Skip to main content
Log in

Sirtuin 1 inhibits TNF-α-mediated osteoclastogenesis of bone marrow-derived macrophages through both ROS generation and TRPV1 activation

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

Sirtuin 1 (SIRT1), also known as NAD-dependent deacetylase, has been reported to increase in vivo osteoclast-mediated bone resorption. However, its effects on osteoclastogenesis or bone loss in vitro have not been widely examined. Therefore, the effects and underlying mechanism of SIRT1 on osteoclast differentiation in mice in vitro were studied. During RANKL-induced osteoclastogenesis in differentiated bone marrow-derived macrophages (BMMs), SIRT1 downregulation was observed. The use of resveratrol (SIRT1 activator) and SIRT1 overexpression was found to inhibit osteoclastogenesis, which was confirmed by TRAP staining and activity loss, reduced expression of osteoclast markers and related genes, and a decrease in the number of multinuclear cells. In contrast, treatment with EX-527 (SIRT1 inhibitor) as well as SIRT1 silencing promoted osteoclastogenesis. Furthermore, the tumor necrosis factor (TNF)-α level was reduced by resveratrol treatment and SIRT1 overexpression but increased following EX-527 incubation and SIRT1 depletion. TNF-α silencing blocked the osteoclastogenesis of BMMs promoted by SIRT1 depletion. Moreover, transient receptor potential vanilloid 1 (TRPV1) channel activation and reactive oxygen species (ROS) production, which are associated with osteoclastogenesis, were impaired by TNF-α silencing. These data demonstrate that SIRT1 directly inhibits osteoclastogenesis by inhibiting ROS generation and TRPV1 channel activation under mediation of TNF-α.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Lee SE, Chung WJ, Kwak HB, Chung CH, Kwack KB, Lee ZH, Kim HH (2001) Tumor necrosis factor-alpha supports the survival of osteoclasts through the activation of Akt and ERK. J Biol Chem 276(52):49343–49349. https://doi.org/10.1074/jbc.M103642200

    Article  CAS  PubMed  Google Scholar 

  2. Schwarz EM, Ritchlin CT (2007) Clinical development of anti-RANKL therapy. Arthritis Res Ther 9(1):S7. https://doi.org/10.1186/ar2171

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Teitelbaum SL (2000) Bone resorption by osteoclasts. Science 289(5484):1504–1508

    Article  CAS  PubMed  Google Scholar 

  4. Quinn JM, Horwood NJ, Elliott J, Gillespie MT, Martin TJ (2000) Fibroblastic stromal cells express receptor activator of NF-kappa B ligand and support osteoclast differentiation. J Bone Miner Res 15(8):1459–1466. https://doi.org/10.1359/jbmr.2000.15.8.1459

    Article  CAS  PubMed  Google Scholar 

  5. Ross FP (2000) RANKing the importance of measles virus in Paget’s disease. J Clin Invest 105(5):555–558. https://doi.org/10.1172/JCI9557

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. McHugh KP, Hodivala-Dilke K, Zheng MH, Namba N, Lam J, Novack D, Feng X, Ross FP, Hynes RO, Teitelbaum SL (2000) Mice lacking beta3 integrins are osteosclerotic because of dysfunctional osteoclasts. J Clin Invest 105(4):433–440. https://doi.org/10.1172/JCI8905

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Sudo T, Nishikawa S, Ogawa M, Kataoka H, Ohno N, Izawa A, Hayashi S, Nishikawa S (1995) Functional hierarchy of c-kit and c-fms in intramarrow production of CFU-M. Oncogene 11(12):2469–2476

    CAS  PubMed  Google Scholar 

  8. Azuma Y, Kaji K, Katogi R, Takeshita S, Kudo A (2000) Tumor necrosis factor-alpha induces differentiation of and bone resorption by osteoclasts. J Biol Chem 275(7):4858–4864

    Article  CAS  PubMed  Google Scholar 

  9. Feldmann M, Brennan FM, Elliott MJ, Williams RO, Maini RN (1995) TNF alpha is an effective therapeutic target for rheumatoid arthritis. Ann N Y Acad Sci 766:272–278

