Home LiteratureArticle Details
PMID: 1374104 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Expression of c-kit by mesenteric lymph node cells from Nippostrongylus brasiliensis-infected mice and by mast cell colonies developing from these cells in response to 3T3 fibroblast-conditioned medium.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 148 ·No. 9 ·1992-05-01 ·Pages 2894-8

Leftwich JA, Westin EH, Huff TF

Abstract

Mast cell committed progenitors are nongranulated cells found in mesenteric lymph nodes of mice infected with Nippostrongylus brasiliensis (Nb-MLN) but not from normal mice. Mast cell committed progenitors can respond to either IL-3 or to a factor(s) present in 3T3 fibroblast conditioned media (F-CM) by formation of mast cell colonies. Previous studies from ours and other laboratories suggested that mast cell differentiation involved the W allele product, c-kit, as a receptor and Sl allele product, stem cell factor, as a growth factor. We report here that Nb-MLN cells, which can respond to F-CM by mast cell colony formation, also contain cells that express message for c-kit, and that c-kit message cannot be detected in naive mesenteric lymph node cells, which cannot respond to F-CM. Antisense oligonucleotides to c-kit inhibit mast cell colony formation by Nb-MLN cells in response to F-CM, but not to conditioned medium of PWM-stimulated spleen cells as a source of IL-3. The antisense oligonucleotides also inhibit the degree of granulation by mast cells derived from culture. The results suggest that c-kit and its ligand, stem cell factor, are necessary for mast cell-committed progenitors to proliferate and granulate in response to F-CM but not IL-3.

Related Genes
kit
MeSH Terms
Animals Base Sequence Blotting, Northern Cell Differentiation/physiology Cell Division/physiology Cells, Cultured Female Hematopoietic Cell Growth Factors/biosynthesis Interleukin-3/pharmacology Lymph Nodes/metabolism Mast Cells/physiology Mice Mice, Inbred BALB C Molecular Sequence Data Nematode Infections/metabolism Nippostrongylus Oligonucleotides, Antisense/genetics,pharmacology Polymerase Chain Reaction Proto-Oncogene Proteins/biosynthesis Proto-Oncogene Proteins c-kit RNA/analysis Stem Cell Factor
Chemicals
Hematopoietic Cell Growth Factors Interleukin-3 Oligonucleotides, Antisense Proto-Oncogene Proteins Stem Cell Factor RNA Proto-Oncogene Proteins c-kit
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Leftwich J A
Department of Microbiology and Immunology, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond 23298.
Westin E H
Huff T F
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1992-05-01
Pages
2894-8
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · K04 AI00948 · United States
NIAID NIH HHS · P50 AI28532 · United States
NIAID NIH HHS · R01 AI-25537 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com