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从人十二指肠黏膜产生的CD56+ CD16- CD3-大颗粒淋巴细胞纯群体的形态学、表型和功能特征

Morphological, phenotypic and functional characteristics of a pure population of CD56+ CD16- CD3- large granular lymphocytes generated from human duodenal mucosa.

作者信息

Pang G, Buret A, Batey R T, Chen Q Y, Couch L, Cripps A, Clancy R

机构信息

Department of Pathology, Faculty of Medicine, University of Newcastle, New South Wales, Australia.

出版信息

Immunology. 1993 Jul;79(3):498-505.

Abstract

Interleukin-2 (IL-2)-dependent large granular lymphocytes (LGL) with a distinctive surface phenotype were generated from histologically normal duodenal biopsy tissues. Immunoperoxidase staining of the mucosa with an anti-CD56 monoclonal antibody revealed LGL localized in the lamina propria rather than in the epithelium. Light and electron microscopy demonstrated azurophilic and electron-dense cytoplasmic granules. Flow cytometry analysis revealed that these cells express CD45, CD56, CD2, CD7, CD11a, CD18, CD69 and the intermediate affinity (p70) IL-2 receptor (IL-2R) but not CD57, CD16, CD3, CD4, CD5, CD8, CD45RA, CD25, or the high affinity p55 IL-2R. The LGL proliferated when cultured in the presence of human rIL-2 but not in the presence of human rIL-4. Functional studies demonstrated that the LGL had strong cytotoxicity against natural killer (NK) target cells, K562, but not NK-resistant targets such as Colo 205, Melanoma and Epstein-Barr virus (EBV)-transformed B-cell lines. The LGL expressed genes for IL-5, IL-8, granulocyte-macrophage colony-stimulating factor (GM-CSF) and tumour necrosis factor-alpha (TNF-alpha) and the corresponding cytokines were detected in culture supernatant. These results provide evidence for an important role of gut mucosal LGL in the induction and regulation of inflammation and immunity in the gut.

摘要

从组织学正常的十二指肠活检组织中产生了具有独特表面表型的白细胞介素-2(IL-2)依赖性大颗粒淋巴细胞(LGL)。用抗CD56单克隆抗体对黏膜进行免疫过氧化物酶染色显示,LGL定位于固有层而非上皮层。光镜和电镜检查显示有嗜天青和电子致密的胞质颗粒。流式细胞术分析表明,这些细胞表达CD45、CD56、CD2、CD7、CD11a、CD18、CD69和中等亲和力(p70)的IL-2受体(IL-2R),但不表达CD57、CD16、CD3、CD4、CD5、CD8、CD45RA、CD25或高亲和力的p55 IL-2R。LGL在人重组IL-2存在的情况下培养时会增殖,但在人重组IL-4存在的情况下不会增殖。功能研究表明,LGL对自然杀伤(NK)靶细胞K562具有强大的细胞毒性,但对NK抗性靶细胞如Colo 205、黑色素瘤和爱泼斯坦-巴尔病毒(EBV)转化的B细胞系则没有细胞毒性。LGL表达IL-5、IL-8、粒细胞-巨噬细胞集落刺激因子(GM-CSF)和肿瘤坏死因子-α(TNF-α)的基因,并且在培养上清液中检测到了相应的细胞因子。这些结果为肠道黏膜LGL在肠道炎症和免疫的诱导及调节中的重要作用提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc6/1421995/c326c13745b7/immunology00094-0163-a.jpg

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