Autophagy receptor OPTN (optineurin) regulates mesenchymal stem cell fate and bone-fat balance during aging by clearing FABP3
Senile osteoporosis (OP) is often concomitant with decreased autophagic activity. OPTN (optineurin), a macroautophagy/autophagy (hereinafter referred to as autophagy) receptor, is found to play a pivotal role in selective autophagy, coupling autophagy with bone metabolism. However, its role in osteo...
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Veröffentlicht in: | Autophagy 2021-10, Vol.17 (10), p.2766-2782 |
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creator | Liu, Zheng-Zhao Hong, Chun-Gu Hu, Wen-Bao Chen, Meng-Lu Duan, Ran Li, Hong-Ming Yue, Tao Cao, Jia Wang, Zhen-Xing Chen, Chun-Yuan Hu, Xiong-Ke Wu, Ben Liu, Hao-Ming Tan, Yi-Juan Liu, Jiang-Hua Luo, Zhong-Wei Zhang, Yan Rao, Shan-Shan Luo, Ming-Jie Yin, Hao Wang, Yi-Yi Xia, Kun Xu, Lang Tang, Si-Yuan Hu, Rong-Gui Xie, Hui |
description | Senile osteoporosis (OP) is often concomitant with decreased autophagic activity. OPTN (optineurin), a macroautophagy/autophagy (hereinafter referred to as autophagy) receptor, is found to play a pivotal role in selective autophagy, coupling autophagy with bone metabolism. However, its role in osteogenesis is still mysterious. Herein, we identified Optn as a critical molecule of cell fate decision for bone marrow mesenchymal stem cells (MSCs), whose expression decreased in aged mice. Aged mice revealed osteoporotic bone loss, elevated senescence of MSCs, decreased osteogenesis, and enhanced adipogenesis, as well as optn
-
/ -
mice. Importantly, restoring Optn by transplanting wild-type MSCs to optn
-
/ -
mice or infecting optn
-
/ -
mice with Optn-containing lentivirus rescued bone loss. The introduction of a loss-of-function mutant of Optn
K193R
failed to reestablish a bone-fat balance. We further identified FABP3 (fatty acid binding protein 3, muscle and heart) as a novel selective autophagy substrate of OPTN. FABP3 promoted adipogenesis and inhibited osteogenesis of MSCs. Knockdown of FABP3 alleviated bone loss in optn
-
/ -
mice and aged mice. Our study revealed that reduced OPTN expression during aging might lead to OP due to a lack of FABP3 degradation via selective autophagy. FABP3 accumulation impaired osteogenesis of MSCs, leading to the occurrence of OP. Thus, reactivating OPTN or inhibiting FABP3 would open a new avenue to treat senile OP.
Abbreviations: ADIPOQ: adiponectin, C1Q and collagen domain containing; ALPL: alkaline phosphatase, liver/bone/kidney; BGLAP/OC/osteocalcin: bone gamma carboxyglutamate protein; BFR/BS: bone formation rate/bone surface; CALCOCO2/NDP52: calcium binding and coiled-coil domain 2; CDKN1A/p21: cyclin-dependent kinase inhibitor 1A; CDKN2A/p16: cyclin dependent kinase inhibitor 2A; CDKN2B/p15: cyclin dependent kinase inhibitor 2B; CEBPA: CCAAT/enhancer binding protein (C/EBP), alpha; COL1A1: collagen, type I, alpha 1; Ct. BV/TV: cortical bone volume fraction; Ct. Th: cortical thickness; Es. Pm: endocortical perimeter; FABP4/Ap2: fatty acid binding protein 4, adipocyte; H2AX: H2A.X variant histone; HE: hematoxylin and eosin; MAP1LC3B: microtubule-associated protein 1 light chain 3 beta; MAR: mineral apposition rate; MSCs: bone marrow mesenchymal stem cells; NBR1: NBR1, autophagy cargo receptor; OP: osteoporosis; OPTN: optineurin; PDB: Paget disease of bone; PPARG: peroxisome proliferator activated receptor gamma; Ps. |
doi_str_mv | 10.1080/15548627.2020.1839286 |
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-
/ -
mice. Importantly, restoring Optn by transplanting wild-type MSCs to optn
-
/ -
mice or infecting optn
-
/ -
mice with Optn-containing lentivirus rescued bone loss. The introduction of a loss-of-function mutant of Optn
K193R
failed to reestablish a bone-fat balance. We further identified FABP3 (fatty acid binding protein 3, muscle and heart) as a novel selective autophagy substrate of OPTN. FABP3 promoted adipogenesis and inhibited osteogenesis of MSCs. Knockdown of FABP3 alleviated bone loss in optn
-
/ -
mice and aged mice. Our study revealed that reduced OPTN expression during aging might lead to OP due to a lack of FABP3 degradation via selective autophagy. FABP3 accumulation impaired osteogenesis of MSCs, leading to the occurrence of OP. Thus, reactivating OPTN or inhibiting FABP3 would open a new avenue to treat senile OP.
