PCLAF induces bone marrow adipocyte senescence and contributes to skeletal aging

Lingqi Xie , Yalun Cheng , Biao Hu , Xin Chen , Yuze An , Zhuying Xia , Guangping Cai , Changjun Li , Hui Peng

Bone Research ›› 2024, Vol. 12 ›› Issue (1) : 38

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Bone Research ›› 2024, Vol. 12 ›› Issue (1) : 38 DOI: 10.1038/s41413-024-00337-5
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PCLAF induces bone marrow adipocyte senescence and contributes to skeletal aging

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Abstract

Bone marrow adipocytes (BMAds) affect bone homeostasis, but the mechanism remains unclear. Here, we showed that exercise inhibited PCNA clamp-associated factor (PCLAF) secretion from the bone marrow macrophages to inhibit BMAds senescence and thus alleviated skeletal aging. The genetic deletion of PCLAF in macrophages inhibited BMAds senescence and delayed skeletal aging. In contrast, the transplantation of PCLAF-mediated senescent BMAds into the bone marrow of healthy mice suppressed bone turnover. Mechanistically, PCLAF bound to the ADGRL2 receptor to inhibit AKT/mTOR signaling that triggered BMAds senescence and subsequently spread senescence among osteogenic and osteoclastic cells. Of note, we developed a PCLAF-neutralizing antibody and showed its therapeutic effects on skeletal health in old mice. Together, these findings identify PCLAF as an inducer of BMAds senescence and provide a promising way to treat age-related osteoporosis.

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Lingqi Xie, Yalun Cheng, Biao Hu, Xin Chen, Yuze An, Zhuying Xia, Guangping Cai, Changjun Li, Hui Peng. PCLAF induces bone marrow adipocyte senescence and contributes to skeletal aging. Bone Research, 2024, 12(1): 38 DOI:10.1038/s41413-024-00337-5

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References

[1]

Hattner R, Epker BN, Frost HM. Suggested sequential mode of control of changes in cell behaviour in adult bone remodelling. Nature, 1965, 206: 489-490

[2]

Pietschmann P et al. Bone structure and metabolism in a rodent model of male senile osteoporosis. Exp. Gerontol., 2007, 42: 1099-1108

[3]

Feng X, McDonald JM. Disorders of bone remodeling. Annu. Rev. Pathol., 2011, 6: 121-145

[4]

Xie H et al. PDGF-BB secreted by preosteoclasts induces angiogenesis during coupling with osteogenesis. Nat. Med., 2014, 20: 1270-1278

[5]

Li CJ et al. Senescent immune cells release grancalcin to promote skeletal aging. Cell Metab., 2021, 33: 1957-1973.e1956

[6]

Namba T et al. Age-related changes in bone morphology, function, and cell populations in inbred C57BL/6N mice. Japanese J. Veterinary Res., 2019, 67: 313-317

[7]

Fatayerji D, Eastell R. Age-related changes in bone turnover in men. J. Bone Miner. Res., 1999, 14: 1203-1210

[8]

Aaron N, Costa S, Rosen CJ, Qiang L. The implications of bone marrow adipose tissue on inflammaging. Front. Endocrinol. (Lausanne), 2022, 13

[9]

Wang L, Zhang H, Wang S, Chen X, Su J. Bone marrow adipocytes: a critical player in the bone marrow microenvironment. Front. Cell Dev. Biol., 2021, 9

[10]

Sebo ZL et al. Bone marrow adiposity: basic and clinical implications. Endocr. Rev., 2019, 40: 1187-1206

[11]

Yu B et al. PGC-1 alpha controls skeletal stem cell fate and bone-fat balance in osteoporosis and skeletal aging by inducing TAZ. Cell Stem Cell, 2018, 23: 193-209.e5

[12]

Chen P et al. Scara3 regulates bone marrow mesenchymal stem cell fate switch between osteoblasts and adipocytes by promoting Foxo1. Cell Prolif., 2021, 54

[13]

Fan Y et al. Parathyroid hormone directs bone marrow mesenchymal cell fate. Cell Metab., 2017, 25: 661-672

[14]

Li CJ et al. MicroRNA-188 regulates age-related switch between osteoblast and adipocyte differentiation. J. Clin. Invest., 2015, 125: 1509-1522

[15]

Yang M et al. Krüppel-like factor 3 inhibition by mutated lncRNA Reg1cp results in human high bone mass syndrome. J. Exp. Med., 2019, 216: 1944-1964

[16]

Liu X et al. Oxylipin-PPARγ-initiated adipocyte senescence propagates secondary senescence in the bone marrow. Cell Metab., 2023, 35: 667-684.e666

[17]

Tong L, Chen D. Senescence of bone marrow fat cells: A new clue for glucocorticoid-induced bone deterioration. Cell Metab., 2023, 35: 551-553

[18]

Pagnotti GM et al. Combating osteoporosis and obesity with exercise: leveraging cell mechanosensitivity. Nat. Rev. Endocrinol., 2019, 15: 339-355

[19]

Dolan, E., Artioli, G. G., Pereira, R. M. R. & Gualano, B. Muscular atrophy and sarcopenia in the elderly: is there a role for creatine supplementation? Biomolecules 9, 642 (2019).

