| Literature DB >> 31434755 |
Christophe Lechauve1, Julia Keith1, Eugene Khandros2, Stephanie Fowler1, Kalin Mayberry1, Abdullah Freiwan1, Christopher S Thom3, Paola Delbini4,5, Emilio Boada Romero6, Jingjing Zhang1, Irene Motta4,5, Heather Tillman7, M Domenica Cappellini4,5, Mondira Kundu8, Mitchell J Weiss9.
Abstract
In β-thalassemia, accumulated free α-globin forms intracellular precipitates that impair erythroid cell maturation and viability. Protein quality control systems mitigate β-thalassemia pathophysiology by degrading toxic free α-globin, although the associated mechanisms are poorly understood. We show that loss of the autophagy-activating Unc-51-like kinase 1 (Ulk1) gene in β-thalassemic mice reduces autophagic clearance of α-globin in red blood cell precursors and exacerbates disease phenotypes, whereas inactivation of the canonical autophagy-related 5 (Atg5) gene has relatively minor effects. Systemic treatment with the mTORC1 inhibitor rapamycin reduces α-globin precipitates and lessens pathologies in β-thalassemic mice via an ULK1-dependent pathway. Similarly, rapamycin reduces free α-globin accumulation in erythroblasts derived from CD34+ cells of β-thalassemic individuals. Our findings define a drug-regulatable pathway for ameliorating β-thalassemia.Entities:
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Year: 2019 PMID: 31434755 PMCID: PMC7441525 DOI: 10.1126/scitranslmed.aav4881
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956