Abbreviations: ADIPOQ: adiponectin, C1Q and collagen domain containing; ALPL: alkaline phosphatase, liver/bone/kidney; BGLAP/OC/osteocalcin: bone gamma carboxyglutamate protein; BFR/BS: bone formation rate/bone surface; CALCOCO2/NDP52: calcium binding and coiled-coil domain 2; CDKN1A/p21: cyclin-dependent kinase inhibitor 1A; CDKN2A/p16: cyclin dependent kinase inhibitor 2A; CDKN2B/p15: cyclin dependent kinase inhibitor 2B; CEBPA: CCAAT/enhancer binding protein (C/EBP), alpha; COL1A1: collagen, type I, alpha 1; Ct. BV/TV: cortical bone volume fraction; Ct. Th: cortical thickness; Es. Pm: endocortical perimeter; FABP4/Ap2: fatty acid binding protein 4, adipocyte; H2AX: H2A.X variant histone; HE: hematoxylin and eosin; MAP1LC3B: microtubule-associated protein 1 light chain 3 beta; MAR: mineral apposition rate; MSCs: bone marrow mesenchymal stem cells; NBR1: NBR1, autophagy cargo receptor; OP: osteoporosis; OPTN: optineurin; PDB: Paget disease of bone; PPARG: peroxisome proliferator activated receptor gamma; Ps. Pm: periosteal perimeter; qRT-PCR: quantitative real-time PCR; γH2AX: Phosphorylation of the Serine residue of H2AX; ROS: reactive oxygen species; RUNX2: runt related transcription factor 2; SA-GLB1: senescence-associated (SA)-GLB1 (galactosidase, beta 1); SP7/Osx/Osterix: Sp7 transcription factor 7; SQSTM1/p62: sequestosome 1; TAX1BP1: Tax1 (human T cell leukemia virus type I) binding protein 1; Tb. BV/TV: trabecular bone volume fraction; Tb. N: trabecular number; Tb. Sp: trabecular separation; Tb. Th: trabecular thickness; μCT: micro computed tomography.</description><identifier>ISSN: 1554-8627</identifier><identifier>EISSN: 1554-8635</identifier><identifier>DOI: 10.1080/15548627.2020.1839286</identifier><identifier>PMID: 33143524</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Adipogenesis ; Aging ; Animals ; Autophagy ; bone metabolism ; Cell Cycle Proteins - metabolism ; Cell Differentiation ; fabp3 ; Fatty Acid Binding Protein 3 - metabolism ; Membrane Transport Proteins - metabolism ; mesenchymal stem cell ; Mesenchymal Stem Cells - metabolism ; Mice ; optineurin ; Osteogenesis ; Osteoporosis ; Research Paper ; senescence ; X-Ray Microtomography</subject><ispartof>Autophagy, 2021-10, Vol.17 (10), p.2766-2782</ispartof><rights>2020 Informa UK Limited, trading as Taylor & Francis Group 2020</rights><rights>2020 Informa UK Limited, trading as Taylor & Francis Group 2020 Informa UK Limited, trading as Taylor & Francis