    Article  CAS  PubMed  Google Scholar 

  10. Gravallese EM, Manning C, Tsay A, Naito A, Pan C, Amento E, Goldring SR (2000) Synovial tissue in rheumatoid arthritis is a source of osteoclast differentiation factor. Arthritis Rheum 43 (2):250–258. https://doi.org/10.1002/1529-0131(200002)43:2%3C250::Aid-anr3%3E3.0.Co;2-p

    Article  CAS  PubMed  Google Scholar 

  11. Takayanagi H, Iizuka H, Juji T, Nakagawa T, Yamamoto A, Miyazaki T, Koshihara Y, Oda H, Nakamura K, Tanaka S (2000) Involvement of receptor activator of nuclear factor kappaB ligand/osteoclast differentiation factor in osteoclastogenesis from synoviocytes in rheumatoid arthritis. Arthritis Rheum 43 (2):259–269. https://doi.org/10.1002/1529-0131(200002)43:2%3C259::Aid-anr4%3E3.0.Co;2-w

    Article  CAS  PubMed  Google Scholar 

  12. Harris WH (1995) The problem is osteolysis. Clin Orthop Relat Res 311:46–53

    Google Scholar 

  13. Jiranek WA, Machado M, Jasty M, Jevsevar D, Wolfe HJ, Goldring SR, Goldberg MJ, Harris WH (1993) Production of cytokines around loosened cemented acetabular components. Analysis with immunohistochemical techniques and in situ hybridization. J Bone Joint Surg Am 75(6):863–879

    Article  CAS  PubMed  Google Scholar 

  14. Duff GW (1994) Cytokines and acute phase proteins in rheumatoid arthritis. Scand J Rheumatol Suppl 100:9–19

    Article  CAS  PubMed  Google Scholar 

  15. Ulfgren AK, Lindblad S, Klareskog L, Andersson J, Andersson U (1995) Detection of cytokine producing cells in the synovial membrane from patients with rheumatoid arthritis. Ann Rheum Dis 54(8):654–661

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Allen JE, Maizels RM (1997) Th1-Th2: reliable paradigm or dangerous dogma? Immunol Today 18(8):387–392

    Article  CAS  PubMed  Google Scholar 

  17. Sebastian C, Satterstrom FK, Haigis MC, Mostoslavsky R (2012) From sirtuin biology to human diseases: an update. J Biol Chem 287(51):42444–42452. https://doi.org/10.1074/jbc.R112.402768

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Herranz D, Munoz-Martin M, Canamero M, Mulero F, Martinez-Pastor B, Fernandez-Capetillo O, Serrano M (2010) Sirt1 improves healthy ageing and protects from metabolic syndrome-associated cancer. Nat Commun 1:3. https://doi.org/10.1038/ncomms1001

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Cohen-Kfir E, Artsi H, Levin A, Abramowitz E, Bajayo A, Gurt I, Zhong L, D’Urso A, Toiber D, Mostoslavsky R, Dresner-Pollak R (2011) Sirt1 is a regulator of bone mass and a repressor of Sost encoding for sclerostin, a bone formation inhibitor. Endocrinology 152(12):4514–4524. https://doi.org/10.1210/en.2011-1128

    Article  CAS  PubMed  Google Scholar 

  20. Simic P, Zainabadi K, Bell E, Sykes DB, Saez B, Lotinun S, Baron R, Scadden D, Schipani E, Guarente L (2013) SIRT1 regulates differentiation of mesenchymal stem cells by deacetylating beta-catenin. EMBO Mol Med 5(3):430–440. https://doi.org/10.1002/emmm.201201606

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Iyer S, Han L, Bartell SM, Kim HN, Gubrij I, de Cabo R, O’Brien CA, Manolagas SC, Almeida M (2014) Sirtuin1 (Sirt1) promotes cortical bone formation by preventing beta-catenin sequestration by FoxO transcription factors in osteoblast progenitors. J Biol Chem 289(35):24069–24078. https://doi.org/10.1074/jbc.M114.561803

