Mutation of the RGD sequence does not affect plasma membrane association and growth inhibitory effects of elevated IGFBP-2 in vivo

被引:29
作者
Hoeflich, A
Reisinger, R
Vargas, GA
Elmlinger, MW
Schuett, B
Jehle, PM
Renner-Müller, I
Lahm, H
Russo, VC
Wolf, E
机构
[1] Univ Munich, Inst Mol Anim Breeding, Gene Ctr, D-81377 Munich, Germany
[2] Dept Internal Med, D-89081 Ulm, Germany
[3] Univ Tubingen, D-72076 Tubingen, Germany
[4] Murdoch Childrens Res Inst, Ctr Hormone Res, Parkville, Vic 3052, Australia
关键词
insulin-like growth factor-binding protein-2; overexpression; transgenic mouse; cell surface association; RGD sequence;
D O I
10.1016/S0014-5793(02)02935-6
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
Using insulin-like growth factor-binding protein-2 (IGFBP-2) transgenic mice (D mice) as a model of elevated IGFBP-2 expression, which is often found in unphysiological conditions, we found association of IGFBP-2 to purified plasma membranes of many organs. To determine whether the RGD (Arg-Gly-Asp) motif of IGFBP-2 mediates cell surface binding in vivo, we mutated the RGD motif of IGFBP-2 into an RGE (Arg-Gly-Glu) sequence and produced transgenic mice (E mice) which express elevated amounts of mutated IGFBP-2. Our data demonstrate that in vivo IGFBP-2 cell surface association is not dependent on the RGD motif and that mutation of this sequence does not alter growth inhibitory effects of IGFBP-2. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:63 / 67
页数:5
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