抄録
We have previously shown that the common progenitors for myeloid, T, and B cell lineages are enriched in the earliest population of murine fetal liver. However, it remained unclear whether such multipotent progenitors represent the pluripotent progenitors capable of generating all hemopoietic cells or they also comprise progenitors restricted to myeloid, T, and B cell lineages. To address this issue, we have developed a new clonal assay covering myeloid, erythroid, T, and B cell lineages, and using this assay the developmental potential of individual cells in subpopulations of lineage marker-negative (Lin-) c-kit+ murine fetal liver cells was investigated. We identified the progenitor generating myeloid, T, and B cells, but not erythroid cells in the Sca-1high subpopulation of Linc-kit+ cells that can thus be designated as the common myelolymphoid progenitor (CMLP). Common myeloerythroid progenitors were also detected. These findings strongly suggest that the first branching point in fetal hemopoiesis is between the CMLP and common myeloerythroid progenitors. T and B cell progenitors may be derived from the CMLP through the previously identified myeloid/T and myeloid/B bipotent stages, respectively.
| 本文言語 | 英語 |
|---|---|
| ページ(範囲) | 3519-3525 |
| ページ数 | 7 |
| ジャーナル | Journal of Immunology |
| 巻 | 169 |
| 号 | 7 |
| DOI | |
| 出版ステータス | 出版済み - 01-10-2002 |
All Science Journal Classification (ASJC) codes
- 免疫アレルギー学
- 免疫学
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