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黑色素瘤和黑素细胞的表面抗原。人γ干扰素诱导Ia抗原的特异性。

Surface antigens of melanoma and melanocytes. Specificity of induction of Ia antigens by human gamma-interferon.

作者信息

Houghton A N, Thomson T M, Gross D, Oettgen H F, Old L J

出版信息

J Exp Med. 1984 Jul 1;160(1):255-69. doi: 10.1084/jem.160.1.255.

Abstract

IFN-gamma is known to induce expression of Ia antigens on a variety of cell types. In the present study, this activity of IFN-gamma has been analyzed with a panel of 36 melanoma cell lines, normal melanocytes, and 97 cell lines representing a range of other differentiation lineages. 55% of the melanoma cell lines express Ia antigens in a constitutive manner without IFN-gamma induction. Of the 16 Ia-melanoma lines, 13 could be induced to express Ia antigens by IFN-gamma, whereas three were noninducible. Melanocytes, which do not normally express Ia antigens, are converted to Ia expression by IFN-gamma. Ia antigens expressed constitutively or after IFN-gamma induction were identified with antibodies detecting monomorphic and allomorphic products of DR and DC loci. IFN-gamma appeared to be unique in its ability to induce Ia expression on melanoma and melanocytes; 14 other agents (including IFN-alpha and IFN-beta) known to influence growth or differentiation did not have Ia-inducing activity. Equally striking is the restriction of antigenic changes following IFN-gamma induction to HLA-associated products; of the 38 systems of cell surface antigens examined, only HLA-A,B,C, beta 2m, and Ia antigens were affected. A variety of other Ia- cell types were shown to be Ia-inducible by IFN-gamma; these included established lines of breast, colon, pancreas, bladder, kidney, ovary, and brain cancers, and cultures of normal fibroblasts, kidney epithelia, and epidermal keratinocytes. In contrast, three tumor types, teratocarcinoma, choriocarcinoma, and neuroblastoma, were not inducible for Ia expression, even though IFN-gamma could induce expression of HLA-A,B,C products. The broad representation of Ia antigens on most somatic cell types expressed either constitutively or after IFN-gamma can be viewed in an immunological context (antigen presentation/immune regulatory signals) or could indicate that Ia products have functions other than those related to immune reactions.

摘要

已知γ干扰素可诱导多种细胞类型表达Ia抗原。在本研究中,使用一组包含36个黑色素瘤细胞系、正常黑素细胞以及代表一系列其他分化谱系的97个细胞系,对γ干扰素的这一活性进行了分析。55%的黑色素瘤细胞系以组成型方式表达Ia抗原,无需γ干扰素诱导。在16个Ia阳性黑色素瘤细胞系中,13个可被γ干扰素诱导表达Ia抗原,而3个不可诱导。通常不表达Ia抗原的黑素细胞经γ干扰素作用后可转变为Ia阳性表达。通过检测DR和DC位点单态性及同种异型产物的抗体,可鉴定组成型表达或γ干扰素诱导后表达的Ia抗原。γ干扰素在诱导黑色素瘤细胞和黑素细胞表达Ia抗原方面似乎具有独特性;已知的其他14种影响生长或分化的因子(包括α干扰素和β干扰素)均无Ia诱导活性。同样引人注目的是,γ干扰素诱导后抗原变化仅限于与HLA相关的产物;在所检测的38种细胞表面抗原系统中,仅HLA - A、B、C、β2m和Ia抗原受到影响。多种其他Ia阴性细胞类型经γ干扰素作用后显示可诱导表达Ia抗原;这些细胞包括乳腺癌、结肠癌、胰腺癌、膀胱癌、肾癌、卵巢癌和脑癌的 established lines,以及正常成纤维细胞、肾上皮细胞和表皮角质形成细胞培养物。相比之下,三种肿瘤类型,即畸胎癌、绒毛膜癌和神经母细胞瘤,即使γ干扰素可诱导HLA - A、B、C产物表达,也不能诱导Ia表达。在免疫背景(抗原呈递/免疫调节信号)下,可以看到大多数体细胞类型中组成型表达或γ干扰素作用后表达的Ia抗原具有广泛代表性,或者这可能表明Ia产物具有除与免疫反应相关功能之外的其他功能。

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