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International Journal of Experimental Pathology logoLink to International Journal of Experimental Pathology
. 1998 Oct;79(5):329–335. doi: 10.1046/j.1365-2613.1998.790411.x

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

R P BOOT-HANDFORD 1, T M MICHAELIDIS 2, M C HILLARBY 3, A ZAMBELLI 1, J DENTON 3, J A HOYLAND 3, A J FREEMONT 3, M E GRANT 1, G A WALLIS 1,4
PMCID: PMC3220196  PMID: 10193316

Abstract

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.

Keywords: Bcl-2, bcl-2 knockout mouse , growth plate, osteoblast, bone, collagen


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