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Erythroid dysplasia, megaloblastic anemia, and impaired lymphopoiesis arising from mitochondrial dysfunction

  • Michael L. Chen
  • , T. Daniel Logan
  • , Maryann L. Hochberg
  • , Suresh G. Shelat
  • , Xiang Yu
  • , Gregory E. Wilding
  • , Wei Tan
  • , Gregory C. Kujoth
  • , Tomas A. Prolla
  • , Mary A. Selak
  • , Mondira Kundu
  • , Martin Carroll
  • , James E. Thompson
  • University of Pennsylvania
  • Roswell Park Cancer Institute
  • University of Wisconsin-Madison
  • St. Jude Children Research Hospital

Research output: Contribution to journalArticlepeer-review

97 Scopus citations

Abstract

Recent reports describe hematopoietic abnormalities in mice with targeted instability of the mitochondrial genome. However, these abnormalities have not been fully described. We demonstrate that mutant animals develop an age-dependent, macrocytic anemia with abnormal erythroid maturation and megaloblastic changes, as well as profound defects in lymphopoiesis. Mice die of severe fatal anemia at 15 months of age. Bonemarrow transplantation studies demonstrate that these abnormalities are intrinsic to the hematopoietic compartment and dependent upon the age of donor hematopoietic stem cells. These abnormalities are phenotypically similar to those found in patients with refractory anemia, suggesting that, in some cases, the myelodysplastic syndromes are caused by abnormalities of mitochondrial function.

Original languageEnglish
Pages (from-to)4045-4053
Number of pages9
JournalBlood
Volume114
Issue number19
DOIs
StatePublished - Nov 5 2009

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