The adipocyte-secreted protein Acrp30 enhances hepatic insulin action

被引:2064
作者
Berg, AH
Combs, TP
Du, XL
Brownlee, M
Scherer, PE [1 ]
机构
[1] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USA
[2] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[3] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10467 USA
[4] Albert Einstein Coll Med, Ctr Diabet Res & Training, Bronx, NY 10467 USA
关键词
D O I
10.1038/90992
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
Acrp30 is a circulating protein synthesized in adipose tissue. A single injection in mice of purified recombinant Acrp30 leads to a 2-3-fold elevation in circulating Acrp30 levels, which triggers a transient decrease in basal glucose levels. Similar treatment in ob/ob, NOD (non-obese diabetic) or streptozotocin-treated mice transiently abolishes hyperglycemia. This effect on glucose is not associated with an increase in insulin levels. Moreover, in isolated hepatocytes, Acrp30 increases the ability of sub-physiological levels of insulin to suppress glucose production. We thus propose that Acrp30 is a potent insulin enhancer linking adipose tissue and whole-body glucose metabolism.
引用
收藏
页码:947 / 953
页数:7
相关论文
共 33 条
[21]   CDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (Adipose most abundant gene transcript 1) [J].
Maeda, K ;
Okubo, K ;
Shimomura, I ;
Funahashi, T ;
Matsuzawa, Y ;
Matsubara, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 221 (02) :286-289
[22]   Caloric restriction and aging: an update [J].
Masoro, EJ .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (03) :299-305
[23]   Green fluorescent protein as a second selectable marker for selection of high producing clones from transfected CHO cells [J].
Meng, YG ;
Liang, J ;
Wong, WL ;
Chisholm, V .
GENE, 2000, 242 (1-2) :201-207
[24]   Adipose tissue as an endocrine and paracrine organ [J].
Mohamed-Ali, V ;
Pinkney, JH ;
Coppack, SW .
INTERNATIONAL JOURNAL OF OBESITY, 1998, 22 (12) :1145-1158
[25]  
Nakano Y, 1996, J BIOCHEM-TOKYO, V120, P803
[26]   Mechanisms by which thiazolidinediones enhance insulin action [J].
Reginato, MJ ;
Lazar, MA .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1999, 10 (01) :9-13
[27]   GENOMIC ORGANIZATION AND FULL-LENGTH CDNA SEQUENCE OF HUMAN COLLAGEN-X [J].
REICHENBERGER, E ;
BEIER, F ;
LUVALLE, P ;
OLSEN, BR ;
VONDERMARK, K ;
BERTLING, WM .
FEBS LETTERS, 1992, 311 (03) :305-310
[28]   COMPLETION OF THE AMINO-ACID-SEQUENCES OF THE A-CHAIN AND B-CHAIN OF SUBCOMPONENT C1Q OF THE 1ST COMPONENT OF HUMAN-COMPLEMENT [J].
REID, KBM ;
GAGNON, J ;
FRAMPTON, J .
BIOCHEMICAL JOURNAL, 1982, 203 (03) :559-569
[29]   A NOVEL SERUM-PROTEIN SIMILAR TO C1Q, PRODUCED EXCLUSIVELY IN ADIPOCYTES [J].
SCHERER, PE ;
WILLIAMS, S ;
FOGLIANO, M ;
BALDINI, G ;
LODISH, HF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26746-26749
[30]   Metabolic impact of adenovirus-mediated overexpression of the glucose-6-phosphatase catalytic subunit in hepatocytes [J].
Seoane, J ;
Trinh, K ;
ODoherty, RM ;
GomezFoix, AM ;
Lange, AJ ;
Newgard, CB ;
Guinovart, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) :26972-26977