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Systemic Administration of Granulocyte Colony-Stimulating Factor for Osteochondral Defect Repair in a Rat Experimental Model

OBJECTIVE: The objective of this study was to assess the effect of granulocyte colony-stimulating factor (G-CSF) on osteochondral defect repair in the rat knee. DESIGN: Twenty-six 12-week-old male Lewis rats were randomly divided into 2 groups. From day 0 to day 4, the G-CSF group received glycosyla...

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Autores principales: Okano, Tadashi, Mera, Hisashi, Itokazu, Maki, Okabe, Takahiro, Koike, Tatsuya, Nakamura, Hiroaki, Wakitani, Shigeyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297080/
https://www.ncbi.nlm.nih.gov/pubmed/26069690
http://dx.doi.org/10.1177/1947603514520628
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author Okano, Tadashi
Mera, Hisashi
Itokazu, Maki
Okabe, Takahiro
Koike, Tatsuya
Nakamura, Hiroaki
Wakitani, Shigeyuki
author_facet Okano, Tadashi
Mera, Hisashi
Itokazu, Maki
Okabe, Takahiro
Koike, Tatsuya
Nakamura, Hiroaki
Wakitani, Shigeyuki
author_sort Okano, Tadashi
collection PubMed
description OBJECTIVE: The objective of this study was to assess the effect of granulocyte colony-stimulating factor (G-CSF) on osteochondral defect repair in the rat knee. DESIGN: Twenty-six 12-week-old male Lewis rats were randomly divided into 2 groups. From day 0 to day 4, the G-CSF group received glycosylated G-CSF, and the control group received phosphate-buffered saline. A 1.5-mm diameter and 1.0-mm deep osteochondral defect was introduced in the patellar groove of the bilateral femur in all rats on day 4. The peripheral blood nucleated cells were counted for 14 days from the first day of injection, the appearance of the cartilage repair was observed histologically and macroscopically for 2, 4, 8, 12, and 24 weeks after surgery. RESULTS: The number of peripheral blood leukocytes increased 3 days and returned to normal levels 7 days after the first injection. Compared with the control group, the G-CSF group had more fibrous and/or bony tissue at earlier points in time. The tissue repair rate, which is defined as the percentage of repaired osteochondral defects, was significantly higher in the G-CSF group 4 weeks after surgery. However, there were no significant differences in the cartilage repair rate and the modified Wakitani score between the 2 groups at each time point. CONCLUSIONS: The defect filling was significantly better in the G-CSF group in the early phases. Our findings suggest that G-CSF may promote the repair of osteochondral defects by mediating an increase in the number of peripheral blood nucleated cells.
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spelling pubmed-42970802015-06-11 Systemic Administration of Granulocyte Colony-Stimulating Factor for Osteochondral Defect Repair in a Rat Experimental Model Okano, Tadashi Mera, Hisashi Itokazu, Maki Okabe, Takahiro Koike, Tatsuya Nakamura, Hiroaki Wakitani, Shigeyuki Cartilage Article OBJECTIVE: The objective of this study was to assess the effect of granulocyte colony-stimulating factor (G-CSF) on osteochondral defect repair in the rat knee. DESIGN: Twenty-six 12-week-old male Lewis rats were randomly divided into 2 groups. From day 0 to day 4, the G-CSF group received glycosylated G-CSF, and the control group received phosphate-buffered saline. A 1.5-mm diameter and 1.0-mm deep osteochondral defect was introduced in the patellar groove of the bilateral femur in all rats on day 4. The peripheral blood nucleated cells were counted for 14 days from the first day of injection, the appearance of the cartilage repair was observed histologically and macroscopically for 2, 4, 8, 12, and 24 weeks after surgery. RESULTS: The number of peripheral blood leukocytes increased 3 days and returned to normal levels 7 days after the first injection. Compared with the control group, the G-CSF group had more fibrous and/or bony tissue at earlier points in time. The tissue repair rate, which is defined as the percentage of repaired osteochondral defects, was significantly higher in the G-CSF group 4 weeks after surgery. However, there were no significant differences in the cartilage repair rate and the modified Wakitani score between the 2 groups at each time point. CONCLUSIONS: The defect filling was significantly better in the G-CSF group in the early phases. Our findings suggest that G-CSF may promote the repair of osteochondral defects by mediating an increase in the number of peripheral blood nucleated cells. SAGE Publications 2014-04 /pmc/articles/PMC4297080/ /pubmed/26069690 http://dx.doi.org/10.1177/1947603514520628 Text en © The Author(s) 2014
spellingShingle Article
Okano, Tadashi
Mera, Hisashi
Itokazu, Maki
Okabe, Takahiro
Koike, Tatsuya
Nakamura, Hiroaki
Wakitani, Shigeyuki
Systemic Administration of Granulocyte Colony-Stimulating Factor for Osteochondral Defect Repair in a Rat Experimental Model
title Systemic Administration of Granulocyte Colony-Stimulating Factor for Osteochondral Defect Repair in a Rat Experimental Model
title_full Systemic Administration of Granulocyte Colony-Stimulating Factor for Osteochondral Defect Repair in a Rat Experimental Model
title_fullStr Systemic Administration of Granulocyte Colony-Stimulating Factor for Osteochondral Defect Repair in a Rat Experimental Model
title_full_unstemmed Systemic Administration of Granulocyte Colony-Stimulating Factor for Osteochondral Defect Repair in a Rat Experimental Model
title_short Systemic Administration of Granulocyte Colony-Stimulating Factor for Osteochondral Defect Repair in a Rat Experimental Model
title_sort systemic administration of granulocyte colony-stimulating factor for osteochondral defect repair in a rat experimental model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297080/
https://www.ncbi.nlm.nih.gov/pubmed/26069690
http://dx.doi.org/10.1177/1947603514520628
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