[20]

Bischoff-Ferrari HA et al. Effect of vitamin D supplementation, omega-3 fatty acid supplementation, or a strength-training exercise program on clinical outcomes in older adults: the do-health randomized clinical trial. JAMA, 2020, 324: 1855-1868

[21]

Dietlein N, Rodewald HR. Runner’s niche: multipurpose stromal cells maintained by exercise. Trends Immunol., 2021, 42: 841-843

[22]

Vico L, Hargens A. Skeletal changes during and after spaceflight. Nat. Rev. Rheumatol., 2018, 14: 229-245

[23]

Schafer MJ et al. Exercise prevents diet-induced cellular senescence in adipose tissue. Diabetes, 2016, 65: 1606-1615

[24]

Peng H et al. A mechanosensitive lipolytic factor in the bone marrow promotes osteogenesis and lymphopoiesis. Cell Metab., 2022, 34: 1168-1182.e1166

[25]

Little-Letsinger SE et al. Exercise to mend aged-tissue crosstalk in bone targeting osteoporosis & osteoarthritis. Semin. Cell Dev. Biol., 2022, 123: 22-35

[26]

Rendina-Ruedy E, Rosen CJ. Lipids in the bone marrow: an evolving perspective. Cell Metab., 2020, 31: 219-231

[27]

Styner M et al. Bone marrow fat accumulation accelerated by high fat diet is suppressed by exercise. Bone, 2014, 64: 39-46

[28]

Farr JN et al. Targeting cellular senescence prevents age-related bone loss in mice. Nat. Med., 2017, 23: 1072-1079

[29]

Khosla S, Farr JN, Tchkonia T, Kirkland JL. The role of cellular senescence in ageing and endocrine disease. Nat. Rev. Endocrinol., 2020, 16: 263-275

[30]

Ou MY, Zhang H, Tan PC, Zhou SB, Li QF. Adipose tissue aging: mechanisms and therapeutic implications. Cell Death Dis., 2022, 13

[31]

Liu LJ, Liao JM, Zhu F. Proliferating cell nuclear antigen clamp associated factor, a potential proto-oncogene with increased expression in malignant gastrointestinal tumors. World J. Gastrointest. Oncol., 2021, 13: 1425-1439

[32]

Emanuele MJ, Ciccia A, Elia AE, Elledge SJ. Proliferating cell nuclear antigen (PCNA)-associated KIAA0101/PAF15 protein is a cell cycle-regulated anaphase-promoting complex/cyclosome substrate. Proc. Natl. Acad. Sci. USA., 2011, 108: 9845-9850

[33]

Hosfield DJ, Mol CD, Shen B, Tainer JA. Structure of the DNA repair and replication endonuclease and exonuclease FEN-1: coupling DNA and PCNA binding to FEN-1 activity. Cell, 1998, 95: 135-146

[34]

Suchý T et al. The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance. Int. J. Obes. (Lond), 2020, 44: 2124-2136

[35]

Tikhonova AN et al. The bone marrow microenvironment at single-cell resolution. Nature, 2019, 569: 222-228

[36]

Ambrosi TH et al. Aged skeletal stem cells generate an inflammatory degenerative niche. Nature, 2021, 597: 256-262

[37]

Mitchell CA et al. Stromal niche inflammation mediated by IL-1 signalling is a targetable driver of haematopoietic ageing. Nat. Cell Biol., 2023, 25: 30-41

[38]

Li J et al. TGFβ1+ CCR5+ neutrophil subset increases in bone marrow and causes age-related osteoporosis in male mice. Nat. Commun., 2023, 14

[39]

Li J, Chen X, Lu L, Yu X. The relationship between bone marrow adipose tissue and bone metabolism in postmenopausal osteoporosis. Cytokine Growth Factor Rev., 2020, 52: 88-98

[40]

Schaum N et al. Ageing hallmarks exhibit organ-specific temporal signatures. Nature, 2020, 583: 596-602

[41]

Rosen ED, Spiegelman BM. What we talk about when we talk about fat. Cell, 2014, 156: 20-44

[42]

Gillet C et al. Osteonecrosis of the femoral head: lipotoxicity exacerbation in msc and modifications of the bone marrow fluid. Endocrinology, 2017, 158: 490-502

[43]

Al Saedi A, Goodman CA, Myers DE, Hayes A, Duque G. Rapamycin affects palmitate-induced lipotoxicity in osteoblasts by modulating apoptosis and autophagy. J. Gerontol. A Biol. Sci. Med. Sci., 2020, 75: 58-63

[44]

Yu B et al. Wnt4 signaling prevents skeletal aging and inflammation by inhibiting nuclear factor-κB. Nat. Med., 2014, 20: 1009-1017

[45]

Oikonomou EK, Antoniades C. The role of adipose tissue in cardiovascular health and disease. Nat. Rev. Cardiol., 2019, 16: 83-99

[46]

