Differential onset of expression of alpha 7 and beta 1D integrins during mouse heart and skeletal muscle development.

M Brancaccio, S Cabodi, A M Belkin, G Collo, V E Koteliansky, D Tomatis, F Altruda, L Silengo, G Tarone
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引用次数: 49

Abstract

beta 1D is a recently identified isoform of the beta 1 integrin subunit selectively expressed in skeletal and cardiac muscles. In the present study we determined the temporal expression of beta 1D and its association with alpha subunits during mouse development. By immunohistochemistry and western blot analysis we demonstrated that beta 1D begins to be expressed in skeletal muscles of 17 days embryo (stage E17). Its level progressively increases reaching maximal values few days after birth and remaining high in adult mice. At earlier stages of development (E11-E17) the beta 1A isoform is expressed in skeletal muscle cells. After E17 beta 1A is downregulated and disappears from muscle fibers few days after birth. In cardiac muscle the regulation of the beta 1D expression is different: beta 1D and beta 1A are coexpressed in the heart of E11 embryo. Subsequently expression of beta 1A declines, while beta 1D increases until it becomes the unique beta 1 isoform in cardiomyocytes few days after birth. Previous studies (Belkin et al J. Cell Biol. 132: 211-226, 1996) demonstrated that beta 1D in adult mouse cardiomyocytes is exclusively associated with alpha 7B. Western blot analysis shows that alpha 7B starts to be expressed in the heart only at stage E17, while beta 1D is expressed already at E11 embryo, indicating that alpha subunits other than alpha 7 should associate with beta 1D in early developmental stages. To investigate this aspect, beta 1 associated alpha subunits were identified by western blotting from cardiomyocytes integrin complexes immunoprecipitated with alpha subunit specific antibodies. We found that, during cardiomyocyte development, beta 1D associates with several alpha subunits namely with alpha 5, alpha 6A and alpha 7B. In conclusion these data show that the expression of the beta 1D muscle specific integrin during development occurs much earlier in heart than in skeletal muscle and it can dimerize with different alpha subunits.

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α 7和β 1D整合素在小鼠心脏和骨骼肌发育过程中的表达差异
β 1D是最近发现的β 1整合素亚基在骨骼肌和心肌中选择性表达的亚型。在本研究中,我们确定了在小鼠发育过程中β 1D的时间表达及其与α亚基的关联。通过免疫组化和western blot分析,我们发现β 1D在胚胎第17天(E17期)的骨骼肌中开始表达。它的水平逐渐增加,在出生后几天达到最大值,并在成年小鼠中保持高水平。在早期发育阶段(E11-E17), β 1A亚型在骨骼肌细胞中表达。E17后β 1A被下调,并在出生后几天从肌纤维中消失。在心肌中β 1D表达的调控是不同的:β 1D和β 1A在E11胚胎的心脏中共表达。随后β 1A的表达下降,而β 1D的表达增加,直到出生后几天成为心肌细胞中独特的β 1亚型。先前的研究(Belkin et al . Cell Biol. 132: 211- 226,1996)表明,成年小鼠心肌细胞中的β 1D仅与α 7B相关。Western blot分析显示,α - 7B仅在E17期开始在心脏中表达,而β - 1D在E11期胚胎中就已经表达,这表明α - 7以外的α亚基可能在早期发育阶段与β - 1D相关。为了研究这方面的问题,通过western blotting从心肌细胞整合素复合物中鉴定出β 1相关的α亚基,这些整合素复合物与α亚基特异性抗体免疫沉淀。我们发现,在心肌细胞发育过程中,β 1D与几个α亚基,即α 5、α 6A和α 7B相关联。综上所述,这些数据表明β 1D肌肉特异性整合素在心脏发育过程中的表达比在骨骼肌中的表达要早得多,并且它可以与不同的α亚基二聚。
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