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γT细胞抗原受体

The gamma T-cell antigen receptor.

作者信息

Lanier L L, Serafini A T, Ruitenberg J J, Cwirla S, Federspiel N A, Phillips J H, Allison J P, Weiss A

机构信息

Becton Dickinson Monoclonal Center, Inc., Mountain View, California 94043.

出版信息

J Clin Immunol. 1987 Nov;7(6):429-40. doi: 10.1007/BF00915052.

Abstract

The gamma-TCR is encoded by genes composed of V, J, and C elements that demonstrate a limited potential for recombinational diversity. These genes are rearranged, transcribed, and translated into proteins early during thymic ontogeny. Lymphocytes express gamma-TCR proteins on the plasma membrane only in association with the CD3 complex. gamma-TCR glycoproteins usually associate with another non-gamma glycoprotein, designated delta-TCR, to form a heterodimer receptor. Both non-disulfide-bonded and disulfide-bonded gamma/delta-TCR heterodimers have been identified on the plasma membrane of human T lymphocytes. On certain gamma-TCR-bearing T cell lines, a delta-TCR protein cannot be visualized by autoradiography. It is possible that delta-TCR proteins are associated with gamma-TCR glycoproteins on these cell lines but are not efficiently radiolabeled. Alternatively, it has been suggested that homodimers of gamma-TCR proteins can assemble with CD3 and be expressed on the plasma membrane of these cells. In adult lymphoid tissues, the majority of T lymphocytes expresses a CD3, alpha/beta antigen receptor, whereas only a minor subset (less than 5% of peripheral blood lymphocytes, lymph node, spleen, and thymocytes) express a CD3, gamma/delta antigen receptor. IL-2-dependent cell lines of both murine and human CD3, gamma/delta T cells have been established. Most CD3, gamma/delta T cell lines mediate cytotoxicity against a broad spectrum of tumor-cell targets, although the functional significance of this observation remains unclear. Cytotoxicity is apparently not restricted by or directed against MHC antigens. Antibodies against CD3 or gamma-TCR can induce proliferation and IL-2 secretion and can either augment or inhibit cytotoxicity, demonstrating that the gamma/delta-TCR is a functional receptor. The ligand recognized by this receptor has not been identified. The physiological role of T lymphocytes expressing gamma/delta-TCR, the molecular and structural properties of delta-TCR, and the relationship between CD3, alpha/beta T lymphocytes and CD3, gamma/delta T lymphocytes are the major unresolved questions that will be the primary focus of further experimentation.

摘要

γ-TCR 由由 V、J 和 C 元件组成的基因编码,这些基因的重组多样性潜力有限。这些基因在胸腺发育早期进行重排、转录并翻译成蛋白质。淋巴细胞仅在与 CD3 复合物结合时才在质膜上表达 γ-TCR 蛋白。γ-TCR 糖蛋白通常与另一种非γ糖蛋白(称为δ-TCR)结合,形成异二聚体受体。在人 T 淋巴细胞的质膜上已鉴定出非二硫键结合和二硫键结合的γ/δ-TCR 异二聚体。在某些携带γ-TCR 的 T 细胞系上,通过放射自显影无法观察到δ-TCR 蛋白。有可能δ-TCR 蛋白在这些细胞系上与γ-TCR 糖蛋白结合,但未被有效放射性标记。或者,有人提出γ-TCR 蛋白的同二聚体可以与 CD3 组装并在这些细胞的质膜上表达。在成人淋巴组织中,大多数 T 淋巴细胞表达 CD3、α/β抗原受体,而只有一小部分(外周血淋巴细胞、淋巴结、脾脏和胸腺细胞的不到 5%)表达 CD3、γ/δ抗原受体。已经建立了小鼠和人 CD3、γ/δ T 细胞的 IL-2 依赖性细胞系。大多数 CD3、γ/δ T 细胞系介导对多种肿瘤细胞靶标的细胞毒性,尽管这一观察结果的功能意义仍不清楚。细胞毒性显然不受 MHC 抗原的限制或针对 MHC 抗原。抗 CD3 或γ-TCR 的抗体可诱导增殖和 IL-2 分泌,并可增强或抑制细胞毒性,表明γ/δ-TCR 是一种功能性受体。该受体识别的配体尚未确定。表达γ/δ-TCR 的 T 淋巴细胞的生理作用、δ-TCR 的分子和结构特性以及 CD3、α/β T 淋巴细胞与 CD3、γ/δ T 淋巴细胞之间的关系是主要未解决的问题,将是进一步实验的主要重点。

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