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人淋巴样细胞系的同种抗原;“人Ia样抗原”。通过放射免疫测定法确定的同种抗原活性以及细胞系、器官和组织分布。

Alloantigens of human lymphoid cell lines; 'human Ia-like antigens'. Alloantigenic activity and cell line, organ and tissue distribution as determined by radioimmunoassay.

作者信息

Koyama K, Nakamuro K, Tanigaki N, Pressman D

出版信息

Immunology. 1977 Aug;33(2):217-30.

Abstract

Membrane glycoproteins that appear to belong to a new alloantigen system were partially purified by gel filtration and lentil-lectin affinity chromatography from a non-ionic detergent (Renex 30) solubilized membrane fraction of each of two Burkitt lymphoma cell lines, B46M and Daudi. The preparations were radioiodinated and further purified by gel filtration, lentil—lectin affinity chromatography and anti-HLA antibody affinity chromatography. The labelled preparations thus obtained did not have binding activity with any of rabbit anti-HLA, rabbit anti-human β-microglobulin and rabbit anti-human IgG-Fab antisera, but did have a high level of binding activity with rabbit anti-B-cell membrane antiserum. Moreover, the labelled preparations showed relatively high binding activity with some conventional HLA typing sera. Out of sixty-eight human tissue typing alloantisera tested, three (Berlin 373, Betz and TO-29-01) gave especially high binding with both of the labeled preparations. The antigens involved in reaction with these alloantisera and also with the rabbit anti-B-cell membrane antiserum contained two components, one 31,000 ∼ 32,000 daltons and another 24,000 ∼ 25,000 daltons, bound non-covalently. The alloantigens were specific to B cell type cell lines (B-lymphoid cell lines and Burkitt-lymphoma cell lines) in cultured cell lines and also to B lymphocytes in peripheral blood. In organs and tissues, however, they were found to be present widely distributed in lymphoid organs (thymus as well as spleen and lymph node) and in non-lymphoid organs (including liver, kidney, testis and heart).

摘要

从两种伯基特淋巴瘤细胞系B46M和Daudi的非离子去污剂(Renex 30)溶解的膜组分中,通过凝胶过滤和扁豆凝集素亲和层析对似乎属于一种新的同种抗原系统的膜糖蛋白进行了部分纯化。将制备物进行放射性碘化,然后通过凝胶过滤、扁豆凝集素亲和层析和抗HLA抗体亲和层析进一步纯化。由此获得的标记制备物与兔抗HLA、兔抗人β-微球蛋白和兔抗人IgG-Fab抗血清均无结合活性,但与兔抗B细胞膜抗血清具有高水平的结合活性。此外,标记制备物与一些传统的HLA分型血清显示出相对较高的结合活性。在测试的68种人体组织分型同种抗血清中,有三种(柏林373、贝茨和TO-29-01)与两种标记制备物的结合特别高。与这些同种抗血清以及兔抗B细胞膜抗血清反应所涉及的抗原包含两个组分,一个为31,000~32,000道尔顿,另一个为24,000~25,000道尔顿,它们以非共价方式结合。这些同种抗原在培养细胞系中对B细胞类型的细胞系(B淋巴细胞系和伯基特淋巴瘤细胞系)具有特异性,对外周血中的B淋巴细胞也具有特异性。然而,在器官和组织中,发现它们广泛分布于淋巴器官(胸腺以及脾脏和淋巴结)和非淋巴器官(包括肝脏、肾脏、睾丸和心脏)。

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