Scott G A, Haake A R
Dermatology Department, University of Rochester, New York 14642.
J Invest Dermatol. 1991 Nov;97(5):776-81. doi: 10.1111/1523-1747.ep12486726.
To determine if keratinocytes influence melanocyte number and position in the developing epidermis we have experimentally recombined keratinocytes and melanocytes from epidermis of different stages of differentiation in the skin equivalent (SE) system. Previously we showed that developmental differences in the position and number of melanocytes characteristic of the epidermis in vivo were preserved in fetal and neonatal skin equivalents. In the present study we have combined cultured fetal or neonatal keratinocytes with age-matched or non-age-matched cultured melanocytes on the dermal equivalent. The ratio of basal keratinocytes to melanocytes (BK/M) present in multiple high-power fields was determined after localization of melanocytes by staining with the melanocyte-specific monoclonal antibody, HMB-45. The BK/M ratio in SE composed of neonatal keratinocytes and either fetal (n = 4) or neonatal (n = 5) melanocytes was 26.2 and 21.5, respectively. The BK/M ratio in SE composed of fetal keratinocytes and either fetal (n = 8) or neonatal (n = 5) melanocytes was 9.2 and 7.7, respectively. In each case, the BK/M ratio was dependent on the keratinocytes rather than the melanocytes. With either type of melanocyte, ratios in SE composed of neonatal keratinocytes were significantly greater than those with fetal keratinocytes. These results establish that keratinocytes regulate the BK/M ratio in this model and suggest that developmental differences between fetal and neonatal keratinocytes may be responsible for determining melanocyte numbers in the epidermal-melanin unit in vivo. The precise mechanisms that control the organization and number of melanocytes in the epidermis are unknown although keratinocytes may interact with melanocytes via growth factors, cell surface molecules, or other factors related to proliferation and differentiation of the epidermis.
为了确定角质形成细胞是否会影响发育中表皮内黑素细胞的数量和位置,我们在皮肤替代物(SE)系统中,对来自不同分化阶段表皮的角质形成细胞和黑素细胞进行了实验性重组。此前我们发现,体内表皮特有的黑素细胞在位置和数量上的发育差异,在胎儿和新生儿皮肤替代物中得以保留。在本研究中,我们将培养的胎儿或新生儿角质形成细胞与年龄匹配或不匹配的培养黑素细胞组合在真皮替代物上。在用黑素细胞特异性单克隆抗体HMB - 4进行染色以定位黑素细胞后,测定多个高倍视野中基底角质形成细胞与黑素细胞的比例(BK/M)。由新生儿角质形成细胞和胎儿(n = 4)或新生儿(n = 5)黑素细胞组成的SE中的BK/M比例分别为26.2和21.5。由胎儿角质形成细胞和胎儿(n = 8)或新生儿(n = 5)黑素细胞组成的SE中的BK/M比例分别为9.2和7.7。在每种情况下,BK/M比例取决于角质形成细胞而非黑素细胞。无论使用哪种类型的黑素细胞,由新生儿角质形成细胞组成的SE中的比例均显著高于由胎儿角质形成细胞组成的SE中的比例。这些结果表明,在该模型中角质形成细胞调节BK/M比例,并提示胎儿和新生儿角质形成细胞之间的发育差异可能是决定体内表皮 - 黑素单位中黑素细胞数量的原因。尽管角质形成细胞可能通过生长因子、细胞表面分子或与表皮增殖和分化相关的其他因子与黑素细胞相互作用,但控制表皮中黑素细胞的组织和数量的精确机制尚不清楚。