TY - JOUR
T1 - The novel monoclonal antibody 9F5 reveals expression of a fragment of GPNMB/osteoactivin processed by furin-like protease(s) in a subpopulation of microglia in neonatal rat brain
AU - Kawahara, Kohichi
AU - Hirata, Hiroshi
AU - Ohbuchi, Kengo
AU - Nishi, Kentaro
AU - Maeda, Akira
AU - Kuniyasu, Akihiko
AU - Yamada, Daisuke
AU - Maeda, Takehiko
AU - Tsuji, Akihiko
AU - Sawada, Makoto
AU - Nakayama, Hitoshi
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Numbers 16047224, 18053019, 19390031 (to H.N.), 17790067, 21790114, 23790133 (to K.K.), and grants from Takeda Science Foundation (to K.K.) and Daiichi Sankyo TaNeDS (to K.K.). The authors thank Drs. Kenji Tanaka and Hideo Hagiwara for their valuable advice on immunohistochemistry. They are grateful to Dr. Shinichi Kohsaka for providing the MG5 microglial cell line. They also thank Drs. Seiji Tajiri (Kumamoto University, Japan) and Kinichi Nakashima (Nara Institute of Science and Technology, Japan) for the primary neuronal cell cultures and for the neuroepithelial cell cultures, respectively. Dr. Eisuke Shimizu, Naoki Mishima, Kiyohiro Koga, Tomoko Sumi, and Sumika Yokoo are acknowledged for their technical assistances.
Publisher Copyright:
© 2016 The Authors. Glia Published by Wiley Periodicals, Inc.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - To differentiate subtypes of microglia (MG), we developed a novel monoclonal antibody, 9F5, against one subtype (type 1) of rat primary MG. The 9F5 showed high selectivity for this cell type in Western blot and immunocytochemical analyses and no cross-reaction with rat peritoneal macrophages (Mφ). We identified the antigen molecule for 9F5: the 50- to 70-kDa fragments of rat glycoprotein nonmetastatic melanoma protein B (GPNMB)/osteoactivin, which started at Lys170. In addition, 9F5 immunoreactivity with GPNMB depended on the activity of furin-like protease(s). More important, rat type 1 MG expressed the GPNMB fragments, but type 2 MG and Mφ did not, although all these cells expressed mRNA and the full-length protein for GPNMB. These results suggest that 9F5 reactivity with MG depends greatly on cleavage of GPNMB and that type 1 MG, in contrast to type 2 MG and Mφ, may have furin-like protease(s) for GPNMB cleavage. In neonatal rat brain, amoeboid 9F5+ MG were observed in specific brain areas including forebrain subventricular zone, corpus callosum, and retina. Double-immunοstaining with 9F5 antibody and anti-Iba1 antibody, which reacts with MG throughout the CNS, revealed that 9F5+ MG were a portion of Iba1+ MG, suggesting that MG subtype(s) exist in vivo. We propose that 9F5 is a useful tool to discriminate between rat type 1 MG and other subtypes of MG/Mφ and to reveal the role of the GPNMB fragments during developing brain. GLIA 2016;64:1938–1961.
AB - To differentiate subtypes of microglia (MG), we developed a novel monoclonal antibody, 9F5, against one subtype (type 1) of rat primary MG. The 9F5 showed high selectivity for this cell type in Western blot and immunocytochemical analyses and no cross-reaction with rat peritoneal macrophages (Mφ). We identified the antigen molecule for 9F5: the 50- to 70-kDa fragments of rat glycoprotein nonmetastatic melanoma protein B (GPNMB)/osteoactivin, which started at Lys170. In addition, 9F5 immunoreactivity with GPNMB depended on the activity of furin-like protease(s). More important, rat type 1 MG expressed the GPNMB fragments, but type 2 MG and Mφ did not, although all these cells expressed mRNA and the full-length protein for GPNMB. These results suggest that 9F5 reactivity with MG depends greatly on cleavage of GPNMB and that type 1 MG, in contrast to type 2 MG and Mφ, may have furin-like protease(s) for GPNMB cleavage. In neonatal rat brain, amoeboid 9F5+ MG were observed in specific brain areas including forebrain subventricular zone, corpus callosum, and retina. Double-immunοstaining with 9F5 antibody and anti-Iba1 antibody, which reacts with MG throughout the CNS, revealed that 9F5+ MG were a portion of Iba1+ MG, suggesting that MG subtype(s) exist in vivo. We propose that 9F5 is a useful tool to discriminate between rat type 1 MG and other subtypes of MG/Mφ and to reveal the role of the GPNMB fragments during developing brain. GLIA 2016;64:1938–1961.
KW - GPNMB/osteoactivin
KW - development
KW - microglial heterogeneity
KW - retinal pigment epithelium
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U2 - 10.1002/glia.23034
DO - 10.1002/glia.23034
M3 - Article
C2 - 27464357
AN - SCOPUS:84990849595
SN - 0894-1491
VL - 64
SP - 1938
EP - 1961
JO - GLIA
JF - GLIA
IS - 11
ER -