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人角质形成细胞小鼠移植模型中整合素与基底膜的正常化——对表皮稳态的意义

Integrin and basement membrane normalization in mouse grafts of human keratinocytes--implications for epidermal homeostasis.

作者信息

Breitkreutz D, Stark H J, Mirancea N, Tomakidi P, Steinbauer H, Fusenig N E

机构信息

Division of Carcinogenesis and Differentiation, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Differentiation. 1997 Feb;61(3):195-209. doi: 10.1046/j.1432-0436.1997.6130195.x.

Abstract

Integrin patterns and formation of basement membrane (BM) were investigated in correlation to epidermal growth and differentiation during skin regeneration in human keratinocyte transplants on nude mice. Immuno-fluorescence and transmission electron microscopy (TEM) showed that different stages of tissue reconstruction were characterized by a sequence of coordinated events. Features of the initial tissue activation, with rapid keratinocyte proliferation around day 4, including cells in a suprabasal position, were: (1) a marked increase in and extended distribution of the integrin chains alpha 2, alpha 3, beta 1 and alpha 6, while beta 4 already showed a preferential basal location; (2) de novo expression of alpha 5 and alpha v; and (3) marked deposition of laminin-5 and nidogen but low levels of other BM components. Tissue normalization during the 2nd week, initiated by a drastic decrease in the number of proliferating cells after day 4, now strictly in basal position, was signified: by (1) orthotopic staining for basal-type keratins (K5, K14) together with a regular pericellular alpha 2 beta 1 and alpha 3 beta 1 distribution, (2) linear, balanced deposition of BM components (e.g. laminin-1, type IV collagen) and (3) colocalization of integrin alpha 6 beta 4 and bullous pemphigoid antigen. Simultaneously at 7 days hemidesmosomes and a defined BM had developed (TEM), becoming continuous at 14 days. This coincided with the regular distribution of suprabasal keratins (K1, K10) as well as intermediate (involucrin) and late differentiation markers (filaggrin, loricrin). Type-VII collagen deposition, still irregular at 14 days, became continuous at 22 days together with developing BM-anchoring fibrils indicating final tissue consolidation. This model mimics principal stages of epidermal wound healing in human skin and implies a linkage between BM assembly, integrin distribution and the compartment of proliferation competent cells, which in turn determines the onset of differentiation. Thus, apart from the balance of diffusible growth regulators, this positional control of keratinocytes, largely accomplished by integrin-matrix interactions, seems to be prerequisite to establishment and maintenance of tissue homeostasis.

摘要

在裸鼠的人角质形成细胞移植皮肤再生过程中,研究了整合素模式和基底膜(BM)形成与表皮生长和分化的相关性。免疫荧光和透射电子显微镜(TEM)显示,组织重建的不同阶段以一系列协调事件为特征。初始组织激活的特征,在第4天左右角质形成细胞快速增殖,包括基底上层的细胞,表现为:(1)整合素链α2、α3、β1和α6显著增加且分布扩展,而β4已显示出优先的基底定位;(2)α5和αv的从头表达;(3)层粘连蛋白-5和巢蛋白的显著沉积,但其他BM成分水平较低。第2周的组织正常化,由第4天后增殖细胞数量急剧减少引发,此时细胞严格处于基底位置,表现为:(1)基底型角蛋白(K5、K14)的原位染色以及规则的细胞周围α2β1和α3β1分布;(2)BM成分(如层粘连蛋白-1、IV型胶原)的线性、平衡沉积;(3)整合素α6β4和大疱性类天疱疮抗原的共定位。同时在7天时半桥粒和明确的BM已形成(TEM),在14天时变得连续。这与基底上层角蛋白(K1、K10)以及中间(兜甲蛋白)和晚期分化标志物(丝聚蛋白、loricrin)的规则分布一致。VII型胶原沉积在14天时仍不规则,在22天时与发育中的BM锚定原纤维一起变得连续,表明组织最终巩固。该模型模拟了人类皮肤表皮伤口愈合的主要阶段,并暗示了BM组装、整合素分布与增殖能力细胞区室之间的联系,这反过来又决定了分化的开始。因此,除了可扩散生长调节剂之间的平衡外,这种主要由整合素-基质相互作用完成的角质形成细胞的位置控制,似乎是建立和维持组织稳态的先决条件。

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