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PMID: 9570519 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 160 ·No. 3 ·1998-02-01 ·Pages 1078-84

Kapasi ZF, Qin D, Kerr WG, Kosco-Vilbois MH, Shultz LD, Tew JG, Szakal AK

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.

MeSH Terms
Animals Bone Marrow Transplantation/pathology Crosses, Genetic Dendritic Cells/cytology,immunology,transplantation Female Fetus Lac Operon/immunology Liver Transplantation/pathology Lymphoid Tissue/cytology,immunology,transplantation Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, SCID Rats Rats, Inbred Lew Severe Combined Immunodeficiency/immunology,pathology,therapy Stem Cell Transplantation Stem Cells/cytology,immunology Transfection/immunology
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kapasi Z F
Department of Microbiology and Immunology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298, USA.
Qin D
Kerr W G
Kosco-Vilbois M H
Shultz L D
Tew J G
Szakal A K
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1998-02-01
Pages
1078-84
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIA NIH HHS · AG 05374 · United States
NIAID NIH HHS · AI 17142 · United States
NIAID NIH HHS · AI 30389 · United States
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