Verschuure Pauline, Tatard Caroline, Boelens Wilbert C, Grongnet Jean-François, David Jean Claude
Department of Biochemistry, 161 Nijmegen Center for Molecular Life Sciences, University of Nijmegen, Nijmegen, The Netherlands.
Eur J Cell Biol. 2003 Oct;82(10):523-30. doi: 10.1078/0171-9335-00337.
Recently, we have described the developmental expression of the small heat shock proteins (sHsps) Hsp27/HspB1 and alphaB-crystallin/HspB5 in different tissues of pigs from almost full-term foetuses to three years old adults (P. Tallot, J. F. Grongnet, J. C. David, Biol. Neonate, 83, 281-288, 2003). The data described in this report extends this study to four other members of the sHsp family (Hsp20/HspB6, cvHsp/HspB7, MKBP/HspB2 and HspB8). We studied expression of these proteins in porcine lens, brain, heart, liver, kidney, lung, skeletal muscle, stomach, and colon, and found a ubiquitous expression of Hsp20 and HspB8 as earlier reported for Hsp27 and alphaB-crystallin. In contrast, cvHsp and HspB2 expression is essentially restricted to heart and muscle. During development, the sHsps tend to (temporarily) increase in stomach, liver, lung, kidney, hippocampus, and striatum, while expression in heart is more or less constant, and a large variation is found in sHsp expression patterns in skeletal muscle. In cerebellum and cortex a temporary decrease of Hsp20 and HspB8 is observed directly after birth. The major impact of this study is that each tissue seems to have a unique profile of sHsp expression, which varies during development and may reflect the need of a particular tissue to maintain at all stages an optimal chaperoning machinery to protect against physiological stress.
最近,我们已经描述了小热休克蛋白(sHsps)Hsp27/HspB1和αB-晶状体蛋白/HspB5在从几乎足月胎儿到三岁成年猪的不同组织中的发育表达情况(P. Tallot、J. F. Grongnet、J. C. David,《新生儿生物学》,83卷,281 - 288页,2003年)。本报告中描述的数据将这项研究扩展到了sHsp家族的其他四个成员(Hsp20/HspB6、cvHsp/HspB7、MKBP/HspB2和HspB8)。我们研究了这些蛋白在猪的晶状体、脑、心脏、肝脏、肾脏、肺、骨骼肌、胃和结肠中的表达,发现Hsp20和HspB8存在普遍表达,这与之前报道的Hsp27和αB-晶状体蛋白的情况相同。相比之下,cvHsp和HspB2的表达基本上局限于心脏和肌肉。在发育过程中,sHsps在胃、肝脏、肺、肾脏、海马体和纹状体中倾向于(暂时)增加,而心脏中的表达或多或少保持恒定,并且在骨骼肌中发现sHsp表达模式存在很大差异。在小脑和皮层中,出生后立即观察到Hsp20和HspB8的暂时下降。这项研究的主要影响在于,每个组织似乎都有独特的sHsp表达谱,其在发育过程中会发生变化,这可能反映了特定组织在所有阶段维持最佳伴侣机制以抵御生理应激的需求。