https://scholars.lib.ntu.edu.tw/handle/123456789/569928
標題: | Sirtuin 6 suppresses hypoxia-induced inflammatory response in human osteoblasts via inhibition of reactive oxygen species production and glycolysis—A therapeutic implication in inflammatory bone resorption | 作者: | Hou K.-L. SZE-KWAN LIN Chao L.-H. EDDIE HSIANG HUA LAI Chang C.-C. CHIA-TUNG SHUN Lu W.-Y. JYH-HORNG WANG Hsiao M. Hong C.-Y. SANG-HENG KOK |
公開日期: | 2017 | 出版社: | Blackwell Publishing Inc. | 卷: | 43 | 期: | 2 | 起(迄)頁: | 170-180 | 來源出版物: | BioFactors | 摘要: | Elevated glycolytic activity and redox imbalance induced by tissue hypoxia are common phenomena of chronic inflammation, including inflammatory bone diseases such as arthritis. However, relation between glycolysis and redox signaling in the inflammatory milieu is unclear. The histone deacetylase sirtuin 6 (SIRT6) is a crucial modulator of inflammation and glucose metabolism, and it is also involved in cellular protection against oxidative injury. The aims of the study were to examine the connection between glycolysis and reactive oxygen species (ROS) production in human osteoblastic cells (HOB) and whether SIRT6 modulates inflammatory response via regulation of glycolytic activity and ROS generation. In HOB cultured under hypoxia, expression of lactate dehydrogenase A (LDHA), lactate production and ROS generation were examined. The reciprocal effects between lactate and ROS production and their impact on inflammatory cytokine induction were assessed. The action of SIRT6 on the above reactions was determined. In a rat model of collagen-induced arthritis (CIA), the relation between inflammatory activity and osteoblastic expression of LDHA, level of oxidative lesions, Cyr61 synthesis and macrophage recruitment were examined in joints with or without lentiviral-SIRT6 gene therapy. Results showed that hypoxia stress enhanced lactate and LDHA production in HOB. ROS generation was also increased, and there was a positive feedback between glycolysis and ROS formation. Overexpression of SIRT6 attenuated hypoxia-enhanced glycolysis and ROS generation. Hypoxia-induced expressions of Cyr61, TNF-α, IL-1β, and IL-6 were suppressed by SIRT6 and the inhibitory effects overlapped with antiglycolytic and antioxidation mechanisms. In the model of CIA, forced expression of SIRT6 ameliorated disease progression, osteoblastic synthesis of Cyr61, and macrophage recruitment. More importantly, expression of LDHA and oxidative lesions were decreased in osteoblasts of SIRT6-treated joints. Our findings suggest that SIRT6 suppresses inflammatory response in osteoblasts via modulation of glucose metabolism and redox homeostasis. SIRT6-based strategy may possess therapeutic potential for inflammatory bone resorption. ? 2016 BioFactors, 43(2):170–180, 2017. ? 2016 International Union of Biochemistry and Molecular Biology |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84982224430&doi=10.1002%2fbiof.1320&partnerID=40&md5=6f87b7b755a387c1998a1fd7c04f3e9f https://scholars.lib.ntu.edu.tw/handle/123456789/569928 |
ISSN: | 0951-6433 | DOI: | 10.1002/biof.1320 | SDG/關鍵字: | CD68 antigen; cysteine rich protein 61; double stranded DNA; glyceraldehyde 3 phosphate dehydrogenase; interleukin 1beta; interleukin 6; lactate dehydrogenase; lactic acid; lentivirus vector; messenger RNA; reactive oxygen metabolite; sirtuin 6; tumor necrosis factor; cysteine rich protein 61; isoenzyme; lactate dehydrogenase; lactate dehydrogenase 5; reactive oxygen metabolite; SIRT6 protein, human; sirtuin; sirtuin 6, rat; animal cell; animal experiment; animal model; animal tissue; ankle arthritis; Article; bone atrophy; bone marrow cell; cell culture; controlled study; cytokine production; disease course; drug effect; enzyme activity; glucose metabolism; glycolysis; human; human cell; hypoxia; in vivo gene transfer; inflammation; macrophage; male; nonhuman; osteoblast; osteolysis; positive feedback; primary culture; priority journal; protein expression; protein synthesis; rat; viral gene therapy; animal; biosynthesis; cell hypoxia; cell protection; experimental arthritis; genetics; glycolysis; inflammation; metabolism; osteoblast; osteolysis; pathology; Animals; Arthritis, Experimental; Bone Resorption; Cell Hypoxia; Cysteine-Rich Protein 61; Cytoprotection; Glycolysis; Humans; Inflammation; Isoenzymes; L-Lactate Dehydrogenase; Osteoblasts; Rats; Reactive Oxygen Species; Sirtuins |
顯示於: | 臨床牙醫學研究所 |
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