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Edwards JR, Perrien DS, Fleming N, Nyman JS, Ono K, Connelly L, Moore MM, Lwin ST, Yull FE, Mundy GR, Elefteriou F (2013) Silent information regulator (Sir)T1 inhibits NF-kappaB signaling to maintain normal skeletal remodeling. J Bone Miner Res 28(4):960–969. https://doi.org/10.1002/jbmr.1824

    Article  CAS  PubMed  Google Scholar 

  23. Gurt I, Artsi H, Cohen-Kfir E, Hamdani G, Ben-Shalom G, Feinstein B, El-Haj M, Dresner-Pollak R (2015) The Sirt1 activators SRT2183 and SRT3025 inhibit RANKL-induced osteoclastogenesis in bone marrow-derived macrophages and down-regulate Sirt3 in Sirt1 null cells. PLoS ONE 10(7):e0134391. https://doi.org/10.1371/journal.pone.0134391

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. He X, Andersson G, Lindgren U, Li Y (2010) Resveratrol prevents RANKL-induced osteoclast differentiation of murine osteoclast progenitor RAW 264.7 cells through inhibition of ROS production. Biochem Biophys Res Commun 401(3):356–362. https://doi.org/10.1016/j.bbrc.2010.09.053

    Article  CAS  PubMed  Google Scholar 

  25. Lee NK, Choi YG, Baik JY, Han SY, Jeong DW, Bae YS, Kim N, Lee SY (2005) A crucial role for reactive oxygen species in RANKL-induced osteoclast differentiation. Blood 106(3):852–859. https://doi.org/10.1182/blood-2004-09-3662

    Article  CAS  PubMed  Google Scholar 

  26. Srinivasan S, Koenigstein A, Joseph J, Sun L, Kalyanaraman B, Zaidi M, Avadhani NG (2010) Role of mitochondrial reactive oxygen species in osteoclast differentiation. Ann N Y Acad Sci 1192:245–252. https://doi.org/10.1111/j.1749-6632.2009.05377.x

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Idris AI, Landao-Bassonga E, Ralston SH (2010) The TRPV1 ion channel antagonist capsazepine inhibits osteoclast and osteoblast differentiation in vitro and ovariectomy induced bone loss in vivo. Bone 46(4):1089–1099. https://doi.org/10.1016/j.bone.2010.01.368

    Article  CAS  PubMed  Google Scholar 

  28. Jilka RL, Hangoc G, Girasole G, Passeri G, Williams DC, Abrams JS, Boyce B, Broxmeyer H, Manolagas SC (1992) Increased osteoclast development after estrogen loss: mediation by interleukin-6. Science 257(5066):88–91

    Article  CAS  PubMed  Google Scholar 

  29. Kirstein B, Chambers TJ, Fuller K (2006) Secretion of tartrate-resistant acid phosphatase by osteoclasts correlates with resorptive behavior. J Cell Biochem 98(5):1085–1094. https://doi.org/10.1002/jcb.20835

    Article  CAS  PubMed  Google Scholar 

  30. Lam J, Takeshita S, Barker JE, Kanagawa O, Ross FP, Teitelbaum SL (2000) TNF-alpha induces osteoclastogenesis by direct stimulation of macrophages exposed to permissive levels of RANK ligand. J Clin Invest 106(12):1481–1488. https://doi.org/10.1172/JCI11176

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Shakibaei M, Buhrmann C, Mobasheri A (2011) Resveratrol-mediated SIRT-1 interactions with p300 modulate receptor activator of NF-kappaB ligand (RANKL) activation of NF-kappaB signaling and inhibit osteoclastogenesis in bone-derived cells. J Biol Chem 286(13):11492–11505. https://doi.org/10.1074/jbc.M110.198713

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Nakamura T, Imai Y, Matsumoto T, Sato S, Takeuchi K, Igarashi K, Harada Y, Azuma Y, Krust A, Yamamoto Y, Nishina H, Takeda S, Takayanagi H, Metzger D, Kanno J, Takaoka K, Martin TJ, Chambon P, Kato S (2007) Estrogen prevents bone loss via estrogen receptor alpha and induction of Fas ligand in osteoclasts. Cell 130(5):811–823. https://doi.org/10.1016/j.cell.2007.07.025

