Colić M, Drabek D
Institute of Medical Research, Military Medical Academy, Belgrade, Yugoslavia.
Immunol Lett. 1991 Jun;28(3):251-7. doi: 10.1016/0165-2478(91)90012-y.
The expression of intercellular adhesion molecule 1 (ICAM-1) was studied on freshly isolated rat thymic macrophages (TMF) and after their cultivation in serum-free medium using monoclonal antibody (mAb) 1A 29 and a streptavidin-biotin immunoperoxidase technique. ICAM-1 was expressed on about 80% of freshly isolated TMF. Upon cultivation, the percentage of ICAM-1+ TMF decreased to about 30-40% in 12-day-old culture. Using double immunofluorescence staining it was found that ICAM-1 was expressed both on cortical (R-MC 40+) and CMZ/medullary (R-MC 43+) macrophage subsets. ICAM-1 was up-regulated on TMF in culture by recombinant IFN-gamma, IL1 and TNF-alpha and was down-regulated by dexamethasone. Syngeneic thymocytes bound to cultivated TMF in a rosette form at both 37 degrees C and 4 degrees C. IFN-gamma treatment did not increase the binding formation. The binding between thymocytes and IFN-gamma-stimulated TMF at 37 degrees C was inhibited by pretreatment of TMF with anti-ICAM-1 mAb or pretreatment of thymocytes with anti-LFA-1 mAb, indicating that ICAM-1 on TMF is one of the ligands involved in TMF/thymocyte adhesion and subsequent direct cell-cell communication.
采用单克隆抗体(mAb)1A 29和链霉亲和素-生物素免疫过氧化物酶技术,研究了新鲜分离的大鼠胸腺巨噬细胞(TMF)及其在无血清培养基中培养后的细胞间黏附分子1(ICAM-1)的表达。约80%的新鲜分离的TMF表达ICAM-1。培养后,在12日龄培养物中,ICAM-1+ TMF的百分比降至约30%-40%。通过双重免疫荧光染色发现,ICAM-1在皮质(R-MC 40+)和CMZ/髓质(R-MC 43+)巨噬细胞亚群中均有表达。培养中的TMF上的ICAM-1可被重组IFN-γ、IL-1和TNF-α上调,并被地塞米松下调。同基因胸腺细胞在37℃和4℃时均以玫瑰花结形式与培养的TMF结合。IFN-γ处理并未增加结合形成。用抗ICAM-1 mAb预处理TMF或用抗LFA-1 mAb预处理胸腺细胞可抑制37℃时胸腺细胞与IFN-γ刺激的TMF之间的结合,这表明TMF上的ICAM-1是参与TMF/胸腺细胞黏附及随后直接细胞间通讯的配体之一。