Kaplan E D, Holbrook K A
Department of Biological Structure, University of Washington School of Medicine, Seattle 98195.
Dev Dyn. 1994 Feb;199(2):141-55. doi: 10.1002/aja.1001990207.
The development of skin appendages such as hair, feathers, and teeth is brought about by reciprocal interactions between epidermal and mesenchymal tissues and is thought to be influenced in part by cell adhesion molecules and components of the extracellular matrix. The developmental distributions of tenascin, neural cell adhesion molecule (NCAM), E-cadherin, intercellular adhesion molecule 1 (ICAM-1), chondroitin sulfate proteoglycan (CSPG), and the heparan sulfate proteoglycan perlecan were studied in relation to hair follicle morphogenesis in fetal human skin. Tenascin first appeared in developing skin in focal concentrations at the epidermal-mesenchymal interface, just prior to, and presumably correlated with, hair follicle initiation. Tenascin immunostaining remained prominent in the basement membrane zone and extracellular matrix of the follicle sheath during subsequent morphogenetic stages. Two forms of tenascin (M(r) 250 x 10(3) and 280-300 x 10(3)), were revealed by Western blots of skin extracts. NCAM immunolabeling was initially present throughout the dermis, and became progressively restricted to the dermal condensation and the follicle sheath. Western blot analysis revealed an isoform of NCAM (M(r) 160 x 10(3)) which lacked polysialic acid. At all stages, E-cadherin staining was diminished on follicle cells situated adjacent to the basement membrane, relative to cells in the follicle interior. Follicle-specific immunostaining for ICAM-1 was transient, appearing only at the pre-germ and hair germ stages of development. Antibodies to three distinct CSPG determinants revealed unique immunolabeling patterns following follicle initiation: One CSPG epitope co-distributed with tenascin in the follicle basement membrane and follicle sheath extracellular matrix; one CSPG epitope was similarly expressed, and was also found on follicle epithelial cells; and the third CSPG determinant was noticeably absent from the follicle sheath during elongation of the developing appendage. Perlecan was concentrated in the dermal papilla, in addition to its distribution in all skin basement membranes. A model for how these diverse molecules may interact to influence human hair follicle morphogenesis is presented.
毛发、羽毛和牙齿等皮肤附属器的发育是由表皮组织和间充质组织之间的相互作用引起的,并且认为部分受细胞粘附分子和细胞外基质成分的影响。研究了腱生蛋白、神经细胞粘附分子(NCAM)、E-钙粘蛋白、细胞间粘附分子1(ICAM-1)、硫酸软骨素蛋白聚糖(CSPG)和硫酸乙酰肝素蛋白聚糖基底膜蛋白聚糖在胎儿皮肤毛囊形态发生过程中的发育分布情况。腱生蛋白首先以局灶性浓度出现在发育中的皮肤表皮-间充质界面,就在毛囊起始之前,并且推测与之相关。在随后的形态发生阶段,腱生蛋白免疫染色在毛囊鞘的基底膜区和细胞外基质中仍然显著。通过皮肤提取物的蛋白质印迹法揭示了两种形式的腱生蛋白(相对分子质量分别为250×10³和280 - 300×10³)。NCAM免疫标记最初存在于整个真皮中,并逐渐局限于真皮凝聚区和毛囊鞘。蛋白质印迹分析显示一种缺乏多唾液酸的NCAM同工型(相对分子质量为160×10³)。在所有阶段,相对于毛囊内部的细胞,位于基底膜附近的毛囊细胞上的E-钙粘蛋白染色减弱。ICAM-1的毛囊特异性免疫染色是短暂的,仅出现在发育的前胚和毛胚阶段。针对三种不同CSPG决定簇的抗体在毛囊起始后显示出独特的免疫标记模式:一种CSPG表位与腱生蛋白在毛囊基底膜和毛囊鞘细胞外基质中共分布;一种CSPG表位有类似表达,并且也在毛囊上皮细胞上发现;在发育中的附属器伸长过程中,第三种CSPG决定簇在毛囊鞘中明显缺失。基底膜蛋白聚糖除了分布在所有皮肤基底膜中外,还集中在真皮乳头中。本文提出了一个关于这些不同分子如何相互作用以影响人类毛囊形态发生的模型。