Group</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-781db0eeb7a03735b597b88afe92c2ba9f99442f73486474eb47bd2961bbab213</citedby><cites>FETCH-LOGICAL-c468t-781db0eeb7a03735b597b88afe92c2ba9f99442f73486474eb47bd2961bbab213</cites><orcidid>0000-0003-4250-7152</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526045/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526045/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33143524$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Zheng-Zhao</creatorcontrib><creatorcontrib>Hong, Chun-Gu</creatorcontrib><creatorcontrib>Hu, Wen-Bao</creatorcontrib><creatorcontrib>Chen, Meng-Lu</creatorcontrib><creatorcontrib>Duan, Ran</creatorcontrib><creatorcontrib>Li, Hong-Ming</creatorcontrib><creatorcontrib>Yue, Tao</creatorcontrib><creatorcontrib>Cao, Jia</creatorcontrib><creatorcontrib>Wang, Zhen-Xing</creatorcontrib><creatorcontrib>Chen, Chun-Yuan</creatorcontrib><creatorcontrib>Hu, Xiong-Ke</creatorcontrib><creatorcontrib>Wu, Ben</creatorcontrib><creatorcontrib>Liu, Hao-Ming</creatorcontrib><creatorcontrib>Tan, Yi-Juan</creatorcontrib><creatorcontrib>Liu, Jiang-Hua</creatorcontrib><creatorcontrib>Luo, Zhong-Wei</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Rao, Shan-Shan</creatorcontrib><creatorcontrib>Luo, Ming-Jie</creatorcontrib><creatorcontrib>Yin, Hao</creatorcontrib><creatorcontrib>Wang, Yi-Yi</creatorcontrib><creatorcontrib>Xia, Kun</creatorcontrib><creatorcontrib>Xu, Lang</creatorcontrib><creatorcontrib>Tang, Si-Yuan</creatorcontrib><creatorcontrib>Hu, Rong-Gui</creatorcontrib><creatorcontrib>Xie, Hui</creatorcontrib><title>Autophagy receptor OPTN (optineurin) regulates mesenchymal stem cell fate and bone-fat balance during aging by clearing FABP3</title><title>Autophagy</title><addtitle>Autophagy</addtitle><description>Senile osteoporosis (OP) is often concomitant with decreased autophagic activity. OPTN (optineurin), a macroautophagy/autophagy (hereinafter referred to as autophagy) receptor, is found to play a pivotal role in selective autophagy, coupling autophagy with bone metabolism. However, its role in osteogenesis is still mysterious. Herein, we identified Optn as a critical molecule of cell fate decision for bone marrow mesenchymal stem cells (MSCs), whose expression decreased in aged mice. Aged mice revealed osteoporotic bone loss, elevated senescence of MSCs, decreased osteogenesis, and enhanced adipogenesis, as well as optn
-
/ -
mice. Importantly, restoring Optn by transplanting wild-type MSCs to optn
-
/ -
mice or infecting optn
-
/ -
mice with Optn-containing lentivirus rescued bone loss. The introduction of a loss-of-function mutant of Optn
K193R
failed to reestablish a bone-fat balance. We further identified FABP3 (fatty acid binding protein 3, muscle and heart) as a novel selective autophagy substrate of OPTN. FABP3 promoted adipogenesis and inhibited osteogenesis of MSCs. Knockdown of FABP3 alleviated bone loss in optn
-
/ -
mice and aged mice. Our study revealed that reduced OPTN expression during aging might lead to OP due to a lack of FABP3 degradation via selective autophagy. FABP3 accumulation impaired osteogenesis of MSCs, leading to the occurrence of OP. Thus, reactivating OPTN or inhibiting FABP3 would open a new avenue to treat senile OP.
