Danilenko D M, Ring B D, Lu J Z, Tarpley J E, Chang D, Liu N, Wen D, Pierce G F
Department of Experimental Pathology, Amgen, Inc., Thousand Oaks, California 91320-1789.
J Clin Invest. 1995 Feb;95(2):842-51. doi: 10.1172/JCI117734.
Neu differentiation factor (NDF) is a 44-kD glycoprotein which was isolated from ras-transformed rat fibroblasts and indirectly induces tyrosine phosphorylation of the HER-2/neu receptor via binding to either the HER-3 or HER-4 receptor. NDF contains a receptor binding epidermal growth factor (EGF)-like domain and is a member of the EGF family. There are multiple different isoforms of NDF which arise by alternative splicing of a single gene. To date, in vivo biologic activities have not been demonstrated for any NDF isoform. Since NDF, HER-2/neu, and HER-3 are present in skin, and other EGF family members can influence wound keratinocytes in vivo, we investigated whether NDF would stimulate epidermal migration and proliferation in a rabbit ear model of excisional wound repair. In this model, recombinant human NDF-alpha 2 (rhNDF-alpha 2), applied once at the time of wounding, induced a highly significant increase in both epidermal migration and epidermal thickness at doses ranging from 4 to 40 micrograms/cm2. In contrast, rhNDF-alpha 1, rhNDF-beta 1, and rhNDF-beta 2 had no apparent biologic effects in this model. rhNDF-alpha 2 also induced increased neoepidermal expression of alpha 5 and alpha 6 integrins, two of the earliest integrins to appear during epidermal migration. In addition, rhNDF-alpha 2-treated wounds exhibited increased neoepidermal expression of cytokeratin 10 and filaggrin, both epidermal differentiation markers. NDF alpha isoforms were expressed in dermal fibroblasts of wounded and unwounded skin, while both HER-2/neu and HER-3 were expressed in unwounded epidermis and dermal adnexa. In wounds, HER-2/neu expression was markedly decreased in the wound neoepidermis while neoepidermal HER-3 expression was markedly upregulated. Taken together, these results suggest that endogenous NDF-alpha 2 may function as a paracrine mediator directing initial epidermal migration during cutaneous tissue repair.
神经分化因子(NDF)是一种44-kD糖蛋白,从经ras转化的大鼠成纤维细胞中分离得到,它通过与HER-3或HER-4受体结合间接诱导HER-2/neu受体的酪氨酸磷酸化。NDF含有一个受体结合表皮生长因子(EGF)样结构域,是EGF家族的成员。NDF有多种不同的异构体,由单个基因的可变剪接产生。迄今为止,尚未证明任何NDF异构体具有体内生物学活性。由于NDF、HER-2/neu和HER-3存在于皮肤中,且其他EGF家族成员可在体内影响伤口角质形成细胞,我们研究了NDF是否会在兔耳切除伤口修复模型中刺激表皮迁移和增殖。在该模型中,在伤口形成时一次性应用重组人NDF-α2(rhNDF-α2),在4至40微克/平方厘米的剂量范围内可显著提高表皮迁移和表皮厚度。相比之下,rhNDF-α1、rhNDF-β1和rhNDF-β2在该模型中没有明显的生物学效应。rhNDF-α2还诱导了α5和α6整合素的新表皮表达增加,这是表皮迁移过程中最早出现的两种整合素。此外,经rhNDF-α2处理的伤口显示细胞角蛋白10和丝聚合蛋白的新表皮表达增加,这两种都是表皮分化标志物。NDFα异构体在受伤和未受伤皮肤的真皮成纤维细胞中表达,而HER-2/neu和HER-3在未受伤的表皮和皮肤附属器中表达。在伤口中,HER-2/neu在伤口新表皮中的表达明显降低,而新表皮中HER-3的表达明显上调。综上所述,这些结果表明内源性NDF-α2可能作为旁分泌介质在皮肤组织修复过程中指导初始表皮迁移。