Evaluation of erythroblast macrophage protein related to erythroblastic islands in patients with hematopoietic stem cell transplantation

Eur J Med Res. 2013 Apr 8;18(1):9. doi: 10.1186/2047-783X-18-9.

Abstract

Background: Hematopoietic evaluation of the patients after Hematopoietic stem cell transplantation (HSCT) is very important. Erythroblast macrophage protein (Emp) is a key protein with function in normal differentiation of erythroid cells and macrophages. Emp expression correlates with erythroblastic island formation, a process widely believed to be associated with hematopoiesis in bone marrow. We aimed to investigate the hematopoietic function of bone marrow from 46 HSCT patients and 16 inpatients with severe anemia applied to the treatment of EPO by measuring Emp expression level.

Methods: Emp mRNA and protein expression levels in mononuclear cells of bone marrow and peripheral blood samples were detected by RT-PCR and Western blotting method respectively.

Results: While hematopoiesis occurs in bone marrow, Emp expression level was elevated and more erythroblastic islands were found , and Emp is upregulated in bone marrow in response to erythropoietin (EPO) treatment.

Conclusions: Emp expression correlates with erythroblastic island formation and has an important function for bone marrow hematopoiesis. Emp could be a potential biomarker for hematopoietic evaluation of HSCT patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Bone Marrow / drug effects
  • Bone Marrow / metabolism
  • Bone Marrow / pathology
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism*
  • Cell Shape / drug effects
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism*
  • Erythroblasts / drug effects
  • Erythroblasts / metabolism*
  • Erythropoietin / administration & dosage
  • Erythropoietin / pharmacology
  • Female
  • Gene Expression Regulation / drug effects
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Hyperplasia
  • Immunosuppression Therapy
  • Male
  • Young Adult

Substances

  • Cell Adhesion Molecules
  • Cytoskeletal Proteins
  • MAEA protein, human
  • Erythropoietin