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猿猴病毒40转化的人角质形成细胞中SSA/Ro抗原的表达

SSA/Ro antigen expression in simian virus 40-transformed human keratinocytes.

作者信息

Miyagawa S, Okada N, Inagaki Y, Kitano Y, Ueki H, Sakamoto K, Steinberg M L

机构信息

Department of Dermatology, Nara Medical University, Japan.

出版信息

J Invest Dermatol. 1988 Mar;90(3):342-5. doi: 10.1111/1523-1747.ep12456308.

Abstract

SSA/Ro antigen is a soluble cellular component to which antibodies are frequently produced in patients with Sjögren's syndrome and systemic lupus erythematosus. Its exact location within the cell has yet to be determined. In this study we report the expression of SSA/Ro antigen in simian virus 40 (SV40)-transformed keratinocytes. The locations of SSA/Ro, U1RNP, and DNA antigens were studied by indirect immunofluorescence using monospecific antibodies. SSA/Ro antigen was detected in both the nucleus and cytoplasm of SV40-transformed keratinocytes tested with three monospecific sera. Primary cultured keratinocytes derived from adult human skin showed localized immunofluorescent staining within the nucleus. When Ca++ concentration of the medium was switched to 0.05 mM, these cells expressed cytoplasmic SSA/Ro antigens within 48 h. Depletion of the antibody activity with insolubilized human spleen extract abolished the staining. Surface expression of this antigen could not be detected in either primary or transformed cells. Localization of U1RNP and DNA was not altered. These results indicate that expression of SSA/Ro antigen in human keratinocytes is modulated by SV40 infection and that this antigen is expressed to a greater degree in cells that are less differentiated, transformed, or proliferating.

摘要

SSA/Ro抗原是一种可溶性细胞成分,干燥综合征和系统性红斑狼疮患者体内常产生针对它的抗体。其在细胞内的确切位置尚未确定。在本研究中,我们报告了SSA/Ro抗原在猴病毒40(SV40)转化的角质形成细胞中的表达情况。使用单特异性抗体通过间接免疫荧光法研究了SSA/Ro、U1RNP和DNA抗原的定位。用三种单特异性血清检测时,在SV40转化的角质形成细胞的细胞核和细胞质中均检测到了SSA/Ro抗原。源自成人皮肤的原代培养角质形成细胞在细胞核内显示出局部免疫荧光染色。当培养基中的钙离子浓度切换到0.05 mM时,这些细胞在48小时内表达细胞质SSA/Ro抗原。用人脾脏提取物固定化耗尽抗体活性后,染色消失。在原代细胞或转化细胞中均未检测到该抗原的表面表达。U1RNP和DNA的定位未改变。这些结果表明,人角质形成细胞中SSA/Ro抗原的表达受SV40感染调节,且该抗原在分化程度较低、转化或增殖的细胞中表达程度更高。

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