NIX is required for programmed mitochondrial clearance during reticulocyte maturation
St. Jude Children's Research Hospital · University of Tennessee Health Science Center · +4 more institutions
Abstract
The regulated clearance of mitochondria is a well recognized but poorly understood aspect of cellular homeostasis, and defects in this process have been linked to aging, degenerative diseases, and cancer. Mitochondria are recycled through an autophagy-related process, and reticulocytes, which completely eliminate their mitochondria during maturation, provide a physiological model to study this phenomenon. Here, we show that mitochondrial clearance in reticulocytes requires the BCL2-related protein NIX (BNIP3L). Mitochondrial clearance does not require BAX, BAK, BCL-X(L), BIM, or PUMA, indicating that NIX does not function through established proapoptotic pathways. Similarly, NIX is not required for the…
Citation impact
- FWCI
- 18.46
- Percentile
- 100%
- References
- 44
Authors
11- RLRachel L. SchweersCorresponding
St. Jude Children's Research Hospital
- JZJi Zhang
St. Jude Children's Research Hospital, University of Tennessee Health Science Center
- MSMindy S. Randall
St. Jude Children's Research Hospital
- MRMelanie R. Loyd
St. Jude Children's Research Hospital
- WLWeimin Li
Scripps Research Institute, St. Jude Children's Research Hospital
Topics & keywords
- Autophagy
- Mitochondrion
- Cell biology
- Reticulocyte
- Mitochondrial fission
- Biology
- Programmed cell death
- Puma
- Good health and well-being