Matsumoto K, Robb E, Warden G, Nordlund J
POLA Laboratories, Yokohama, Japan.
Exp Dermatol. 1997 Feb;6(1):13-21. doi: 10.1111/j.1600-0625.1997.tb00140.x.
We postulate that wound healing is an orderly process mediated by a programmed expression of cytokines and growth factors. We suggest that these factors are produced in a consistent sequence, in regulated quantities and eliminated when their function is complete. We report here the results of studies on several cytokines, growth factors and the intercellular adhesion molecule expressed during the healing of grafts were visible clinically around 3-5 days post-graft and were completed by 4 weeks post-graft. During the 1st 2 weeks, we observed the following. (i) K-14 keratin was prominent throughout the entire epidermis. Thereafter it was limited to basal cell layers. (ii) Langerhans cells were not detectable with anti-human CD1a antibodies during the first week of healing but were clearly detectable 2 weeks post-graft. (iii) DOPA (dihydroxy phenylalanine) positive melanocytes gradually increased with time. The epidermis 21 to 28 days post-graft clinically and histologically seemed to be morphologically intact. Interleukin-1 (IL-1) was clearly detected in some basal cells of the epidermis, especially in melanocytes and some keratinocytes during the early stage of healing. Transforming growth factor-alpha (TGF-alpha) was detected in epidermis first in melanocytes and some keratinocytes shortly after grafting and again in the late stage of healing. It was also found in some dermal cells. Its expression coincided with keratinocyte proliferation and melanocyte migration. TGF-beta was strongly expressed in the epidermis and dermis after the first week post graft. (iv) ICAM-1 was transiently expressed only at the onset of healing. We previously reported that pro-opiomelanocortin and its derivatives MSH/ ACTH are expressed strongly during the healing of human xenografts. The 4 additional molecules which are the subject of this report all are expressed in healing human skin in a predictable sequence and quantity (intensity of stain). Together these data support our hypothesis that healing is a highly regulated process mediated by numerous cytokines.
我们推测伤口愈合是一个由细胞因子和生长因子的程序性表达介导的有序过程。我们认为这些因子以一致的顺序产生,数量受到调节,并在其功能完成后被清除。我们在此报告了对几种细胞因子、生长因子以及移植物愈合过程中表达的细胞间黏附分子的研究结果。临床上,移植物周围在移植后约3 - 5天可见愈合迹象,并在移植后4周完成。在最初的2周内,我们观察到以下情况。(i) K - 14角蛋白在整个表皮中都很突出。此后它局限于基底细胞层。(ii) 在愈合的第一周,用抗人CD1a抗体检测不到朗格汉斯细胞,但在移植后2周可清楚检测到。(iii) 多巴(二羟基苯丙氨酸)阳性黑素细胞随时间逐渐增加。移植后21至28天的表皮在临床和组织学上似乎形态完整。白细胞介素 - 1(IL - 1)在愈合早期的表皮一些基底细胞中清晰可测,尤其是在黑素细胞和一些角质形成细胞中。转化生长因子 - α(TGF - α)在移植后不久首先在黑素细胞和一些角质形成细胞中在表皮中被检测到,在愈合后期再次被检测到。它也在一些真皮细胞中被发现。其表达与角质形成细胞增殖和黑素细胞迁移一致。TGF - β在移植后第一周后在表皮和真皮中强烈表达。(iv) ICAM - 1仅在愈合开始时短暂表达。我们之前报道过促阿片黑素皮质素及其衍生物MSH/ACTH在人异种移植物愈合过程中强烈表达。本报告所涉及的另外4种分子在愈合的人皮肤中均以可预测的顺序和数量(染色强度)表达。这些数据共同支持了我们的假设,即愈合是一个由多种细胞因子介导的高度调节的过程。