Grabner GF, Xie H, Schweiger M, Zechner R. Lipolysis: cellular mechanisms for lipid mobilization from fat stores. Nat. Metab., 2021, 3: 1445-1465

[47]

Chandra A et al. Targeted reduction of senescent cell burden alleviates focal radiotherapy-related bone loss. J. Bone Miner. Res., 2020, 35: 1119-1131

[48]

Kirkland JL, Tchkonia T. Senolytic drugs: from discovery to translation. J. Intern. Med., 2020, 288: 518-536

[49]

Wang L et al. Mechanical sensing protein PIEZO1 regulates bone homeostasis via osteoblast-osteoclast crosstalk. Nat. Commun., 2020, 11

[50]

Katz JN, Arant KR, Loeser RF. Diagnosis and treatment of hip and knee osteoarthritis: a review. JAMA, 2021, 325: 568-578

[51]

Cawthorn WP, Scheller EL, MacDougald OA. Adipose tissue stem cells: the great WAT hope. Trends Endocrinol. Metab., 2012, 23: 270-277

[52]

Sanchez-Gurmaches J, Guertin DA. Adipocytes arise from multiple lineages that are heterogeneously and dynamically distributed. Nat. Commun., 2014, 5

[53]

Peirce V, Carobbio S, Vidal-Puig A. The different shades of fat. Nature, 2014, 510: 76-83

[54]

Muruganandan S, Sinal CJ. The impact of bone marrow adipocytes on osteoblast and osteoclast differentiation. IUBMB Life, 2014, 66: 147-155

[55]

Ambrosi TH et al. Adipocyte accumulation in the bone marrow during obesity and aging impairs stem cell-based hematopoietic and bone regeneration. Cell Stem Cell, 2017, 20: 771-784.e776

[56]

Deepika, F., Bathina, S. & Armamento-Villareal, R. Novel adipokines and their role in bone metabolism: a narrative review. Biomedicines 11, 644 (2023).

[57]

Jin C et al. PCNA-associated factor P15(PAF), targeted by FOXM1, predicts poor prognosis in high-grade serous ovarian cancer patients. Int. J. Cancer, 2018, 143: 2973-2984

[58]

Johnson SC, Rabinovitch PS, Kaeberlein M. mTOR is a key modulator of ageing and age-related disease. Nature, 2013, 493: 338-345

[59]

Mossmann D, Park S, Hall MN. mTOR signalling and cellular metabolism are mutual determinants in cancer. Nat. Rev. Cancer, 2018, 18: 744-757

[60]

Hamann J et al. International union of basic and clinical pharmacology. xciv. adhesion G protein-coupled receptors. Pharmacol. Rev., 2015, 67: 338-367

[61]

Black DM, Rosen CJ. Clinical practice. Postmenopausal osteoporosis. N. Engl. J. Med., 2016, 374: 254-262

[62]

Neer RM et al. Effect of parathyroid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis. N. Engl. J. Med., 2001, 344: 1434-1441

[63]

Balani DH, Ono N, Kronenberg HM. Parathyroid hormone regulates fates of murine osteoblast precursors in vivo. J. Clin. Invest., 2017, 127: 3327-3338

[64]

Wu X et al. Inhibition of Sca-1-positive skeletal stem cell recruitment by alendronate blunts the anabolic effects of parathyroid hormone on bone remodeling. Cell Stem Cell, 2010, 7: 571-580

[65]

Qiu T et al. TGF-beta type II receptor phosphorylates PTH receptor to integrate bone remodelling signalling. Nat. Cell Biol., 2010, 12: 224-234

[66]

Li C-J et al. Long noncoding RNA Bmncr regulates mesenchymal stem cell fate during skeletal aging. J. Clin. Investig., 2018, 128: 5251-5266

[67]

Cao JJ et al. Aging impairs IGF-I receptor activation and induces skeletal resistance to IGF-I. J. Bone Miner. Res., 2007, 22: 1271-1279

[68]

Hoffman CM, Han J, Calvi LM. Impact of aging on bone, marrow and their interactions. Bone, 2019, 119: 1-7

[69]

Scheller EL et al. Region-specific variation in the properties of skeletal adipocytes reveals regulated and constitutive marrow adipose tissues. Nat. Commun., 2015, 6

[70]

Zhen G et al. Inhibition of TGF-β signaling in mesenchymal stem cells of subchondral bone attenuates osteoarthritis. Nat. Med., 2013, 19: 704-712

[71]

Dou C et al. Sialylation of TLR2 initiates osteoclast fusion. Bone Res., 2022, 10: 24

[72]

Perez-Riverol Y et al. The PRIDE database and related tools and resources in 2019: improving support for quantification data. Nucleic Acids Res., 2019, 47: D442-d450

Funding

National Natural Science Foundation of China (National Science Foundation of China)(82201746)

National Key R&D Program of China (2021YFC2501702) National Key Research and Development Plan (2022YFC3601900, 2022YFC3601901, 2022YFC3601902, 2022YFC3601903, 2022YFC3601904, and 2022YFC3601905)

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