Hart D A, Reno C, Hellio Le Graverand M P, Hoffman L, Kulyk W
McCaig Centre for Joint Injury and Arthritis Research, Faculty of Medicine, University of Calgary, AB, Canada.
Biochem Cell Biol. 2000;78(4):511-8.
Hsp47 (also termed "colligin") is a 47 kDa protein that is localized in the ER and cis-Golgi vesicles of fibrocytes, chondrocytes, and other collagen-secreting cells. Under stress conditions, Hsp47 expression is upregulated as part of the heat shock/stress response that mitigates cell damage from noxious stimuli such as elevated temperature, heavy metals, and oxidative stress. Under non-stress conditions, Hsp47 functions as a collagen-specific molecular chaperone that facilitates intracellular procollagen polypeptide synthesis, and triple helix assembly in connective tissues. Previously it has been shown that levels of collagen-specific gene expression are significantly altered in ligaments, menisci, and other connective tissues of the rabbit following surgically induced injuries (increased), and during pregnancy (decreased). The present study was undertaken to determine whether expression of mRNA for the Hsp47 collagen-binding stress protein was also influenced in these experimental models. Since no sequence information was available on the rabbit Hsp47 gene, a partial cDNA for rabbit Hsp47 was first isolated and cloned using reverse transcriptase PCR (RT-PCR) with degenerate oligonucleotide primers. Rabbit Hsp47 sequence-specific primers then designed enabled analysis of Hsp47 mRNA expression in rabbit connective tissues using semiquantitative RT-PCR. It was found that Hsp47 expression is affected in a complex, tissue-specific manner by injury and pregnancy. Hsp47 transcript levels were elevated in the medial collateral ligament (MCL) of the rabbit knee following surgical induction of a gap injury. Transection of the anterior cruciate ligament (ACL), which leads to chronic progressive damage to menisci of the rabbit knee joint, was accompanied by an upregulation of Hsp47 expression in the medial and lateral menisci. Hsp47 mRNA levels were depressed during pregnancy in the kidney and ACL of primigravid adolescent rabbits, but were not altered in corneal tissue during pregnancy or in the ACL of skeletally mature multiparous females. The changes in Hsp47 transcript levels within these connective tissues following injury/pregnancy often, but not always, paralleled changes in collagen-specific gene expression.
热休克蛋白47(也称为“胶原结合蛋白”)是一种47 kDa的蛋白质,定位于成纤维细胞、软骨细胞和其他分泌胶原蛋白的细胞的内质网和顺式高尔基体囊泡中。在应激条件下,热休克蛋白47的表达上调,作为热休克/应激反应的一部分,减轻诸如高温、重金属和氧化应激等有害刺激对细胞的损伤。在非应激条件下,热休克蛋白47作为一种胶原特异性分子伴侣,促进细胞内前胶原多肽的合成以及结缔组织中三螺旋的组装。此前已表明,在手术诱导损伤后(增加)以及怀孕期间(减少),兔的韧带、半月板和其他结缔组织中胶原特异性基因表达水平发生显著改变。本研究旨在确定热休克蛋白47胶原结合应激蛋白的mRNA表达在这些实验模型中是否也受到影响。由于兔热休克蛋白47基因没有序列信息,首先使用简并寡核苷酸引物通过逆转录聚合酶链反应(RT-PCR)分离并克隆了兔热休克蛋白47的部分cDNA。然后设计的兔热休克蛋白47序列特异性引物能够使用半定量RT-PCR分析兔结缔组织中热休克蛋白47 mRNA的表达。结果发现,热休克蛋白47的表达受到损伤和怀孕的复杂的、组织特异性的影响。在兔膝关节内侧副韧带(MCL)手术诱导间隙损伤后,热休克蛋白47转录水平升高。前交叉韧带(ACL)横断导致兔膝关节半月板慢性进行性损伤,同时内侧和外侧半月板中热休克蛋白47表达上调。初孕青春期兔的肾脏和ACL中热休克蛋白47 mRNA水平在怀孕期间降低,但在怀孕期间角膜组织或骨骼成熟经产雌性动物的ACL中未发生改变。这些结缔组织在损伤/怀孕后热休克蛋白47转录水平的变化通常但并非总是与胶原特异性基因表达的变化平行。