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绵羊鼻咽和口咽相关淋巴组织中M细胞标志物的鉴定与特征分析。

Identification and characterization of an M cell marker in nasopharynx- and oropharynx-associated lymphoid tissue of sheep.

作者信息

Saxena Vijay Kumar, Diaz Alejandra, Scheerlinck Jean-Pierre Y

机构信息

Centre for Animal Biotechnology, Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Victoria, 3010, Australia; Division of Animal Physiology and Biochemistry, ICAR-Central Sheep and Wool Research Institute, Avikanagar, Tonk, Rajasthan, 304501, India.

Centre for Animal Biotechnology, Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Victoria, 3010, Australia; Laboratorio de Inmunología, Departamento SAMP, Centro de Investigación Veterinaria de Tandil (CIVETAN-CONICET), Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Pcia. de Bs. As., Tandil, 7000, Buenos Aires, Argentina.

出版信息

Vet Immunol Immunopathol. 2019 Feb;208:1-5. doi: 10.1016/j.vetimm.2018.12.005. Epub 2018 Dec 18.

Abstract

M cells play a pivotal role in the induction of immune responses within the mucosa-associated lymphoid tissues. M cells exist principally in the follicle-associated epithelium (FAE) of the isolated solitary lymphoid follicles as well as in the lymphoid follicles of nasopharynx-associated lymphoid tissue and gut associated lymphoid tissue (GALT). Through lymphatic cannulation it is possible to investigate local immune responses induced following nasal Ag delivery in sheep. Hence, identifying sheep M cell markers would allow the targeting of M cells to offset the problem of trans-epithelial Ag delivery associated with inducing mucosal immunity. Sheep cDNA from the tonsils of the oropharynx and nasopharynx was PCR amplified using Glycoprotein-2 (GP)-specific primers and expressed as a poly-His-tagged recombinant sheep GP (56 kDa) in HEK293 cells. The recombinant GP protein was purified using Ni-NTA affinity chromatography and polyclonal serum against the protein was raised in rats. The antiserum recognized the recombinant sheep GP and purified rat IgG against GP stained M cells in sections of sheep tonsils from nasopharynx and oropharynx. M cells were found to be present in epithelium of the palatine tonsils (oropharynx), pharyngeal tonsils as well as tubal tonsils (nasopharynx). They were also present in the FAE of the scattered lymphoid follicles over the base of the nasopharynx. Thus, GP has been identified to be an important M cell marker of nasopharynx and oropharynx-associated lymphoid tissues in sheep.

摘要

M细胞在黏膜相关淋巴组织内免疫反应的诱导中起关键作用。M细胞主要存在于孤立的单个淋巴滤泡的滤泡相关上皮(FAE)中,以及鼻咽相关淋巴组织和肠道相关淋巴组织(GALT)的淋巴滤泡中。通过淋巴管插管,可以研究绵羊经鼻腔给予抗原后诱导的局部免疫反应。因此,鉴定绵羊M细胞标志物将有助于靶向M细胞,以解决与诱导黏膜免疫相关的跨上皮抗原递送问题。使用糖蛋白-2(GP)特异性引物对来自口咽和鼻咽扁桃体的绵羊cDNA进行PCR扩增,并在HEK293细胞中表达为多组氨酸标签的重组绵羊GP(56 kDa)。使用镍-氮三乙酸亲和层析法纯化重组GP蛋白,并在大鼠中制备针对该蛋白的多克隆血清。抗血清识别重组绵羊GP,针对GP纯化的大鼠IgG对来自鼻咽和口咽的绵羊扁桃体切片中的M细胞进行染色。发现M细胞存在于腭扁桃体(口咽)、咽扁桃体以及咽鼓管扁桃体(鼻咽)的上皮中。它们也存在于鼻咽底部散在淋巴滤泡的FAE中。因此,已确定GP是绵羊鼻咽和口咽相关淋巴组织的重要M细胞标志物。

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