Abbreviations: ADIPOQ: adiponectin, C1Q and collagen domain containing; ALPL: alkaline phosphatase, liver/bone/kidney; BGLAP/OC/osteocalcin: bone gamma carboxyglutamate protein; BFR/BS: bone formation rate/bone surface; CALCOCO2/NDP52: calcium binding and coiled-coil domain 2; CDKN1A/p21: cyclin-dependent kinase inhibitor 1A; CDKN2A/p16: cyclin dependent kinase inhibitor 2A; CDKN2B/p15: cyclin dependent kinase inhibitor 2B; CEBPA: CCAAT/enhancer binding protein (C/EBP), alpha; COL1A1: collagen, type I, alpha 1; Ct. BV/TV: cortical bone volume fraction; Ct. Th: cortical thickness; Es. Pm: endocortical perimeter; FABP4/Ap2: fatty acid binding protein 4, adipocyte; H2AX: H2A.X variant histone; HE: hematoxylin and eosin; MAP1LC3B: microtubule-associated protein 1 light chain 3 beta; MAR: mineral apposition rate; MSCs: bone marrow mesenchymal stem cells; NBR1: NBR1, autophagy cargo receptor; OP: osteoporosis; OPTN: optineurin; PDB: Paget disease of bone; PPARG: peroxisome proliferator activated receptor gamma; Ps. Pm: periosteal perimeter; qRT-PCR: quantitative real-time PCR; γH2AX: Phosphorylation of the Serine residue of H2AX; ROS: reactive oxygen species; RUNX2: runt related transcription factor 2; SA-GLB1: senescence-associated (SA)-GLB1 (galactosidase, beta 1); SP7/Osx/Osterix: Sp7 transcription factor 7; SQSTM1/p62: sequestosome 1; TAX1BP1: Tax1 (human T cell leukemia virus type I) binding protein 1; Tb. BV/TV: trabecular bone volume fraction; Tb. N: trabecular number; Tb. Sp: trabecular separation; Tb. Th: trabecular thickness; μCT: micro computed tomography.</description><subject>Adipogenesis</subject><subject>Aging</subject><subject>Animals</subject><subject>Autophagy</subject><subject>bone metabolism</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell Differentiation</subject><subject>fabp3</subject><subject>Fatty Acid Binding Protein 3 - metabolism</subject><subject>Membrane Transport Proteins - metabolism</subject><subject>mesenchymal stem cell</subject><subject>Mesenchymal Stem Cells - metabolism</subject><subject>Mice</subject><subject>optineurin</subject><subject>Osteogenesis</subject><subject>Osteoporosis</subject><subject>Research Paper</subject><subject>senescence</subject><subject>X-Ray Microtomography</subject><issn>1554-8627</issn><issn>1554-8635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU1v1DAUjBCIlsJPAPlYDimOP2LnglgqCkgV7aGcrefkJRvk2IudFOXAfyfpbldw4eKPmXnz7DdZ9rqgFwXV9F0hpdAlUxeMsgXSvGK6fJKdrniuSy6fHs9MnWQvUvpBKS91xZ5nJ5wXgksmTrPfm2kMuy10M4lY424Mkdzc3n0j52E39h6n2Pu3C9VNDkZMZMCEvt7OAziSRhxIjc6RduEI-IbY4DFfbsSCA18jaVaDjkC3rnYmtUN4QK42H2_5y-xZCy7hq8N-ln2_-nR3-SW_vvn89XJzndei1GOudNFYimgVUK64tLJSVmtosWI1s1C1VSUEaxVfRiKUQCuUbVhVFtaCZQU_y97vfXeTHbCp0Y8RnNnFfoA4mwC9-Zfx_dZ04d5oyUoq5GJwfjCI4eeEaTRDn9avg8cwJcOEVKXW7KGX3EvrGFKK2B7bFNSs0ZnH6MwanTlEt9S9-fuNx6rHrBbBh72g922IA_wK0TVmhNmF2MZl2n0y_P89_gAMT6pf</recordid><startdate>20211003</startdate><enddate>20211003</enddate><creator>Liu, Zheng-Zhao</creator><creator>Hong, Chun-Gu</creator><creator>Hu, Wen-Bao</creator><creator>Chen, Meng-Lu</creator><creator>Duan, Ran</creator><creator>Li, Hong-Ming</creator><creator>Yue, Tao</creator><creator>Cao, Jia</creator><creator>Wang, Zhen-Xing</creator><creator>Chen, Chun-Yuan</creator><creator>Hu, Xiong-Ke</creator><creator>Wu, Ben</creator><creator>Liu, Hao-Ming</creator><creator>Tan, Yi-Juan</creator><creator>Liu, Jiang-Hua</creator><creator>Luo, Zhong-Wei</creator><creator>Zhang, Yan</creator><creator>Rao, Shan-Shan</creator><creator>Luo, Ming-Jie</creator><creator>Yin, Hao</creator><creator>Wang, Yi-Yi</creator><creator>Xia, Kun</creator><creator>Xu, Lang</creator><creator>Tang, Si-Yuan</creator><creator>Hu, Rong-Gui</creator><creator>Xie, Hui</creator><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4250-7152</orcidid></search><sort><creationdate>20211003</creationdate><title>Autophagy