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Identification of a Committed Precursor for the Mast Cell Lineage
Abstract
Mast cells originate from hematopoietic stem cells, but the mast cell-committed precursor has not been identified. In the study presented here, a cell population in murine fetal blood that fulfills the criteria of progenitor mastocytes was identified. It is defined by the phenotype Thy-1 lo c-Kit hi , contains cytoplasmic granules, and expresses RNAs encoding mast cell-associated proteases but lacks expression of the high-affinity immunoglobulin E receptor. Thy-1 lo c-Kit hi cells generated functionally competent mast cells at high frequencies in vitro but lacked developmental potential for other hematopoietic lineages. When transferred intraperitoneally, this population reconstituted the peritoneal mast cell compartment of genetically mast cell-deficient W / W v mice to wild-type levels.
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In the citing paper
“In vitro, they efficiently produce mast cell colonies, but not any other lineages.”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [52]
In the citing paper
“In vivo, they repopulate peritoneal mast cells upon intra‐peritoneal injection into deficient W/Wv recipients.”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [52]
In the citing paper
“Finally, work from the 1990 s described a population of lineage‐committed cells present in the fetal blood. 52”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [52]
In the citing paper
“These Kithigh Thy1low cells are first detected at E14.5, peak in numbers at E15.5 and decline towards birth.”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [52]
In the citing paper
“These were phenotypically identified by high expression of Kit, low‐level expression of Thy1 and a low density of granules. They also express transcripts for three different mast cell proteases, Cpa3, Mcpt2, and Mcpt4.”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [52]
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Metadata
- Authors
- Rodewald, H.-R., Dessing, M., Dvorak, A. M., & Galli, S. J.
- Affiliations
- H.-R. Rodewald and M. Dessing, Basel Institute for Immunology, Grenzacherstrasse 487, CH-4005 Basel, Switzerland.
- A. M. Dvorak and S. J. Galli, Department of Pathology, Beth Israel Hospital, Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA.
- Venue
- Science
- Published
- 1996-02-09
- Volume
- 271
- Issue
- 5250
- Pages
- 818-822
- ISSN
- 0036-8075
- 1095-9203
- Cited by
- 285
- References
- 0
- Language
- en
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