KIT signaling is dispensable for human mast cell progenitor development-Reference-Cited by-同舟云学术

KIT signaling is dispensable for human mast cell progenitor development

Published:2017-10-19 Issue:16 Volume:130 Page:1785-1794
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Dahlin Joakim S.¹,Ekoff Maria¹,Grootens Jennine¹,Löf Liza²,Amini Rose-Marie³,Hagberg Hans³,Ungerstedt Johanna S.⁴⁵,Olsson-Strömberg Ulla⁶⁷,Nilsson Gunnar¹⁶⁷

Affiliation:

1. Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden;

2. Department of Immunology, Genetics and Pathology, Science for Life Laboratory, and

3. Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden;

4. Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden;

5. Hematology Center, Karolinska University Hospital, Stockholm, Sweden;

6. Department of Medical Sciences, Uppsala University, Uppsala, Sweden; and

7. Division of Hematology, Uppsala University Hospital, Uppsala, Sweden

Abstract

Key Points SCF and KIT signaling are dispensable for the survival, proliferation, and maturation of human mast cell progenitors.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/130/16/1785/1403074/blood773374.pdf

Reference53 articles.

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3. Induction of differentiation of human mast cells from bone marrow and peripheral blood mononuclear cells by recombinant human stem cell factor/kit-ligand in long-term culture;Valent;Blood,1992

4. Interleukin 3: a differentiation and growth factor for the mouse mast cell that contains chondroitin sulfate E proteoglycan;Razin;J Immunol,1984

5. Primary structure and functional expression of rat and human stem cell factor DNAs;Martin;Cell,1990

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