receptor OPTN (optineurin) regulates mesenchymal stem cell fate and bone-fat balance during aging by clearing FABP3</title><author>Liu, Zheng-Zhao ; Hong, Chun-Gu ; Hu, Wen-Bao ; Chen, Meng-Lu ; Duan, Ran ; Li, Hong-Ming ; Yue, Tao ; Cao, Jia ; Wang, Zhen-Xing ; Chen, Chun-Yuan ; Hu, Xiong-Ke ; Wu, Ben ; Liu, Hao-Ming ; Tan, Yi-Juan ; Liu, Jiang-Hua ; Luo, Zhong-Wei ; Zhang, Yan ; Rao, Shan-Shan ; Luo, Ming-Jie ; Yin, Hao ; Wang, Yi-Yi ; Xia, Kun ; Xu, Lang ; Tang, Si-Yuan ; Hu, Rong-Gui ; Xie, Hui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-781db0eeb7a03735b597b88afe92c2ba9f99442f73486474eb47bd2961bbab213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adipogenesis</topic><topic>Aging</topic><topic>Animals</topic><topic>Autophagy</topic><topic>bone metabolism</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell Differentiation</topic><topic>fabp3</topic><topic>Fatty Acid Binding Protein 3 - metabolism</topic><topic>Membrane Transport Proteins - metabolism</topic><topic>mesenchymal stem cell</topic><topic>Mesenchymal Stem Cells - metabolism</topic><topic>Mice</topic><topic>optineurin</topic><topic>Osteogenesis</topic><topic>Osteoporosis</topic><topic>Research Paper</topic><topic>senescence</topic><topic>X-Ray Microtomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Zheng-Zhao</creatorcontrib><creatorcontrib>Hong, Chun-Gu</creatorcontrib><creatorcontrib>Hu, Wen-Bao</creatorcontrib><creatorcontrib>Chen, Meng-Lu</creatorcontrib><creatorcontrib>Duan, Ran</creatorcontrib><creatorcontrib>Li, Hong-Ming</creatorcontrib><creatorcontrib>Yue, Tao</creatorcontrib><creatorcontrib>Cao, Jia</creatorcontrib><creatorcontrib>Wang, Zhen-Xing</creatorcontrib><creatorcontrib>Chen, Chun-Yuan</creatorcontrib><creatorcontrib>Hu, Xiong-Ke</creatorcontrib><creatorcontrib>Wu, Ben</creatorcontrib><creatorcontrib>Liu, Hao-Ming</creatorcontrib><creatorcontrib>Tan, Yi-Juan</creatorcontrib><creatorcontrib>Liu, Jiang-Hua</creatorcontrib><creatorcontrib>Luo, Zhong-Wei</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Rao, Shan-Shan</creatorcontrib><creatorcontrib>Luo, Ming-Jie</creatorcontrib><creatorcontrib>Yin, Hao</creatorcontrib><creatorcontrib>Wang, Yi-Yi</creatorcontrib><creatorcontrib>Xia, Kun</creatorcontrib><creatorcontrib>Xu, Lang</creatorcontrib><creatorcontrib>Tang, Si-Yuan</creatorcontrib><creatorcontrib>Hu, Rong-Gui</creatorcontrib><creatorcontrib>Xie, Hui</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Autophagy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Zheng-Zhao</au><au>Hong, Chun-Gu</au><au>Hu, Wen-Bao</au><au>Chen, Meng-Lu</au><au>Duan, Ran</au><au>Li, Hong-Ming</au><au>Yue, Tao</au><au>Cao, Jia</au><au>Wang, Zhen-Xing</au><au>Chen, Chun-Yuan</au><au>Hu, Xiong-Ke</au><au>Wu, Ben</au><au>Liu, Hao-Ming</au><au>Tan, Yi-Juan</au><au>Liu, Jiang-Hua</au><au>Luo, Zhong-Wei</au><au>Zhang, Yan</au><au>Rao, Shan-Shan</au><au>Luo, Ming-Jie</au><au>Yin, Hao</au><au>Wang, Yi-Yi</au><au>Xia, Kun</au><au>Xu, Lang</au><au>Tang, Si-Yuan</au><au>Hu, Rong-Gui</au><au>Xie, Hui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autophagy receptor OPTN (optineurin) regulates mesenchymal stem cell fate and bone-fat balance during aging by clearing FABP3</atitle><jtitle>Autophagy</jtitle><addtitle>Autophagy</addtitle><date>2021-10-03</date><risdate>2021</risdate><volume>17</volume><issue>10</issue><spage>2766</spage><epage>2782</epage><pages>2766-2782</pages><issn>1554-8627</issn><eissn>1554-8635</eissn><abstract>Senile osteoporosis (OP) is often concomitant with decreased autophagic activity. OPTN (optineurin), a macroautophagy/autophagy (hereinafter referred to as autophagy) receptor, is found to play a pivotal role in selective autophagy, coupling autophagy with bone metabolism. However, its role in osteogenesis is still mysterious. Herein, we identified Optn as a critical molecule of cell fate decision for bone marrow mesenchymal stem cells (MSCs), whose expression decreased in aged mice. Aged mice revealed osteoporotic bone loss, elevated senescence of MSCs, decreased osteogenesis, and enhanced adipogenesis, as well as optn
