Hirai Maretoshi, Ohbayashi Tetsuya, Horiguchi Masahito, Okawa Katsuya, Hagiwara Akari, Chien Kenneth R, Kita Toru, Nakamura Tomoyuki
Horizontal Medical Research Organization, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.
J Cell Biol. 2007 Mar 26;176(7):1061-71. doi: 10.1083/jcb.200611026. Epub 2007 Mar 19.
Elastic fibers are required for the elasticity and integrity of various organs. We and others previously showed that fibulin-5 (also called developing arteries and neural crest EGF-like [DANCE] or embryonic vascular EGF-like repeat-containing protein [EVEC]) is indispensable for elastogenesis by studying fibulin-5-deficient mice, which recapitulate human aging phenotypes caused by disorganized elastic fibers (Nakamura, T., P.R. Lozano, Y. Ikeda, Y. Iwanaga, A. Hinek, S. Minamisawa, C.F. Cheng, K. Kobuke, N. Dalton, Y. Takada, et al. 2002. Nature. 415:171-175; Yanagisawa, H., E.C. Davis, B.C. Starcher, T. Ouchi, M. Yanagisawa, J.A. Richardson, and E.N. Olson. 2002. Nature. 415:168-171). However, the molecular mechanism by which fiblin-5 contributes to elastogenesis remains unknown. We report that fibulin-5 protein potently induces elastic fiber assembly and maturation by organizing tropoelastin and cross-linking enzymes onto microfibrils. Deposition of fibulin-5 on microfibrils promotes coacervation and alignment of tropoelastins on microfibrils, and also facilitates cross-linking of tropoelastin by tethering lysyl oxidase-like 1, 2, and 4 enzymes. Notably, recombinant fibulin-5 protein induced elastogenesis even in serum-free conditions, although elastogenesis in cell culture has been believed to be serum-dependent. Moreover, the amount of full-length fibulin-5 diminishes with age, while truncated fibulin-5, which cannot promote elastogenesis, increases. These data suggest that fibulin-5 could be a novel therapeutic target for elastic fiber regeneration.
弹性纤维是各种器官弹性和完整性所必需的。我们和其他人之前通过研究纤连蛋白-5缺陷小鼠发现,纤连蛋白-5(也称为发育中的动脉和神经嵴表皮生长因子样蛋白[DANCE]或含胚胎血管表皮生长因子样重复序列的蛋白[EVEC])对于弹性纤维生成是不可或缺的,这些小鼠重现了由紊乱的弹性纤维引起的人类衰老表型(中村,T.,P.R.洛萨诺,Y.池田,Y.岩永,A.希内克,S.水泽,C.F.程,K.小布,N.道尔顿,Y.高田等人。2002年。《自然》。415:171 - 175;柳泽,H.,E.C.戴维斯,B.C.斯塔彻,T.大内,M.柳泽,J.A.理查森,和E.N.奥尔森。2002年。《自然》。415:168 - 171)。然而,纤连蛋白-5促进弹性纤维生成的分子机制仍然未知。我们报告纤连蛋白-5蛋白通过将原弹性蛋白和交联酶组织到微原纤维上,有力地诱导弹性纤维组装和成熟。纤连蛋白-5在微原纤维上的沉积促进原弹性蛋白在微原纤维上的凝聚和排列,并且还通过束缚赖氨酰氧化酶样1、2和4酶促进原弹性蛋白的交联。值得注意的是,重组纤连蛋白-5蛋白即使在无血清条件下也能诱导弹性纤维生成,尽管细胞培养中的弹性纤维生成一直被认为是依赖血清的。此外,全长纤连蛋白-5的量随着年龄增长而减少,而不能促进弹性纤维生成的截短型纤连蛋白-5增加。这些数据表明纤连蛋白-5可能是弹性纤维再生的一个新的治疗靶点。