bcl-x prevents apoptotic cell death of both primitive and definitive erythrocytes at the end of maturation

Citation
N. Motoyama et al., bcl-x prevents apoptotic cell death of both primitive and definitive erythrocytes at the end of maturation, J EXP MED, 189(11), 1999, pp. 1691-1698
Citations number
43
Categorie Soggetti
Medical Research General Topics
Journal title
JOURNAL OF EXPERIMENTAL MEDICINE
ISSN journal
00221007 → ACNP
Volume
189
Issue
11
Year of publication
1999
Pages
1691 - 1698
Database
ISI
SICI code
0022-1007(19990607)189:11<1691:BPACDO>2.0.ZU;2-F
Abstract
bcl-x is a member of the bcl-2 gene family, which regulates apoptotic cell death in various cell lineages. There is circumstantial evidence suggesting that bcl-x might play a role in the apoptosis of erythroid lineage cells, although there is no direct evidence. In this study, we used Bcl-X null mou se embryonic stem (ES) cells, and showed that Bcl-X is indispensable for th e production of both embryonic primitive erythrocytes (EryP) and adult defi nitive erythrocytes (EryD) at the end of their maturation. In vivo, bcl-x(- /-) ES cells did not contribute to circulating EryD in adult chimeric mice that were produced by blastocyst microinjection of the bcl-x-/- ES cells, b cl-x-/- EryP and EryD were produced by in vitro differentiation induction o f ES cells on macrophage colony-stimulating factor-deficient stromal cell l ine OP9, and further analysis was carried out. The emergence of immature Er yP and EryD from bcl-x-/- ES cells was similar to that from bcl-x(+/+) ES c ells. However, prominent cell death of bcl-x(-/-) EryP and EryD occurred wh en the cells matured. The data show that the antiapoptotic function of bcl- x acts at the very end of erythroid maturation.