimulated group. Spleen samples from each group of rats were collected for study. The spleen structure was examined by histological imaging. Apoptosis was evaluated with TUNEL reaction. Caspase-3 was detected with immunohistochemistry and western blot. The apoptosis-related genes were detected by qPCR and inflammatory cytokines were tested by ELISA. Our main findings were as follows. (1) Macrophages were markedly increased in the visfatin group compared with the saline group. This finding was confirmed when spleen samples were examined with western blot using CD68 antibody. (2) Visfatin promoted the expression of CD68 and caspase-3 in rat spleen, whereas visfatin could inhibit the expression of CD68 and activated caspase-3 in spleen of LPS-induced acute inflammation. (3) Visfatin had a pro-apoptotic effect on normal rat spleen, whereas it exerted an anti-apoptotic effect during LPS-induced lymphocytes apoptosis in rat spleen. Moreover, the effect of visfatin on cell apoptosis was mediated by the mitochondrial pathway. (4) Visfatin could modulate both the anti-inflammatory cytokines and pro-inflammatory cytokines in rat spleen, such as IL-10, IL-4, IL-6, TNF-α and IL-1β. Taken together, we demonstrate that visfatin could participate in the inflammatory process in rat spleen by modulating the macrophages and inflammatory cytokines. Also, visfatin plays a dual role in the apoptosis in rat spleen, which is mediated by the mitochondrial pathway.