The impact of erythroblast enucleation efficiency on the severity of anemia in patients with myelodysplastic syndrome

Cell Commun Signal. 2023 Nov 20;21(1):332. doi: 10.1186/s12964-023-01353-4.

Abstract

Anemia is the most common manifestation in myelodysplastic syndrome (MDS) patients, but the cause of ineffective hematopoiesis is not fully understood. Enucleation is an important event in the maturation process of erythroblasts. According to a series of morphological phenotypes of the pathological development of MDS erythroblasts, we speculate that there may be enucleation disorders. To verify this hypothesis, we cultured MDS bone marrow CD34+ cells in vitro and induced erythroblast development. The results showed that erythroblast enucleation in MDS was significantly lower than that in the normal group, and the rate of enucleation was positively correlated with hemoglobin concentration. Risk stratification of MDS was performed to further analyze the differences in enucleation among the normal group, low-middle risk group and high-risk group. The results showed that the enucleation rate of the high risk group was higher than that of the low-middle risk group but still lower than that of the normal group. Moreover, the expression of pERK and pAKT in MDS erythroblasts in the high risk group was higher than that in the normal group, while the expression of pERK and pAKT in the low-middle risk group was lower than that in the normal group. Furthermore, the enucleation of MDS was positively correlated with the phosphorylation degree of ERK and AKT. In conclusion, this study reveals that the enucleation of erythroblasts is one of the possible causes of anemia in MDS. Video Abstract.

Keywords: Anemia; Enucleation; MAPK/ERK; Myelodysplastic syndrome (MDS); PI3K/AKT.

Publication types

  • Video-Audio Media
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia* / complications
  • Anemia* / metabolism
  • Anemia* / pathology
  • Bone Marrow Cells / pathology
  • Erythroblasts / metabolism
  • Erythroblasts / pathology
  • Humans
  • Myelodysplastic Syndromes* / complications
  • Myelodysplastic Syndromes* / metabolism
  • Risk Factors