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Carboxy-terminal fragment of osteogenic growth peptide regulates myeloid differentiation through RhoA
- Source :
- Journal of Cellular Biochemistry. 93:1231-1241
- Publication Year :
- 2004
- Publisher :
- Wiley, 2004.
-
Abstract
- The carboxy-terminal fragment of osteogenic growth peptide, OGP(10-14), is a pentapeptide with bone anabolic effects and hematopoietic activity. The latter activity appears to be largely enhanced by specific growth factors. To study the direct activity of OGP(10-14) on myeloid cells, we tested the pentapeptide proliferating/differentiating effects in HL60 cell line. In this cell line, OGP(10-14) significantly inhibited cell proliferation, and enhanced myeloperoxidase (MPO) activity and nitroblue tetrazolium reducing ability. Moreover, it induced cytoskeleton remodeling and small GTP-binding protein RhoA activation. RhoA, which is known to be involved in HL60 differentiation, mediated these effects as shown by using its specific inhibitor, C3. Treatment with GM-CSF had a comparable OGP(10-14) activity on proliferation, MPO expression, and RhoA activation. Further studies on cell proliferation and RhoA activation proved enhanced activity by association of the two factors. These results strongly suggest that OGP(10-14) acts directly on HL60 cells by activating RhoA signaling although other possibilities cannot be ruled out.
- Subjects :
- RHOA
HL60
OGP(10–14)
Cellular differentiation
OGP(10–14),GM-CSF,RhoA,HL60,cell differentiation
HL-60 Cells
Biochemistry
Pentapeptide repeat
Histones
chemistry.chemical_compound
Humans
Myeloid Cells
Molecular Biology
Cell Proliferation
Peroxidase
biology
Cell growth
Nitroblue Tetrazolium
GM-CSF
RhoA
Cell Biology
Molecular biology
Actins
cell differentiation
Haematopoiesis
chemistry
Cell culture
Myeloperoxidase
biology.protein
Intercellular Signaling Peptides and Proteins
rhoA GTP-Binding Protein
Subjects
Details
- ISSN :
- 10974644 and 07302312
- Volume :
- 93
- Database :
- OpenAIRE
- Journal :
- Journal of Cellular Biochemistry
- Accession number :
- edsair.doi.dedup.....bee4856b42e1824935d26de0d74aee5b
- Full Text :
- https://doi.org/10.1002/jcb.20248