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B细胞处理及呈递肽和天然蛋白质抗原的时间依赖性。

Time dependence of B cell processing and presentation of peptide and native protein antigens.

作者信息

Lakey E K, Casten L A, Niebling W L, Margoliash E, Pierce S K

机构信息

Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston IL 60208.

出版信息

J Immunol. 1988 May 15;140(10):3309-14.

PMID:2834435
Abstract

Th cell recognition of globular proteins requires the uptake and intracellular processing of the native Ag by an APC to produce a peptide fragment containing the T cell antigenic determinant, which is recognized in conjunction with Ia. This report describes the time course of the processing and presentation of a soluble globular protein Ag, pigeon cytochrome c (Pc), and of the presentation of a C-terminal peptide fragment of Pc, residues 81 to 104 (Pc 81-104), which does not require processing. Splenic B cells, acting as APC, require 6 to 8 h incubation with native Pc to process and present it to an I-Ek-restricted Pc-specific T cell hybrid, resulting in the secretion of IL-2. Moreover, the time required for B cells to process Pc is the same whether the Ag is taken up by nonspecific fluid phase pinocytosis or by binding to surface Ig. Once processed, Ag is lost from the B cell surface by 8 to 12 h, although when provided with fresh Pc, the same B cells are still capable of processing and presenting. In contrast to native Pc, only 1 to 2 h are required for the peptide fragment Pc 81-104 to become associated with B cells in a stimulatory fashion, and this time is similar for live and paraformaldehyde-fixed B cells, which cannot internalize or process the peptide. Washed free of excess peptide after 2 h, B cells lose their ability to stimulate T cells by 8 to 12 h, with a time course indistinguishable from that for the loss of processed native Pc. Prolonged incubation of B cells with the peptide for 18 to 24 h results in a dramatic loss of the ability to present Pc 81-104. Even when provided with fresh Pc or Pc 81-104, these cells have diminished ability to present these Ag. This loss is selective, inasmuch as these B cells remain equivalent to untreated B cells in the presentation of an unrelated Ag, OVA, to an I-Ak-restricted specific T cell. However, the ability to present another I-Ek-restricted antigenic peptide of the D glycoprotein of HSV to its specific T cell is also diminished. Loss of activity is observed after incubation only with the peptide and not with the native protein and is not due to a depletion of the antigenic peptide from the incubation medium.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

Th细胞对球状蛋白的识别需要抗原呈递细胞(APC)摄取天然抗原并在细胞内进行加工,以产生包含T细胞抗原决定簇的肽片段,该片段与Ia分子结合后被识别。本报告描述了可溶性球状蛋白抗原——鸽细胞色素c(Pc)的加工和呈递的时间进程,以及Pc的C末端肽片段(第81至104位氨基酸残基,Pc 81-104)的呈递情况,该片段不需要加工。作为APC的脾B细胞需要与天然Pc孵育6至8小时,以加工并将其呈递给I-Ek限制的Pc特异性T细胞杂交体,从而导致白细胞介素-2的分泌。此外,无论抗原是通过非特异性液相胞饮作用摄取还是通过与表面免疫球蛋白结合摄取,B细胞加工Pc所需的时间都是相同的。一旦加工完成,抗原在8至12小时内从B细胞表面消失,不过当提供新鲜的Pc时,相同的B细胞仍然能够进行加工和呈递。与天然Pc不同,肽片段Pc 81-104仅需1至2小时就能以刺激的方式与B细胞结合,对于活的和经多聚甲醛固定的B细胞来说,这段时间是相似的,而固定后的B细胞无法内化或加工该肽。在2小时后洗去多余的肽,B细胞在8至12小时后失去刺激T细胞的能力,其时间进程与加工后的天然Pc消失的时间进程无法区分。B细胞与该肽长时间孵育18至24小时会导致呈递Pc 81-104的能力急剧丧失。即使提供新鲜的Pc或Pc 81-104,这些细胞呈递这些抗原的能力也会减弱。这种丧失具有选择性,因为在将无关抗原卵清蛋白(OVA)呈递给I-Ak限制的特异性T细胞时,这些B细胞与未处理的B细胞相当。然而,将单纯疱疹病毒D糖蛋白的另一种I-Ek限制的抗原肽呈递给其特异性T细胞的能力也会减弱。仅在与肽孵育后而非与天然蛋白孵育后观察到活性丧失,且这并非由于孵育培养基中抗原肽的耗尽所致。(摘要截短至400字)

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