Generating Bone Marrow Chimeric Mouse Using GPR120 Deficient Mouse for the Study of DHA Inhibitory Effect on Osteoclast Formation and Bone Resorption

被引:2
作者
Ma, Jinghan [1 ]
Kitaura, Hideki [1 ]
Ohori, Fumitoshi [1 ]
Noguchi, Takahiro [1 ]
Marahleh, Aseel [2 ]
Kinjo, Ria [1 ]
Kanou, Kayoko [1 ]
Ren, Jiayi [1 ]
Miura, Mariko [1 ]
Narita, Kohei [1 ]
Mizoguchi, Itaru [1 ]
机构
[1] Tohoku Univ, Grad Sch Dent, Div Orthodont & Dentofacial Orthoped, 4-1,Seiryo Machi,Aoba Ku, Sendai 9808575, Japan
[2] Tohoku Univ, Frontier Res Inst Interdisciplinary Sci, Sendai 9808575, Japan
关键词
DHA; chimeric mouse; GPR120; osteoclastogenesis; TNF-alpha; TUMOR-NECROSIS-FACTOR; DOCOSAHEXAENOIC ACID; RECEPTOR; TNF; ALPHA; DIFFERENTIATION; INFLAMMATION; OSTEOBLAST; MEDIATORS; ARTHRITIS;
D O I
10.3390/ijms242317000
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Docosahexaenoic acid (DHA) is an omega-3 fatty acid that exerts physiological effects via G protein-coupled receptor 120 (GPR120). In our previous studies, we figured out the inhibitory effects of DHA on TNF-alpha (Tumor necrosis factor-alpha)-induced osteoclastogenesis via GPR120 in vivo. Moreover, DHA directly suppressed RANKL expression in osteoblasts via GPR120 in vitro. In this study, we generated bone marrow chimeric mice using GPR120 deficient mice (GPR120-KO) to study the inhibitory effects of DHA on bone resorption and osteoclast formation. Bone marrow cells of wild-type (WT) or GPR120-KO mice were transplanted into irradiated recipient mice, which were WT or GPR120 deficient mice. The resulting chimeric mice contained stromal cells from the recipient and bone marrow cells, including osteoclast precursors, from the donor. These chimeric mice were used to perform a series of histological and microfocus computed tomography (micro-CT) analyses after TNF-alpha injection for induction of osteoclast formation with or without DHA. Osteoclast number and bone resorption were found to be significantly increased in chimeric mice, which did not express GPR120 in stromal cells, compared to chimeric mice, which expressed GPR120 in stromal cells. DHA was also found to suppress specific signaling pathways. We summarized that DHA suppressed TNF-alpha-induced stromal-dependent osteoclast formation and bone resorption via GPR120.
引用
收藏
页数:15
相关论文
共 49 条
[1]   A Review on the Use of Anti-TNF in Children and Adolescents with Inflammatory Bowel Disease [J].
Aardoom, Martine A. ;
Veereman, Gigi ;
de Ridder, Lissy .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (10)
[2]   Lipopolysaccharide- TLR-4 Axis regulates Osteoclastogenesis independent of RANKL/RANK signaling [J].
AlQranei, Mohammed S. ;
Senbanjo, Linda T. ;
Aljohani, Hanan ;
Hamza, Therwa ;
Chellaiah, Meenakshi A. .
BMC IMMUNOLOGY, 2021, 22 (01)
[3]  
Caetano-Lopes J, 2007, ACTA REUMATOL PORT, V32, P103
[4]   Osteoblast and osteocyte: Games without frontiers [J].
Capulli, Mattia ;
Paone, Riccardo ;
Rucci, Nadia .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2014, 561 :3-12
[5]   Omega-3 fatty acid-rich fish oil supplementation prevents rosiglitazone-induced osteopenia in aging C57BL/6 mice and in vitro studies [J].
Cugno, Chiara ;
Kizhakayil, Dhanya ;
Calzone, Rita ;
Rahman, Shaikh Mizanoor ;
Halade, Ganesh, V ;
Rahman, Md M. .
SCIENTIFIC REPORTS, 2021, 11 (01)
[6]   Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells [J].
Florencio-Silva, Rinaldo ;
da Silva Sasso, Gisela Rodrigues ;
Sasso-Cerri, Estela ;
Simoes, Manuel Jesus ;
Cerri, Paulo Sergio .
BIOMED RESEARCH INTERNATIONAL, 2015, 2015
[7]   The effect of fish oil supplementation on resistance training-induced adaptations [J].
Heileson, Jeffery L. ;
Machek, Steven B. ;
Harris, Dillon R. ;
Tomek, Sara ;
de Souza, Leticia C. ;
Kieffer, Adam J. ;
Barringer, Nicholas D. ;
Gallucci, Andrew ;
Forsse, Jeffrey S. ;
Funderburk, LesLee K. .
JOURNAL OF THE INTERNATIONAL SOCIETY OF SPORTS NUTRITION, 2023, 20 (01)
[8]   Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human [J].
Ichimura, Atsuhiko ;
Hirasawa, Akira ;
Poulain-Godefroy, Odile ;
Bonnefond, Amelie ;
Hara, Takafumi ;
Yengo, Loic ;
Kimura, Ikuo ;
Leloire, Audrey ;
Liu, Ning ;
Iida, Keiko ;
Choquet, Helene ;
Besnard, Philippe ;
Lecoeur, Cecile ;
Vivequin, Sidonie ;
Ayukawa, Kumiko ;
Takeuchi, Masato ;
Ozawa, Kentaro ;
Tauber, Maithe ;
Maffeis, Claudio ;
Morandi, Anita ;
Buzzetti, Raffaella ;
Elliott, Paul ;
Pouta, Anneli ;
Jarvelin, Marjo-Riitta ;
Koerner, Antje ;
Kiess, Wieland ;
Pigeyre, Marie ;
Caiazzo, Roberto ;
Van Hul, Wim ;
Van Gaal, Luc ;
Horber, Fritz ;
Balkau, Beverley ;
Levy-Marchal, Claire ;
Rouskas, Konstantinos ;
Kouvatsi, Anastasia ;
Hebebrand, Johannes ;
Hinney, Anke ;
Scherag, Andre ;
Pattou, Francois ;
Meyre, David ;
Koshimizu, Taka-aki ;
Wolowczuk, Isabelle ;
Tsujimoto, Gozoh ;
Froguel, Philippe .
NATURE, 2012, 483 (7389) :350-U149
[10]   Impact of GPCRs in clinical medicine: Monogenic diseases, genetic variants and drug targets [J].
Insel, Paul A. ;
Tang, Chih-Min ;
Hahntow, Ines ;
Michel, Martin C. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2007, 1768 (04) :994-1005