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原发性淋巴组织中的滤泡树突状细胞(FDC)前体细胞。

Follicular dendritic cell (FDC) precursors in primary lymphoid tissues.

作者信息

Kapasi Z F, Qin D, Kerr W G, Kosco-Vilbois M H, Shultz L D, Tew J G, Szakal A K

机构信息

Department of Microbiology and Immunology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298, USA.

出版信息

J Immunol. 1998 Feb 1;160(3):1078-84.

PMID:9570519
Abstract

The origin of follicular dendritic cells (FDC) is unresolved, and as such, remains controversial. Based on the migration of Ag-transporting cells (ATC) into lymphoid follicles and the phenotypic similarity between FDC and ATC, one hypothesis is that ATC may represent emigrating FDC precursors. This contrasts with the view that FDC originate from local stromal cells in the secondary lymphoid tissues. Mice homozygous for the severe combined immunodeficiency (prkdc(scid)) mutation (scid) lack FDC. Thus, they provide a powerful tool for assessing de novo generation of FDC. To test whether FDC precursors could be found in bone marrow or fetal liver, scid/scid mice were reconstituted with either: 1) bone marrow cells from (BALB/c x C57BL/6)F1 donors, 2) bone marrow cells from ROSA BL/6 F1 (lacZ-transfected) mice, 3) rat bone marrow cells, or 4) rat fetal liver cells. Six to eight weeks after reconstitution with F1 bone marrow, cells reactive with the FDC-labeling mAb, FDC-M1, also expressed donor class I molecules on their surfaces. Similarly in mice reconstituted with lacZ-transfected bone marrow cells, these cells were also positive for the lacZ gene product. Furthermore, in spleens of animals reconstituted with either rat bone marrow or rat fetal liver, rat FDC were identified using the specifically labeling mAb, ED5. In all cases, host FDC were also present, indicating that scid/scid mice have FDC precursors that will mature in the presence of allogeneic or xenogeneic lymphoid cells. In summary, FDC can be derived from progenitor cells present in primary lymphoid tissues.

摘要

滤泡树突状细胞(FDC)的起源尚未明确,因此仍存在争议。基于抗原转运细胞(ATC)向淋巴滤泡的迁移以及FDC与ATC之间的表型相似性,一种假说是ATC可能代表迁出的FDC前体。这与FDC起源于次级淋巴组织中的局部基质细胞的观点形成对比。严重联合免疫缺陷(prkdc(scid))突变(scid)的纯合小鼠缺乏FDC。因此,它们为评估FDC的从头生成提供了一个强大的工具。为了测试是否能在骨髓或胎肝中找到FDC前体,scid/scid小鼠用以下细胞进行重建:1)来自(BALB/c×C57BL/6)F1供体的骨髓细胞,2)来自ROSA BL/6 F1(lacZ转染)小鼠的骨髓细胞,3)大鼠骨髓细胞,或4)大鼠胎肝细胞。用F1骨髓重建后6至8周,与FDC标记单克隆抗体FDC-M1反应的细胞在其表面也表达供体I类分子。同样,在用lacZ转染的骨髓细胞重建的小鼠中,这些细胞对lacZ基因产物也呈阳性。此外,在用大鼠骨髓或大鼠胎肝重建的动物脾脏中,使用特异性标记单克隆抗体ED5鉴定出大鼠FDC。在所有情况下,宿主FDC也存在,表明scid/scid小鼠具有FDC前体,这些前体在同种异体或异种淋巴细胞存在的情况下会成熟。总之,FDC可源自初级淋巴组织中存在的祖细胞。

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