    Article  CAS  PubMed  Google Scholar 

  33. Bowers JL, Tyulmenkov VV, Jernigan SC, Klinge CM (2000) Resveratrol acts as a mixed agonist/antagonist for estrogen receptors alpha and beta. Endocrinology 141(10):3657–3667. https://doi.org/10.1210/endo.141.10.7721

    Article  CAS  PubMed  Google Scholar 

  34. Gertz M, Fischer F, Nguyen GTT, Lakshminarasimhan M, Schutkowski M, Weyand M, Steegborn C (2013) Ex-527 inhibits Sirtuins by exploiting their unique NAD+-dependent deacetylation mechanism. Proc Natl Acad Sci USA 110(30):E2772–E2781. https://doi.org/10.1073/pnas.1303628110

    Article  PubMed  Google Scholar 

  35. Morgan MJ, Liu ZG (2011) Crosstalk of reactive oxygen species and NF-kappaB signaling. Cell Res 21(1):103–115. https://doi.org/10.1038/cr.2010.178

    Article  CAS  PubMed  Google Scholar 

  36. Kim MS, Yang YM, Son A, Tian YS, Lee SI, Kang SW, Muallem S, Shin DM (2010) RANKL-mediated reactive oxygen species pathway that induces long lasting Ca2 + oscillations essential for osteoclastogenesis. J Biol Chem 285(10):6913–6921. https://doi.org/10.1074/jbc.M109.051557

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Guo A, Vulchanova L, Wang J, Li X, Elde R (1999) Immunocytochemical localization of the vanilloid receptor 1 (VR1): relationship to neuropeptides, the P2 × 3 purinoceptor and IB4 binding sites. Eur J Neurosci 11(3):946–958

    Article  CAS  PubMed  Google Scholar 

  38. Wang Y, Gao Y, Tian Q, Deng Q, Wang Y, Zhou T, Liu Q, Mei K, Wang Y, Liu H, Ma R, Ding Y, Rong W, Cheng J, Yao J, Xu TL, Zhu MX, Li Y (2018) TRPV1 SUMOylation regulates nociceptive signaling in models of inflammatory pain. Nat Commun 9(1):1529. https://doi.org/10.1038/s41467-018-03974-7

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Choi JY, Lee HY, Hur J, Kim KH, Kang JY, Rhee CK, Lee SY (2018) TRPV1 blocking alleviates airway inflammation and remodeling in a chronic asthma murine model. Allergy Asthma Immunol Res 10(3):216–224. https://doi.org/10.4168/aair.2018.10.3.216

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Zhou Y, Song T, Peng J, Zhou Z, Wei H, Zhou R, Jiang S, Peng J (2016) SIRT1 suppresses adipogenesis by activating Wnt/beta-catenin signaling in vivo and in vitro. Oncotarget 7(47):77707–77720. https://doi.org/10.18632/oncotarget.12774

    Article  PubMed  PubMed Central  Google Scholar 

  41. Lin Y, Shen J, Li D, Ming J, Liu X, Zhang N, Lai J, Shi M, Ji Q, Xing Y (2017) MiR-34a contributes to diabetes-related cochlear hair cell apoptosis via SIRT1/HIF-1alpha signaling. Gen Comp Endocrinol 246:63–70. https://doi.org/10.1016/j.ygcen.2017.02.017

    Article  CAS  PubMed  Google Scholar 

Download references

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Liangzhi Wang.

Ethics declarations

Conflict of interest

The authors declare that they have no conflicts of interest.

Ethical approval

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yan, S., Miao, L., Lu, Y. et al. Sirtuin 1 inhibits TNF-α-mediated osteoclastogenesis of bone marrow-derived macrophages through both ROS generation and TRPV1 activation. Mol Cell Biochem 455, 135–145 (2019). https://doi.org/10.1007/s11010-018-3477-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11010-018-3477-7

Keywords

Navigation