The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Characterization of mouse clonogenic megakaryocyte progenitors
Open accessAbstract
Although it has been shown that unfractionated bone marrow, hematopoietic stem cells, common myeloid progenitors, and bipotent megakaryocyte/erythrocyte progenitors can give rise to megakaryocyte colonies in culture, monopotent megakaryocyte-committed progenitors (MKP) have never been prospectively isolated from the bone marrow of adult mice. Here, we use a monoclonal antibody to the megakaryocyte-associated surface protein, CD9, to purify MKPs from the c-kit + Sca-1 − IL7Rα − Thy1.1 − Lin − fraction of adult C57BL/Ka-Thy1.1 bone marrow. The CD9 + fraction contained a subset of CD41 + FcγR lo CD34 + CD38 + cells that represent ≈0.01% of the total nucleated bone marrow cells. They give rise mainly to colony-forming unit–megakaryocytes and occasionally burst-forming unit–megakaryocytes, with a plating efficiency >60% at the single-cell level. In vivo , MKPs do not have spleen colony-forming activity nor do they contribute to long-term multilineage hematopoiesis; they give rise only to platelets for ≈3 weeks. Common myeloid progenitors and megakaryocyte/erythrocyte progenitors can differentiate into MKPs after 72 h in stromal cultures, indicating that MKPs are downstream of these two progenitors. These isolatable MKPs will be very useful for further studies of megakaryopoiesis as well as the elucidation of their gene expression patterns.
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Cites
A clonogenic common myeloid progenitor that gives rise to all myeloid lineages
Akashi, K., Traver, D., Miyamoto, T., & Weissman, I. L. (2000) · Nature · doi:10.1038/35004599 · Cited by 2,617
Self-citationStem and progenitor cells: origins, phenotypes, lineage commitments, and transdifferentiations
Weissman, I. L., Anderson, D. J., & Gage, F. (2001) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.17.1.387 · Cited by 948
Self-citationWright, D. E., Cheshier, S. H., Wagers, A. J., Randall, T. D., Christensen, J. L., & Weissman, I. L. (2001) · Blood · doi:10.1182/blood.v97.8.2278 · Cited by 208
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Cited by
Kiel, M. J., Yilmaz, Ö. H., Iwashita, T., Yilmaz, O. H., Terhorst, C., & Morrison, S. J. (2005) · Cell · doi:10.1016/j.cell.2005.05.026 · Cited by 3,168
BCG Educates Hematopoietic Stem Cells to Generate Protective Innate Immunity against Tuberculosis
Kaufmann, E., Sanz, J., Dunn, J. L., Khan, N., Mendonça, L. E., Pacis, A., Tzelepis, F., Pernet, E., Dumaine, A., Grenier, J.-C., et al. (2018) · Cell · doi:10.1016/j.cell.2017.12.031 · Cited by 1,191
Hematopoietic stem cell: self‐renewal versus differentiation
Seita, J., & Weissman, I. L. (2010) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.86 · Cited by 932
Self-citationPronk, C. J. H., Rossi, D. J., Månsson, R., Attema, J. L., Norddahl, G. L., Chan, C. K. F., Sigvardsson, M., Weissman, I. L., & Bryder, D. (2007) · Cell Stem Cell · doi:10.1016/j.stem.2007.07.005 · Cited by 671
Self-citationMyeloid Lineage Commitment from the Hematopoietic Stem Cell
Iwasaki, H., & Akashi, K. (2007) · Immunity · doi:10.1016/j.immuni.2007.06.004 · Cited by 394
Metadata
- Authors
- Nakorn, T. N., Miyamoto, T., & Weissman, I. L.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2002-12-18
- Volume
- 100
- Issue
- 1
- Pages
- 205-210
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2010934897
- Cited by
- 166
- References
- 3
- FWCI
- 3.47
- Type
- journal article
- Language
- en
- Open access
- green
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