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Mol Genet Metab. 2016 Sep;119(1-2):28-36. doi: 10.1016/j.ymgme.2016.07.004. Epub 2016 Jul 15.

Aldehyde dehydrogenase 2 in aplastic anemia, Fanconi anemia and hematopoietic stem cells.

Author information

1
Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA. Electronic address: ldvanwas@stanford.edu.
2
Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA.
3
Division of Stem Cell Biology and Regenerative Medicine, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.

Abstract

Maintenance of the hematopoietic stem cell (HSC) compartment depends on the ability to metabolize exogenously and endogenously generated toxins, and to repair cellular damage caused by such toxins. Reactive aldehydes have been demonstrated to cause specific genotoxic injury, namely DNA interstrand cross-links. Aldehyde dehydrogenase 2 (ALDH2) is a member of a 19 isoenzyme ALDH family with different substrate specificities, subcellular localization, and patterns of expression. ALDH2 is localized in mitochondria and is essential for the metabolism of acetaldehyde, thereby placing it directly downstream of ethanol metabolism. Deficiency in ALDH2 expression and function are caused by a single nucleotide substitution and resulting amino acid change, called ALDH2*2. This genetic polymorphism affects 35-45% of East Asians (about ~560 million people), and causes the well-known Asian flushing syndrome, which results in disulfiram-like reactions after ethanol consumption. Recently, the ALDH2*2 genotype has been found to be associated with marrow failure, with both an increased risk of sporadic aplastic anemia and more rapid progression of Fanconi anemia. This review discusses the unexpected interrelationship between aldehydes, ALDH2 and hematopoietic stem cell biology, and in particular its relationship to Fanconi anemia.

KEYWORDS:

ALDH2; Aldehyde dehydrogenase; Aldehydes; Aplastic anemia; Fanconi anemia; Hematopoiesis; Hematopoietic stem cell

PMID:
27650066
PMCID:
PMC5082284
DOI:
10.1016/j.ymgme.2016.07.004
[Indexed for MEDLINE]
Free PMC Article

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