Nanney L B, Ellis D L, Levine J, King L E
Department of Plastic Surgery, Vanderbilt University, Nashville, TN 37232.
Am J Pathol. 1992 Apr;140(4):915-25.
The altered distribution of epidermal growth factor receptors (EGF-R) in hyperproliferative skin lesions such as psoriasis vulgaris, seborrheic keratoses, acanthosis nigricans, ichthyosis, and others implies aberrant control of growth/proliferation by epidermal growth factor (EGF), transforming growth factor alpha (TGF alpha), and other growth factors/cytokines. Whether overexpression of EGF-R: 1) correlates with epidermal proliferation, 2) serves as a hallmark of specific dermatoses, or 3) is due to modulation by multiple growth factors remains unclear. To correlate distributions of EGF-R with in vivo proliferative status, two benign diseases of unknown etiology, seborrheic keratoses and acrochordons (skin tags), were examined using EGF-R immunolocalization and 125I-EGF binding techniques. Lesions documented as growing by clinical criteria or 5-bromodeoxyuridine incorporation (a measure of cell proliferation) were compared to nongrowing lesions of the same type. To correlate distributions of EGF-R to specific dermatoses, skin diseases of viral etiology (verruca vulgaris and molluscum contagiosum) were also probed by EGF-R immunolocalization and 125I-EGF binding. Elevated immunostaining for EGF-R and 125I-EGF binding sites were associated with actively growing seborrheic keratoses and skin tags whereas normal patterns of immunostaining and 125I-EGF binding were seen in nongrowing seborrheic keratoses and skin tags. Viral diseases showed unique patterns. No EGF-R were detected in verruca vulgaris. Molluscum contagiosum lesions showed intense EGF-R in basal keratinocytes and no EGF-R in virally infected cells. Thus elevations in EGF-R show a positive in vivo correlation with proliferation in at least two differing benign diseases of the epidermis. The decreased levels of EGF-R in virally infected lesions suggests that EGF-R may show unique patterns for specific dermatoses and are not universally elevated in benign hyperproliferative skin disorders.
在寻常型银屑病、脂溢性角化病、黑棘皮病、鱼鳞病等增生性皮肤病变中,表皮生长因子受体(EGF-R)分布的改变意味着表皮生长因子(EGF)、转化生长因子α(TGFα)以及其他生长因子/细胞因子对生长/增殖的调控异常。EGF-R的过表达是否:1)与表皮增殖相关,2)作为特定皮肤病的标志,或3)由多种生长因子调节,仍不清楚。为了将EGF-R的分布与体内增殖状态相关联,使用EGF-R免疫定位和125I-EGF结合技术检查了两种病因不明的良性疾病,脂溢性角化病和皮赘。将根据临床标准或5-溴脱氧尿苷掺入(细胞增殖的一种测量方法)记录为生长的病变与相同类型的非生长病变进行比较。为了将EGF-R的分布与特定皮肤病相关联,还通过EGF-R免疫定位和125I-EGF结合对病毒病因的皮肤病(寻常疣和传染性软疣)进行了检测。EGF-R免疫染色和125I-EGF结合位点升高与活跃生长的脂溢性角化病和皮赘相关,而在非生长的脂溢性角化病和皮赘中观察到正常的免疫染色和125I-EGF结合模式。病毒性疾病表现出独特的模式。寻常疣中未检测到EGF-R。传染性软疣病变在基底角质形成细胞中显示强烈的EGF-R,而在病毒感染细胞中未检测到EGF-R。因此,EGF-R的升高在体内与至少两种不同的表皮良性疾病中的增殖呈正相关。病毒感染病变中EGF-R水平的降低表明,EGF-R可能显示特定皮肤病的独特模式,并且在良性增生性皮肤疾病中并非普遍升高。