Skip to main content

Growth hormone mitigates against lethal irradiation and enhances hematologic and immune recovery in mice and nonhuman primates.

Publication ,  Journal Article
Chen, BJ; Deoliveira, D; Spasojevic, I; Sempowski, GD; Jiang, C; Owzar, K; Wang, X; Gesty-Palmer, D; Cline, JM; Bourland, JD; Dugan, G ...
Published in: PLoS One
June 16, 2010

Medications that can mitigate against radiation injury are limited. In this study, we investigated the ability of recombinant human growth hormone (rhGH) to mitigate against radiation injury in mice and nonhuman primates. BALB/c mice were irradiated with 7.5 Gy and treated post-irradiation with rhGH intravenously at a once daily dose of 20 microg/dose for 35 days. rhGH protected 17 out of 28 mice (60.7%) from lethal irradiation while only 3 out of 28 mice (10.7%) survived in the saline control group. A shorter course of 5 days of rhGH post-irradiation produced similar results. Compared with the saline control group, treatment with rhGH on irradiated BALB/c mice significantly accelerated overall hematopoietic recovery. Specifically, the recovery of total white cells, CD4 and CD8 T cell subsets, B cells, NK cells and especially platelets post radiation exposure were significantly accelerated in the rhGH-treated mice. Moreover, treatment with rhGH increased the frequency of hematopoietic stem/progenitor cells as measured by flow cytometry and colony forming unit assays in bone marrow harvested at day 14 after irradiation, suggesting the effects of rhGH are at the hematopoietic stem/progenitor level. rhGH mediated the hematopoietic effects primarily through their niches. Similar data with rhGH were also observed following 2 Gy sublethal irradiation of nonhuman primates. Our data demonstrate that rhGH promotes hematopoietic engraftment and immune recovery post the exposure of ionizing radiation and mitigates against the mortality from lethal irradiation even when administered after exposure.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

June 16, 2010

Volume

5

Issue

6

Start / End Page

e11056

Location

United States

Related Subject Headings

  • T-Lymphocyte Subsets
  • Recombinant Proteins
  • Radiation Injuries, Experimental
  • Primates
  • Mice, Inbred C57BL
  • Mice, Inbred BALB C
  • Mice
  • Growth Hormone
  • General Science & Technology
  • Apoptosis
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Chen, B. J., Deoliveira, D., Spasojevic, I., Sempowski, G. D., Jiang, C., Owzar, K., … Chao, N. J. (2010). Growth hormone mitigates against lethal irradiation and enhances hematologic and immune recovery in mice and nonhuman primates. PLoS One, 5(6), e11056. https://doi.org/10.1371/journal.pone.0011056
Chen, Benny J., Divino Deoliveira, Ivan Spasojevic, Gregory D. Sempowski, Chen Jiang, Kouros Owzar, Xiaojuan Wang, et al. “Growth hormone mitigates against lethal irradiation and enhances hematologic and immune recovery in mice and nonhuman primates.PLoS One 5, no. 6 (June 16, 2010): e11056. https://doi.org/10.1371/journal.pone.0011056.
Chen BJ, Deoliveira D, Spasojevic I, Sempowski GD, Jiang C, Owzar K, et al. Growth hormone mitigates against lethal irradiation and enhances hematologic and immune recovery in mice and nonhuman primates. PLoS One. 2010 Jun 16;5(6):e11056.
Chen, Benny J., et al. “Growth hormone mitigates against lethal irradiation and enhances hematologic and immune recovery in mice and nonhuman primates.PLoS One, vol. 5, no. 6, June 2010, p. e11056. Pubmed, doi:10.1371/journal.pone.0011056.
Chen BJ, Deoliveira D, Spasojevic I, Sempowski GD, Jiang C, Owzar K, Wang X, Gesty-Palmer D, Cline JM, Bourland JD, Dugan G, Meadows SK, Daher P, Muramoto G, Chute JP, Chao NJ. Growth hormone mitigates against lethal irradiation and enhances hematologic and immune recovery in mice and nonhuman primates. PLoS One. 2010 Jun 16;5(6):e11056.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

June 16, 2010

Volume

5

Issue

6

Start / End Page

e11056

Location

United States

Related Subject Headings

  • T-Lymphocyte Subsets
  • Recombinant Proteins
  • Radiation Injuries, Experimental
  • Primates
  • Mice, Inbred C57BL
  • Mice, Inbred BALB C
  • Mice
  • Growth Hormone
  • General Science & Technology
  • Apoptosis