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
Hauptverfasser: 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
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container_issue 10
container_start_page 2766
container_title Autophagy
container_volume 17
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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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><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 &amp; 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 &amp; Francis Group 2020</rights><rights>2020 Informa UK Limited, trading as Taylor &amp; Francis Group 2020 Informa UK Limited, trading as Taylor &amp; 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 &amp; 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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.</abstract><cop>United States</cop><pub>Taylor &amp; 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>
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identifier ISSN: 1554-8627
ispartof Autophagy, 2021-10, Vol.17 (10), p.2766-2782
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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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