Cited by 268Mast cells and histamineGastrointestinal Tumor Research and Treatmentmelanin and skin pigmentation

Recombinant human stem cell factor (kit ligand) promotes human mast cell and melanocyte hyperplasia and functional activation in vivo

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Costa, J J, Demetri, G D, Harrist, T J, Dvorak, A M, Hayes, D F, Merica, E A, Menchaca, D M, Gringeri, A J +2 more·1996·The Journal of Experimental Medicine

Abstract

Stem cell factor (SCF), also known as mast cell growth factor, kit ligand, and steel factor, is the ligand for the tyrosine kinase receptor (SCFR) that is encoded by the c-kit proto-oncogene. We analyzed the effects of recombinant human SCF (r-hSCF, 5-50 micrograms/kg/day, injected subcutaneously) on mast cells and melanocytes in a phase I study of 10 patients with advanced breast carcinoma. A wheal and flare reaction developed at each r-hSCF injection site; by electron microscopy, most dermal mast cells at these sites exhibited extensive, anaphylactic-type degranulation. A 14-d course of r-hSCF significantly increased dermal mast cell density at sites distant to those injected with the cytokine and also increased both urinary levels of the major histamine metabolite, methyl-histamine, and serum levels of mast cell alpha-tryptase. Five subjects developed areas of persistent hyperpigmentation at r-hSCF injection sites; by light microscopy, these sites exhibited markedly increased epidermal melanization and increased numbers of melanocytes. The demonstration that r-hSCF can promote both the hyperplasia and the functional activation of human mast cells and melanocytes in vivo has implications for our understanding of the role of endogenous SCF in health and disease. These findings also indicate that the interaction between SCF and its receptor represents a potential therapeutic target for regulating the numbers and functional activity of both mast cells and cutaneous melanocytes.

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References 27 · Cited by 268

Authors
Costa, J. J., Demetri, G. D., Harrist, T. J., Dvorak, A. M., Hayes, D. F., Merica, E. A., Menchaca, D. M., Gringeri, A. J., Schwartz, L. B., & Galli, S. J.
Affiliations
  • Harvard University (US)
  • Department of Pathology, Beth Israel Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.
Venue
The Journal of Experimental Medicine
Published
1996-06-01
Volume
183
Issue
6
Pages
2681-2686
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2088310945
Cited by
268
References
27
Citations by year
2026: 6 · 2025: 1 · 2024: 8 · 2023: 5 · 2022: 5 · 2021: 5 · 2020: 5 · 2019: 5 · 2018: 4 · 2017: 5 · 2016: 2 · 2015: 2 · 2014: 4 · 2013: 2 · 2012: 3
FWCI
7.57
Type
journal article
Language
en
Open access
Locations
  • The Journal of Experimental Medicine (publishedVersion)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
  • Amgen
  • Virginia Commonwealth University
  • National Institutes of Health (5r01gm023990-08, 5r01ai031982-03)
  • National Cancer Institute (CA/AI72074)
  • National Institute of Allergy and Infectious Diseases (AI31982, AI/GM23990)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
  • Health Sciences › Medicine › Gastroenterology › Gastrointestinal Tumor Research and Treatment
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
Keywords
stem cell factor, mast cell hyperplasia, mast cell degranulation, wheal and flare, methylhistamine, tryptase, cutaneous hyperpigmentation, breast cancer, CD117, recombinant cytokine therapy, advanced breast cancer
MeSH terms
Proto-Oncogene Mas, Anaphylaxis, Biopsy, Breast Neoplasms, Dose-Response Relationship, Drug, Female, Humans, Hyperplasia, Mast Cells, Melanocytes, Neoplasm Staging, Recombinant Proteins, Skin, Stem Cell Factor

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