Mitigating effects of hUCB-MSCs on the hematopoietic syndrome resulting from total body irradiation

Exp Hematol. 2013 Apr;41(4):346-53.e2. doi: 10.1016/j.exphem.2013.01.002. Epub 2013 Jan 17.

Abstract

This study evaluated the clinical and pathologic effects of human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs) in the recovery from total body irradiation by comparing it with the effects of granulocyte-colony stimulating factor (G-CSF), an efficacious drug in the treatment of acute bone marrow radiation syndrome. BALB/c mice were treated with G-CSF or hUCB-MSCs after they were irradiated with 7 Gy cobalt-60 γ-rays. Circulating blood counts, histopathologic changes in the bone marrow, and plasma level of Flt-3L and transforming growth factor (TGF-β1) were monitored in the postirradiation period. Hematologic analysis revealed that the peripheral leukocyte counts were markedly increased in the hUCB-MSCs-treated group, whereas G-CSF-treated mice did not recover significantly. Moreover, differential counts showed that hUCB-MSC treatment has regenerative effects on white blood cells, lymphocytes, and monocytes compared with the irradiated group. Treatment with hUCB-MSCs or G-CSF significantly increased immunoreactivity of Ki-67 until 3 weeks after total body irradiation. However, at 3 weeks, the number of Ki-67 immunoreactive cells significantly increased in the hUCB-MSCs-treated group compared with the G-CSF-treated group. Furthermore, hUCB-MSC treatment significantly modulated plasma levels of the hematopoietic cytokines Flt-3L and TGF-β1, whereas G-CSF treatment failed to decrease the plasma Flt-3L levels at 2 weeks after irradiation. Based on the differences in circulating blood cell reconstitution and cell density of bone marrow, the authors suggest that MSC treatment is superior to G-CSF treatment for hematopoietic reconstitution following sublethal dose radiation exposure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Radiation Syndrome / drug therapy
  • Acute Radiation Syndrome / etiology
  • Acute Radiation Syndrome / surgery*
  • Animals
  • Bone Marrow / drug effects
  • Bone Marrow / pathology*
  • Bone Marrow / radiation effects
  • Cells, Cultured
  • Female
  • Fetal Blood / cytology
  • Gamma Rays / adverse effects
  • Granulocyte Colony-Stimulating Factor / pharmacology
  • Humans
  • Ki-67 Antigen / metabolism
  • Leukocyte Count
  • Mesenchymal Stem Cell Transplantation / methods*
  • Mesenchymal Stem Cells / cytology
  • Mice
  • Mice, Inbred BALB C
  • Radiation Injuries, Experimental / drug therapy
  • Radiation Injuries, Experimental / etiology
  • Radiation Injuries, Experimental / surgery*
  • Time Factors
  • Transforming Growth Factor beta1 / blood
  • Transplantation, Heterologous
  • Treatment Outcome
  • Whole-Body Irradiation / adverse effects
  • fms-Like Tyrosine Kinase 3 / blood

Substances

  • Ki-67 Antigen
  • Transforming Growth Factor beta1
  • Granulocyte Colony-Stimulating Factor
  • Flt3 protein, mouse
  • fms-Like Tyrosine Kinase 3