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小鼠诱导性多能干细胞诱导成骨分化的初步研究 被引量:1
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作者 钱浩 徐增琦 +6 位作者 李杨 徐镭 程杰 江宏兵 吴煜农 jake chen 叶金海 《口腔生物医学》 2015年第4期193-197,共5页
目的:研究小鼠诱导性多能干细胞(induced pluripotent stem cells,i PSCs)向成骨细胞分化的能力,并观察Osterix对i PSCs成骨分化能力的影响。方法:利用体外细胞培养和病毒转染的方法,结合定量RT-PCR以及组织化学的方法检测在成骨诱导的... 目的:研究小鼠诱导性多能干细胞(induced pluripotent stem cells,i PSCs)向成骨细胞分化的能力,并观察Osterix对i PSCs成骨分化能力的影响。方法:利用体外细胞培养和病毒转染的方法,结合定量RT-PCR以及组织化学的方法检测在成骨诱导的条件下,i PSCs中成骨相关基因、蛋白的表达变化。结果:小鼠i PSCs经悬滴培养可以形成拟胚体,在成骨诱导条件下可以向成骨细胞分化。病毒转染并不影响i PSCs的多向分化潜能;与对照组相比,转染Osterix的i PSCs形成的矿化结节、碱性磷酸酶活性、成骨相关基因的表达均有明显增加(P<0.05)。结论:在成骨诱导液培养条件下,小鼠i PSCs可以作为种子细胞向成骨细胞分化,并且过表达转录因子Osterix可以进一步促进i PSCs的成骨分化。 展开更多
关键词 诱导性多能干细胞 OSTERIX 成骨分化 组织工程学 小鼠
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Exercise-induced irisin in bone and systemic irisin administration reveal new regulatory mechanisms of bone metabolism 被引量:26
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作者 Jin Zhang Paloma Valverde +9 位作者 Xiaofang Zhu Dana Murray Yuwei Wu Liming Yu Hua Jiang Michel M Dard Jin Huang Zhiwei Xu Qisheng Tu jake chen 《Bone Research》 SCIE CAS CSCD 2017年第1期49-62,共14页
Irisin is a polypeptide hormone derived from the proteolytic cleavage of fibronectin-type III domain- containing 5 (FNDC5) protein. Once released to circulation upon exercise or cold exposure, irisin stimulates brow... Irisin is a polypeptide hormone derived from the proteolytic cleavage of fibronectin-type III domain- containing 5 (FNDC5) protein. Once released to circulation upon exercise or cold exposure, irisin stimulates browning of white adipose tissue (WAT) and uncoupling protein I (UCP1) expression, leading to an increase in total body energy expenditure by augmented UCPl-mediated thermogenesis. It is currently unknown whether irisin is secreted by bone upon exercise or whether it regulates bone metabolism in vivo. In this study, we found that 2 weeks of voluntary wheel-running exercise induced high levels of FNDC5 messenger RNA as well as FNDC5/irisin protein expression in murine bone tissues. Increased immunoreactivity due to exercise-induced FNDC5/irisin expression was detected in different regions of exercised femoral bones, including growth plate, trabecular bone, cortical bone, articular cartilage, and bone-tendon interface. Exercise also increased expression of osteogenic markers in bone and that of UCP1 in WAT, and led to bodyweight loss. Irisin intraperitoneal (IP) administration resulted in increased trabecular and cortical bone thickness and osteoblasts numbers, and concurrently induced UCP1 expression in subcutaneous WAT. Lentiviral FNDC5 IP administration increased cortical bone thickness. In vitro studies in bone cells revealed irisin increases osteoblastogenesis and mineralization, and inhibits receptor activator of nuclear factor-kB ligand (RANKL)- induced osteoclastogenesis. Taken together, our findings show that voluntary exercise increases irisin production in bone, and that an increase in circulating irisin levels enhances osteogenesis in mice. 展开更多
关键词 Exercise-induced irisin in bone and systemic irisin administration reveal new regulatory mechanisms of bone metabolism BONE
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