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在器官型共培养系统中角质形成细胞分化过程中尿激酶型纤溶酶原激活剂(uPA)、其受体(uPA-R)和2型抑制剂(PAI-2)的差异表达。

Differential expression of urokinase-type plasminogen activator (uPA), its receptor (uPA-R), and inhibitor type-2 (PAI-2) during differentiation of keratinocytes in an organotypic coculture system.

作者信息

Schaefer B M, Stark H J, Fusenig N E, Todd R F, Kramer M D

机构信息

Institut für Immunologie der Universität, Laboratorium für Immunpathologie, Heidelberg, Germany.

出版信息

Exp Cell Res. 1995 Oct;220(2):415-23. doi: 10.1006/excr.1995.1333.

Abstract

Cultured keratinocytes resemble migrating keratinocytes under conditions of reepithelialization during wound healing. Such keratinocytes express urokinase-type plasminogen activator (uPA) and its specific receptor (uPA receptor). Receptor-bound uPA activates plasminogen, thus providing plasmin for pericellular proteolysis. uPA is regulated by the plasminogen activator inhibitors PAI-1 and PAI-2. As indicated by immunohistology, neither uPA nor uPA receptor is expressed in normal epidermis. Thus, the down-regulation of uPA and uPA-receptor expression in keratinocytes appears to be an important event in epidermal healing and restoration of a normal epidermal tissue architecture. We have addressed this matter by using a culture and differentiation system for keratinocytes in vitro. Keratinocytes were grown in organotypic cocultures for 4, 7, and 14 days. Frozen sections were analyzed with indirect immunofluorescence staining and overlay zymography, the latter detecting activity of plasminogen activators. While tPA and PAI-1 stainings were consistently negative over the entire observation period, uPA and uPA receptor were expressed by basal keratinocytes at Days 4 and 7, but not at Day 14. Accordingly, overlay zymography revealed uPA activity at Days 4 and 7. PAI-2 was found throughout the entire observation period, but with varying distribution: at Days 4 and 7 all suprabasal keratinocytes stained positive for PAI-2. At Day 14, PAI-2-specific stainings were confined to the uppermost cells of the stratum spinosum. Our data demonstrate that uPA and uPA receptor, which are up-regulated in cultured keratinocytes, are down-regulated upon restoration of an epidermis-like structure. The distribution of PAI-2 varied over the observation period and at Day 14 resembled the distribution of PAI-2 in normal epidermis. Taken together, keratinocytes in organotypic coculture behave like keratinocytes in healing wounds in vivo with respect to the expression of the plasminogen activator system.

摘要

在伤口愈合的再上皮化过程中,培养的角质形成细胞类似于迁移的角质形成细胞。这类角质形成细胞表达尿激酶型纤溶酶原激活剂(uPA)及其特异性受体(uPA受体)。与受体结合的uPA激活纤溶酶原,从而为细胞周围的蛋白水解提供纤溶酶。uPA受纤溶酶原激活剂抑制剂PAI-1和PAI-2的调节。免疫组织学表明,正常表皮中既不表达uPA也不表达uPA受体。因此,角质形成细胞中uPA和uPA受体表达的下调似乎是表皮愈合和正常表皮组织结构恢复中的一个重要事件。我们通过使用角质形成细胞的体外培养和分化系统来研究这个问题。角质形成细胞在器官型共培养中培养4天、7天和14天。用间接免疫荧光染色和叠加酶谱法分析冰冻切片,后者检测纤溶酶原激活剂的活性。虽然在整个观察期内tPA和PAI-1染色始终为阴性,但在第4天和第7天,基底角质形成细胞表达uPA和uPA受体,而在第14天则不表达。相应地,叠加酶谱法在第4天和第7天显示出uPA活性。在整个观察期内均发现了PAI-2,但其分布有所不同:在第4天和第7天,所有基底上层角质形成细胞PAI-2染色呈阳性。在第14天,PAI-2特异性染色局限于棘层的最上层细胞。我们的数据表明,在培养的角质形成细胞中上调的uPA和uPA受体,在恢复表皮样结构时会下调。在观察期内,PAI-2的分布有所变化,在第14天类似于正常表皮中PAI-2的分布。综上所述,就纤溶酶原激活剂系统的表达而言,器官型共培养中的角质形成细胞的行为类似于体内愈合伤口中的角质形成细胞。

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