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腹膜腔B细胞的Mls呈递

Mls presentation by peritoneal cavity B cells.

作者信息

Riggs James E, Howell Koko F, Taylor Justin, Mahjied Tazee, Prokopenko Nataliya, Alvarez John, Coleman Clenton

机构信息

Department of Biology, Rider University, 2083 Lawrenceville Road, Lawrenceville, NJ 08648-3099, USA.

出版信息

Immunobiology. 2004;209(3):255-64. doi: 10.1016/j.imbio.2004.03.008.

Abstract

DBA/2J spleen and peritoneal cells were compared for their ability to present the minor lymphocyte stimulatory superantigen Mls-1a. Although capable of Mls presentation in vivo, peritoneal cells were less effective than spleen cells in vitro. This difference was not due to cell concentration or culture duration. Flow cytometric comparison of spleen and peritoneal B cells revealed no significant differences in cell surface markers needed for cognate interaction with T cells. Resolution of peritoneal B cell subsets by cell sorting revealed that even though B-1 cells were capable of Mls presentation, they were less effective than B-2 cells. Mixing experiments showed that B-1 cells did not inhibit B-2 cell presentation of Mls. In contrast, total peritoneal cells inhibited T cell responses to Mls presented by spleen cells. The peritoneal cavity harbors B cells that can present Mls as well as other cells that can suppress this response.

摘要

比较了DBA/2J小鼠的脾细胞和腹腔细胞呈递次要淋巴细胞刺激超抗原Mls-1a的能力。虽然腹腔细胞在体内能够呈递Mls,但在体外其效果不如脾细胞。这种差异并非由于细胞浓度或培养时间。对脾细胞和腹腔B细胞进行流式细胞术比较,结果显示与T细胞进行同源相互作用所需的细胞表面标志物并无显著差异。通过细胞分选对腹腔B细胞亚群进行分析,结果表明,尽管B-1细胞能够呈递Mls,但其效果不如B-2细胞。混合实验表明,B-1细胞不会抑制B-2细胞呈递Mls。相反,总的腹腔细胞会抑制T细胞对脾细胞呈递的Mls的反应。腹腔中存在能够呈递Mls的B细胞以及能够抑制这种反应的其他细胞。

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