-
/ -
mice. Importantly, restoring Optn by transplanting wild-type MSCs to optn
-
/ -
mice or infecting optn
-
/ -
mice with Optn-containing lentivirus rescued bone loss. The introduction of a loss-of-function mutant of Optn
K193R
failed to reestablish a bone-fat balance. We further identified FABP3 (fatty acid binding protein 3, muscle and heart) as a novel selective autophagy substrate of OPTN. FABP3 promoted adipogenesis and inhibited osteogenesis of MSCs. Knockdown of FABP3 alleviated bone loss in optn
-
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mice and aged mice. Our study revealed that reduced OPTN expression during aging might lead to OP due to a lack of FABP3 degradation via selective autophagy. FABP3 accumulation impaired osteogenesis of MSCs, leading to the occurrence of OP. Thus, reactivating OPTN or inhibiting FABP3 would open a new avenue to treat senile OP.
Abbreviations: ADIPOQ: adiponectin, C1Q and collagen domain containing; ALPL: alkaline phosphatase, liver/bone/kidney; BGLAP/OC/osteocalcin: bone gamma carboxyglutamate protein; BFR/BS: bone formation rate/bone surface; CALCOCO2/NDP52: calcium binding and coiled-coil domain 2; CDKN1A/p21: cyclin-dependent kinase inhibitor 1A; CDKN2A/p16: cyclin dependent kinase inhibitor 2A; CDKN2B/p15: cyclin dependent kinase inhibitor 2B; CEBPA: CCAAT/enhancer binding protein (C/EBP), alpha; COL1A1: collagen, type I, alpha 1; Ct. BV/TV: cortical bone volume fraction; Ct. Th: cortical thickness; Es. Pm: endocortical perimeter; FABP4/Ap2: fatty acid binding protein 4, adipocyte; H2AX: H2A.X variant histone; HE: hematoxylin and eosin; MAP1LC3B: microtubule-associated protein 1 light chain 3 beta; MAR: mineral apposition rate; MSCs: bone marrow mesenchymal stem cells; NBR1: NBR1, autophagy cargo receptor; OP: osteoporosis; OPTN: optineurin; PDB: Paget disease of bone; PPARG: peroxisome proliferator activated receptor gamma; Ps. Pm: periosteal perimeter; qRT-PCR: quantitative real-time PCR; γH2AX: Phosphorylation of the Serine residue of H2AX; ROS: reactive oxygen species; RUNX2: runt related transcription factor 2; SA-GLB1: senescence-associated (SA)-GLB1 (galactosidase, beta 1); SP7/Osx/Osterix: Sp7 transcription factor 7; SQSTM1/p62: sequestosome 1; TAX1BP1: Tax1 (human T cell leukemia virus type I) binding protein 1; Tb. BV/TV: trabecular bone volume fraction; Tb. N: trabecular number; Tb. Sp: trabecular separation; Tb. Th: trabecular thickness; μCT: micro computed tomography.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>33143524</pmid><doi>10.1080/15548627.2020.1839286</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-4250-7152</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1554-8627 |
ispartof | Autophagy, 2021-10, Vol.17 (10), p.2766-2782 |
issn | 1554-8627 1554-8635 |
language | eng |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Adipogenesis Aging Animals Autophagy bone metabolism Cell Cycle Proteins - metabolism Cell Differentiation fabp3 Fatty Acid Binding Protein 3 - metabolism Membrane Transport Proteins - metabolism mesenchymal stem cell Mesenchymal Stem Cells - metabolism Mice optineurin Osteogenesis Osteoporosis Research Paper senescence X-Ray Microtomography |
title | Autophagy receptor OPTN (optineurin) regulates mesenchymal stem cell fate and bone-fat balance during aging by clearing FABP3 |
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