Disturbed secretion of mutant adiponectin associated with the metabolic syndrome

被引:59
作者
Kishida, K [1 ]
Nagaretani, H [1 ]
Kondo, H [1 ]
Kobayashi, H [1 ]
Tanaka, S [1 ]
Maeda, N [1 ]
Nagasawa, A [1 ]
Hibuse, T [1 ]
Ohashi, K [1 ]
Kumada, M [1 ]
Nishizawa, H [1 ]
Okamoto, Y [1 ]
Ouchi, N [1 ]
Maeda, K [1 ]
Kihara, S [1 ]
Funahashi, T [1 ]
Matsuzawa, Y [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Internal Med & Mol Sci, Suita, Osaka 5650871, Japan
关键词
adipocytokines; adiponectin; hypoadiponectinemia; the metabolic syndrome; secretion; oligomer;
D O I
10.1016/S0006-291X(03)00940-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adiponectin, an adipocyte-derived protein, consists of collagen-like fibrous and complement C1q-like globular domains, and circulates in human plasma in a multimeric form. The protein exhibits anti-diabetic and anti-atherogenic activities. However, adiponectin plasma concentrations are low in obese subjects, and hypoadiponectinemia is associated with the metabolic syndrome, which is a cluster of insulin resistance, type 2 diabetes mellitus, hypertension, and dyslipidemia. We have recently reported a missense mutation in the adiponectin gene, in which isoleucine at position 164 in the globular domain is substituted with threonine (I164T). Subjects with this mutation showed markedly low level of plasma adiponectin and clinical features of the metabolic syndrome. Here, we examined the molecular characteristics of the mutant protein associated with a genetic cause of hypoadiponectinemia. The current study revealed (1) the mutant protein showed an oligomerization state similar to the wild-type as determined by gel filtration chromatography and, (2) the mutant protein exhibited normal insulin-sensitizing activity, but (3) pulse-chase study showed abnormal secretion of the mutant protein from adipose tissues. Our results suggest that I164T mutation is associated with hypoadiponectinemia through disturbed secretion into plasma, which may contribute to the development of the metabolic syndrome. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:286 / 292
页数:7
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