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骨性关节炎软骨和软骨下骨之间信号通路 被引量:14

Signal pathway between cartilage and subchondral bonein osteoarthritis
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摘要 骨性关节炎(osteoarthritis,OA)的发生和发展离不开软骨和软骨下骨共同病变的过程。信号通路的异常在调控OA软骨下骨和软骨的病变中起重要作用。Wnt、转化生长因子β(transforming growth factorβ,TGFβ)/骨形态发生蛋白(bone morphogenetic protein,BMP)、丝裂原活化蛋白激酶(mitogen-activated protein kinases,MAPK)信号通路对骨和软骨正常生长发育和代谢有着重要的调控作用,维持了关节的健康和平衡。研究显示,在OA中,这些信号通路的改变不仅可使OA软骨下骨和软骨的细胞表型和分子功能失衡,细胞外基质的合成破坏,软骨下骨骨重塑,还可通过破坏组织细胞的代谢进一步改变骨和软骨的结构及应力承担能力。因此,本文围绕骨关节炎病变中Wnt、TGFβ/BMP、MAPK信号交流在OA中软骨下骨和软骨病变中的作用和机制进行综述,以期为OA和其他骨关节疾病的研究和治疗提供新的方法和思路。 The occurrence and development of osteoarthritis (OA) can not be separated from the common patho- logical changes of cartilage and subchondral bone. Abnormal signal pathway plays an important role in the regulation of bone and cartilage lesions in OA. Wnt, TGFβ (transforming growth factor β) /BMP (bone morphogenetic protein), MAPK (mitogen-activated protein kinases) signaling pathway plays an important role in the normal growth and metabo- lism of bone and cartilage, maintaining the health and balance of the joints. Studies have shown that in the lesions of os- teoarthritis, these signals can not only make the cell phenotype and molecular function imbalance of OA subchondral bone and cartilage, the synthesis of extracellular matrix distroyed, subchondral bone remodeling, but also destrog the metabo- lism of tissue cells and further change the structure and bear ability of stress of bone and cartilage. Therefore, this review summarizes the role and mechanism of Wnt, TGF/BMP, MAPK signaling of OA on communication between cartilage and subchondral bone, in order to provide new methods and ideas for the research and study of osteoarthritis and other bone diseases.
出处 《中华骨质疏松和骨矿盐疾病杂志》 2016年第2期193-198,共6页 Chinese Journal Of Osteoporosis And Bone Mineral Research
基金 国家自然科学基金面上项目(81572218) 上海市自然科学基金(13ZR1439100) 上海市卫生局局级课题面上项目科研基金(20124303)
关键词 骨关节炎 WNT信号通路 TGFβ/BMP信号通路 MAPK信号通路 osteoarthritis Wnt signaling pathway TGF/BMP signaling pathway MAPK signaling pathway
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  • 1Roel NUSSE.Wnt signaling in disease and in development[J].Cell Research,2005,15(1):28-32. 被引量:86
  • 2Berenbaum F. New horizons and perspectives in the treatment of os- teoarthritis [ J ]. Arthritis Res Ther, 2008,10 ( Suppl 2 ) : S 1.
  • 3Fecher LA,Amaravadi RK,Flaherty KT. The MAPK pathway in melanoma[J]. Curr Opin Oneol,2008,20(2) : 183-189.
  • 4Kimura H,Yukitake H,Suzuki H,et al. The chondroproteetive a- gent ITZ-1 inhibits interleukin-lbeta-induced matrix metallopro- teinase-13 production and suppresses nitric oxide-induced chon- drocyte death [ J ]. J Pharmacol Sei, 2009,110 (2) : 201-211.
  • 5Kim EK, Choi EJ. Pathological roles of MAPK signaling pathways in human diseases [J]. Biochim Biophys Acta,2010,1802(4) :396-405.
  • 6Prasadam I, Friis T, Shi W, et al. Osteoarthritic cartilage chondro- cytes alter subehondral bone osteoblast differentiation via MAPK signalling pathway involving ERK 1/2 [ J ]. Bone, 2010,46 ( 1 ) : 226- 235.
  • 7Chowdhury TT,Salter DM, Bader DL,et al. Signal transduction pathways involving p38 MAPK,JNK,NFkappaB and AP-1 influ- ences the response of chondroeytes cultured in agarose constructs to IL- 1beta and dynamic compression [ J ]. Inflamm Res,2008,57 (7) : 306-313.
  • 8Stoddart M J, Grad S, Eglin D,et al. Cells and biomaterials in carti- lage tissue engineering[ J ]. Regen Med, 2009,4 ( 1 ) : 81-98.
  • 9Murphy G, Kntiuper V,Atkinson S, et al. Matrix metalloproteinases in arthritic disease [ J ]. Arthritis Res, 2002,4 (Suppl 3 ) : S39-49.
  • 10Huang D, Ding Y, Luo WM, et al. Inhibition of MAPK kinase sig- naling pathways suppressed renal cell carcinoma growth and an- giogenesis in vivo [J ]. Cancer Res, 2008,68 ( 1 ) : 81-88.

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