首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Antigen processing by epidermal Langerhans cells correlates with the level of biosynthesis of major histocompatibility complex class II molecules and expression of invariant chain
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Antigen processing by epidermal Langerhans cells correlates with the level of biosynthesis of major histocompatibility complex class II molecules and expression of invariant chain

机译:表皮朗格汉斯细胞的抗原加工与主要组织相容性复合物II类分子的生物合成水平和恒定链的表达有关

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摘要

Two prior studies with a small number of T cell lines have shown that the presentation of native protein antigens by epidermal Langerhans cells (LC) is regulated. When freshly isolated, LC are efficient antigen-presenting cells (APC), but after a period of culture LC are inefficient or even inactive. The deficit in culture seems to be a selective loss in antigen processing, since cultured LC are otherwise rich in major histocompatibility complex (MHC) class II products and are active APC for alloantigens and mitogens, which do not require processing. We have extended the analysis by studying presentation to bulk populations of primed lymph node and a T-T hybrid. Only freshly isolated LC can be pulsed with the protein antigens myoglobin and conalbumin, but once pulsed, antigen is retained in an immunogenic form for at least 2 d. The acquisition of antigen, presumably as MHC-peptide complexes, is inhibited if the fresh LC are exposed to foreign protein in the presence of chloroquine or cycloheximide. The latter, in contrast, improves the efficacy of antigen pulsing in anti-Ig- stimulated B blasts. In additional studies of mechanism, we noted that both fresh and cultured LC endocytose similar amounts of an antigen, rhodamineovalbumin, into perinuclear granules. However, freshly isolated LC synthesize high levels class II MHC molecules and express higher amounts of the class II-associated invariant chain. Fresh LC are at least 5-10 times more active than many other cells types in the level of biosynthesis of MHC class II products. These findings provide a physiologic model in which newly synthesized MHC class II molecules appear to be the principal vehicle for effective antigen processing by APC of the dendritic cell lineage. Another APC, the B lymphoblast, does not appear to require newly synthesized MHC class II molecules for presentation.
机译:先前有少量T细胞系的两项研究表明,表皮朗格汉斯细胞(LC)对天然蛋白质抗原的呈递受到调节。当新鲜分离时,LC是有效的抗原呈递细胞(APC),但是经过一段时间的培养,LC效率很低甚至没有活性。培养中的缺陷似乎是抗原加工中的选择性损失,因为培养的LC否则富含主要的组织相容性复合物(MHC)II类产品,并且对不需要加工的同种抗原和促分裂原具有活性APC。我们通过研究表现形式将分析扩展到大量的致敏淋巴结和T-T杂种人群。只有新鲜分离的LC可以用蛋白抗原肌红蛋白和伴白蛋白进行脉冲处理,但是一旦被脉冲处理,抗原将以免疫原性形式保留至少2 d。如果新鲜的LC在氯喹或环己酰亚胺的存在下暴露于外源蛋白质,则可能会抑制抗原(大概是MHC-肽复合物)的获得。相反,后者在抗Ig刺激的B母细胞中提高了抗原脉冲的功效。在机制的其他研究中,我们注意到新鲜和培养的LC胞吞酶将相似量的抗原如罗丹明卵白蛋白带入核周颗粒中。但是,新鲜分离的LC合成了高水平的II类MHC分子,并表达了大量的II类相关不变链。在MHC II类产品的生物合成水平上,新鲜LC的活性至少是许多其他细胞类型的5-10倍。这些发现提供了一种生理模型,其中新合成的II类MHC分子似乎是通过树突状细胞谱系的APC有效进行抗原加工的主要载体。另一种APC B淋巴母细胞似乎不需要新合成的II类MHC分子来表达。

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