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Identification of mast cell progenitors in adult mice
Abstract
It is well known that mast cells are derived from hematopoietic stem cells. However, in adult hematopoiesis, a committed mast cell progenitor has not yet been identified in any species, nor is it clear at what point during adult hematopoiesis commitment to the mast cell lineage occurs. We identified a cell population in adult mouse bone marrow, characterized as Lin - c-Kit + Sca-1 - -Ly6c - FcεRIα - CD27 - β7 + T1/ST2 + , that gives rise only to mast cells in culture and that can reconstitute the mast cell compartment when transferred into c- kit mutant mast cell-deficient mice. In addition, our experiments strongly suggest that these adult mast cell progenitors are derived directly from multipotential progenitors instead of, as previously proposed, common myeloid progenitors or granulocyte/macrophage progenitors.
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“Integrin α4β7 specifically is expressed by adult BM progenitors with mast cell potential 64 and required for gut homing of mast cell progenitors. 65”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [64]
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“In both mice 64 , 73 and humans, 74 , 75 BM HSCs produce mast cells in a stepwise process from multipotent (MPP) to lineage‐committed progenitors via common myeloid (CMP) and granulocyte‐monocyte progenitor (GMP) intermediates. 76 , 77”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [64]
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“Decades of work have established that progenitors with mast cell differentiation potential exist in the adult BM.”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [64]
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Cites
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Self-citationTHE HIGH-AFFINITY I g E RECEPTOR (FcεRI): From Physiology to Pathology
Kinet, J.-P. (1999) · Annual Review of Immunology · doi:10.1146/annurev.immunol.17.1.931 · Cited by 968
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Mast cell ontogeny: From fetal development to life‐long health and disease
Chia, S. L., Kapoor, S., Carvalho, C., Bajénoff, M., & Gentek, R. (2023) · Immunological Reviews · doi:10.1111/imr.13191 · Cited by 60
Guo, M. H., Nandakumar, S. K., Ulirsch, J. C., Zekavat, S. M., Buenrostro, J. D., Natarajan, P., Salem, R. M., Chiarle, R., Mitt, M., Kals, M., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619052114 · Cited by 54
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Metadata
- Authors
- Chen, C.-C., Grimbaldeston, M. A., Tsai, M., Weissman, I. L., & Galli, S. J.
- Affiliations
- Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305-5324
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2005-07-08
- Volume
- 102
- Issue
- 32
- Pages
- 11408-11413
- ISSN
- 0027-8424
- 1091-6490
- Cited by
- 269
- References
- 2
- Language
- en
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