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Synthesis of membrane‐ and matrix‐bound colony‐stimulating factor‐1 by cultured osteoblasts

Synthesis of membrane‐ and matrix‐bound colony‐stimulating factor‐1 by cultured osteoblasts 10.1002/(SICI)1097-4652(199602)166:2<311::AID-JCP9>3.3.CO;2-U Colony‐stimulating factor‐1 (CSF‐1) is synthesized as a secreted or membrane‐bound molecule. We investigated whether osteoblastic cells produce these forms of CSF‐1. Glutaraldehyde‐fixed cell layers supported proliferation of the macrophage cell line BAC1.2F5, suggesting the presence of membrane‐ or/and matrix‐associated CSF‐1. Furthermore, CSF‐1 activity could be either extracted from the matrix or released from the cell membrane. A neutralizing antiserum against CSF‐1 inhibited these activities. After labeling the cellular proteins with (35S) met/cys or (35S) SO2−4, CSF‐1 was immunoprecipitated and analyzed by SDS‐PAGE. Under nonreducing conditions, bands with MW more than 200, 200, 100, and 50 kd were detected. These bands shifted to lower MW under reducing conditions. Treatment with chondroitin lyase ABC decreased the MW of the 200 kd monomer, proving the proteoglycan structure. Much smaller quantities of CSF‐1 were found in the matrix extract than in the conditioned medium. Transforming growth factor β (TGF‐β) increased both the synthesis of CSF‐1 and its accumulation in the matrix. CSF‐1 released with trypsin from the membrane fraction yielded on SDS‐PAGE a band with MW of 60 and 30 kd under nonreducing and reducing conditions, respectively. Transcripts encoding both the secreted and the membrane‐associated forms of the cytokine were detected in osteoblasts by reverse transcription polymerase chain reaction. These data indicate that osteoblastic cells produce the secreted forms, either remaining in the culture supernatant, or being associated to the matrix, and the membrane associated form of CSF‐1. © 1996 Wiley‐Liss, Inc. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Cellular Physiology Wiley

Synthesis of membrane‐ and matrix‐bound colony‐stimulating factor‐1 by cultured osteoblasts

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References (48)

Publisher
Wiley
Copyright
Copyright © 1996 Wiley‐Liss, Inc.
ISSN
0021-9541
eISSN
1097-4652
DOI
10.1002/(SICI)1097-4652(199602)166:2<311::AID-JCP9>3.0.CO;2-S
pmid
8591991
Publisher site
See Article on Publisher Site

Abstract

10.1002/(SICI)1097-4652(199602)166:2<311::AID-JCP9>3.3.CO;2-U Colony‐stimulating factor‐1 (CSF‐1) is synthesized as a secreted or membrane‐bound molecule. We investigated whether osteoblastic cells produce these forms of CSF‐1. Glutaraldehyde‐fixed cell layers supported proliferation of the macrophage cell line BAC1.2F5, suggesting the presence of membrane‐ or/and matrix‐associated CSF‐1. Furthermore, CSF‐1 activity could be either extracted from the matrix or released from the cell membrane. A neutralizing antiserum against CSF‐1 inhibited these activities. After labeling the cellular proteins with (35S) met/cys or (35S) SO2−4, CSF‐1 was immunoprecipitated and analyzed by SDS‐PAGE. Under nonreducing conditions, bands with MW more than 200, 200, 100, and 50 kd were detected. These bands shifted to lower MW under reducing conditions. Treatment with chondroitin lyase ABC decreased the MW of the 200 kd monomer, proving the proteoglycan structure. Much smaller quantities of CSF‐1 were found in the matrix extract than in the conditioned medium. Transforming growth factor β (TGF‐β) increased both the synthesis of CSF‐1 and its accumulation in the matrix. CSF‐1 released with trypsin from the membrane fraction yielded on SDS‐PAGE a band with MW of 60 and 30 kd under nonreducing and reducing conditions, respectively. Transcripts encoding both the secreted and the membrane‐associated forms of the cytokine were detected in osteoblasts by reverse transcription polymerase chain reaction. These data indicate that osteoblastic cells produce the secreted forms, either remaining in the culture supernatant, or being associated to the matrix, and the membrane associated form of CSF‐1. © 1996 Wiley‐Liss, Inc.

Journal

Journal of Cellular PhysiologyWiley

Published: Feb 1, 1996

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