Suppr超能文献

肾移植血管内单核细胞中表皮脂肪酸结合蛋白的诱导

Induction of epidermal fatty acid binding protein in intravascular monocytes of renal allografts.

作者信息

Grau Veronika, Garn Holger, Bette Michael, Spener Friedrich, Steiniger Birte, Gemsa Diethard, Stehling Oliver

机构信息

Institute of Anatomy and Cell Biology, Philipps University, Marburg, Germany.

出版信息

Transplantation. 2003 Mar 15;75(5):685-8. doi: 10.1097/01.TP.0000052591.91653.52.

Abstract

During acute rejection of rat renal allografts, numerous activated monocytes accumulate in the vasculature of the graft. These monocytes seem to be involved in allograft destruction. Proinflammatory and effector functions of monocytes and macrophages can be down-regulated by peroxisome proliferators, which are probably transported in the cytoplasm by fatty acid binding proteins (FABPs). We performed renal transplantation in rats in the Dark Agouti-to-Lewis strain combination. Intravascular graft leukocytes were harvested 4 days posttransplantation. Epidermal (E)-FABP mRNA and protein expression were investigated by reverse-transcriptase polymerase chain reaction and immunoblotting, respectively. E-FABP-expressing cells were identified by immunofluorescence. After allogeneic transplantation, intravascular graft leukocytes expressed E-FABP mRNA and protein. In isografts, significantly lower expression levels were observed. E-FABP protein was detected in monocytes expressing ED1 and in alphabeta-T-cell receptor positive T lymphocytes. E-FABP might regulate monocyte activation and may represent a promising target for a therapeutic intervention in allograft rejection.

摘要

在大鼠肾移植急性排斥反应期间,大量活化的单核细胞积聚在移植肾的血管系统中。这些单核细胞似乎参与了移植肾的破坏。单核细胞和巨噬细胞的促炎及效应功能可被过氧化物酶体增殖剂下调,过氧化物酶体增殖剂可能由脂肪酸结合蛋白(FABP)转运至细胞质中。我们采用暗褐鼠到刘易斯大鼠品系组合进行肾移植。在移植后4天收集移植肾血管内白细胞。分别通过逆转录聚合酶链反应和免疫印迹法研究表皮(E)-FABP mRNA和蛋白表达。通过免疫荧光鉴定表达E-FABP的细胞。同种异体移植后,移植肾血管内白细胞表达E-FABP mRNA和蛋白。在同基因移植中,观察到表达水平显著降低。在表达ED1的单核细胞和αβ-T细胞受体阳性T淋巴细胞中检测到E-FABP蛋白。E-FABP可能调节单核细胞活化,可能是移植排斥治疗干预的一个有前景的靶点。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验