| First Author | Liu K | Year | 2022 |
| Journal | J Cell Biol | Volume | 221 |
| Issue | 6 | PubMed ID | 35482005 |
| Mgi Jnum | J:331898 | Mgi Id | MGI:7408018 |
| Doi | 10.1083/jcb.202108093 | Citation | Liu K, et al. (2022) Lineage tracing clarifies the cellular origin of tissue-resident macrophages in the developing heart. J Cell Biol 221(6) |
| abstractText | Tissue-resident macrophages play essential functions in the maintenance of tissue homeostasis and repair. Recently, the endocardium has been reported as a de novo hemogenic site for the contribution of hematopoietic cells, including cardiac macrophages, during embryogenesis. These observations challenge the current consensus that hematopoiesis originates from the hemogenic endothelium within the yolk sac and dorsal aorta. Whether the developing endocardium has such a hemogenic potential requires further investigation. Here, we generated new genetic tools to trace endocardial cells and reassessed their potential contribution to hematopoietic cells in the developing heart. Fate-mapping analyses revealed that the endocardium contributed minimally to cardiac macrophages and circulating blood cells. Instead, cardiac macrophages were mainly derived from the endothelium during primitive/transient definitive (yolk sac) and definitive (dorsal aorta) hematopoiesis. Our findings refute the concept of endocardial hematopoiesis, suggesting that the developing endocardium gives rise minimally to hematopoietic cells, including cardiac macrophages. |
