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Radiation effects and radioprotection in MC3T3-E1 mouse calvarial osteoblastic cells.

Publication ,  Journal Article
Gevorgyan, A; Sukhu, B; Alman, BA; Bristow, RG; Pang, CY; Forrest, CR
Published in: Plast Reconstr Surg
October 2008

BACKGROUND: Little is known about the mechanisms and treatment of radiation-induced inhibition of craniofacial bone growth. In an earlier study, the radioprotector amifostine (WR-2721) administered to rabbits before irradiation radioprotected cultured orbitozygomatic complex periosteal osteoblast-like cells. This study assessed the effects of amifostine and its active metabolite on the radiation survival, function, and phenotype of mouse calvarial osteoblast-like cells in a cell culture model. METHODS: MC3T3-E1 newborn mouse calvarial osteoblast-like cells underwent gamma-radiation (0 to 10 Gy) in the presence or absence of either WR-2721 or WR-1065, its active metabolite (10 to 10 M). The effects of radiation with and without drugs were assessed using endpoints of colony-forming ability, cell viability, alkaline phosphatase activity, and expression of osteoblastic phenotype genes (alkaline phosphatase, collagen type I, osteocalcin, and osteopontin). All experiments were replicated at least in triplicate. RESULTS: Irradiation resulted in a dose-dependent inhibition of clonogenic cell survival. Pretreatment with WR-1065, but not WR-2721, resulted in a significant improvement of osteoblast-like cell survival. Specifically, maximum radioprotection was observed with 10 M WR-1065 at a clinically relevant 2-Gy dose of irradiation. No significant radioprotection was observed at the lower (5 x 10 M) concentration of WR-1065. Furthermore, radiation seemed to suppress the expression of osteoblastic phenotype-related genes in a dose-dependent manner. CONCLUSIONS: This study reveals improved survival after irradiation in osteoblast-like cells treated with WR-1065 in vitro and corroborates previous findings from animal models. Further studies using this agent and similar drugs are important for devising strategies to prevent radiation-induced inhibition of craniofacial bone growth.

Duke Scholars

Published In

Plast Reconstr Surg

DOI

EISSN

1529-4242

Publication Date

October 2008

Volume

122

Issue

4

Start / End Page

1025 / 1035

Location

United States

Related Subject Headings

  • Surgery
  • Skull
  • Radiation-Protective Agents
  • Osteoblasts
  • Models, Animal
  • Mice
  • Gamma Rays
  • Cell Line
  • Animals, Newborn
  • Animals
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Gevorgyan, A., Sukhu, B., Alman, B. A., Bristow, R. G., Pang, C. Y., & Forrest, C. R. (2008). Radiation effects and radioprotection in MC3T3-E1 mouse calvarial osteoblastic cells. Plast Reconstr Surg, 122(4), 1025–1035. https://doi.org/10.1097/PRS.0b013e3181845931
Gevorgyan, Artur, Balram Sukhu, Benjamin A. Alman, Robert G. Bristow, Cho Y. Pang, and Christopher R. Forrest. “Radiation effects and radioprotection in MC3T3-E1 mouse calvarial osteoblastic cells.Plast Reconstr Surg 122, no. 4 (October 2008): 1025–35. https://doi.org/10.1097/PRS.0b013e3181845931.
Gevorgyan A, Sukhu B, Alman BA, Bristow RG, Pang CY, Forrest CR. Radiation effects and radioprotection in MC3T3-E1 mouse calvarial osteoblastic cells. Plast Reconstr Surg. 2008 Oct;122(4):1025–35.
Gevorgyan, Artur, et al. “Radiation effects and radioprotection in MC3T3-E1 mouse calvarial osteoblastic cells.Plast Reconstr Surg, vol. 122, no. 4, Oct. 2008, pp. 1025–35. Pubmed, doi:10.1097/PRS.0b013e3181845931.
Gevorgyan A, Sukhu B, Alman BA, Bristow RG, Pang CY, Forrest CR. Radiation effects and radioprotection in MC3T3-E1 mouse calvarial osteoblastic cells. Plast Reconstr Surg. 2008 Oct;122(4):1025–1035.

Published In

Plast Reconstr Surg

DOI

EISSN

1529-4242

Publication Date

October 2008

Volume

122

Issue

4

Start / End Page

1025 / 1035

Location

United States

Related Subject Headings

  • Surgery
  • Skull
  • Radiation-Protective Agents
  • Osteoblasts
  • Models, Animal
  • Mice
  • Gamma Rays
  • Cell Line
  • Animals, Newborn
  • Animals