The bcl-2 knockout mouse exhibits marked changes in osteoblast phenotype and collagen deposition in bone as well as a mild growth plate phenotype

被引:20
作者
Boot-Handford, RP
Michaelidis, TM
Hillarby, MC
Zambelli, A
Denton, J
Hoyland, JA
Freemont, AJ
Grant, ME
Wallis, GA
机构
[1] Univ Manchester, Sch Biol Sci, Wellcome Trust Ctr Cell Matrix Res, Manchester M13 9PT, Lancs, England
[2] Univ Manchester, Sch Biol Sci, Dept Rheumatol, Manchester M13 9PT, Lancs, England
[3] Univ Manchester, Sch Biol Sci, Dept Med, Manchester M13 9PT, Lancs, England
[4] Max Planck Inst Psychiat, Dept Neurochem, D-8033 Martinsried, Germany
基金
英国惠康基金;
关键词
Bcl-2; bcl-2 knockout mouse; growth plate; osteoblast; bone; collagen;
D O I
10.1046/j.1365-2613.1998.790411.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Histological examination of long bones from 1-day-old bcl-2 knockout and age-matched control mice revealed no obvious differences in length of bone, growth plate architecture or stage of endochondral ossification. In 35-day-old bcl-2 knockout mice that are growth retarded or 'dwarfed', the proliferative zone of the growth plate appeared slightly thinner and the secondary centres of ossification less well developed than their age-matched wild-type controls. The most marked histological effects of bcl-2 ablation were on osteoblasts and bone. 35-day-old knockout mouse bones exhibited far greater numbers of osteoblasts than controls and the osteoblasts had a cuboidal phenotype in comparison with the normal flattened cell appearance. In addition, the collagen deposited by the osteoblasts in the bcl-2 knockout mouse bone was disorganized in comparison with control tissue and had a pseudo-woven appearance. The results suggest an important role for Bcl-2 in controlling osteoblast phenotype and bone deposition in vivo.
引用
收藏
页码:329 / 335
页数:7
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