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Published August 1995 | public
Journal Article

Tissue-regulated differentiation and maturation of a v-abl-immortalized mast cell-committed progenitor

Abstract

An immature v-abl-transformed mast cell line (V3-MC) was derived from a mouse that developed systemic mastocytosis after transplantation of v-sbl-infected bone marrow cells. V3-MCs injected intravenously into adult BALE/c mice infiltrated the liver, spleen, and intestine by day 6 and underwent progressive differentiation and maturation, eventually resembling indigenous mast cells. In terms of their protease content, the V3-MCs that localized in the liver and spleen differed from those in the intestine, and both differed from the cultured V3-MCs. The acquired expression of certain proteases and the loss of expression of other proteases in these tissue V3-MCs defines particular phenotypes and Indicates that the differentiation and maturation of mast cell-committed progenitor cells are primarily regulated by factors in the different tissue microenvironments.

Additional Information

© 1995 by Cell Press. Received 15 March 1995, Revised 9 June 1995. This work was supported by grants Al-22346, Al-22531, Al-23483, Al-31599, AR-07530, AR-36308, RR-05950, HL-48598, and HL-36110 from the National Institutes of Health, and by a grant from the Hyde and Watson Foundation. W. S. P. was supported by a physician postdoctoral fellowship from the Howard Hughes Medical Institute. We thank Mr. B. Soffer for technical assistance, Dr. J. Flanagan (Harvard Medical School) for the c-kit cDNA, and Dr. N. Rosenberg (Tufts Medical School) for the 24-21 anti-abl monoclonal antibody.

Additional details

Created:
August 20, 2023
Modified:
October 20, 2023