Home Medicine Impacts and mechanisms of PM2.5 on bone
Article
Licensed
Unlicensed Requires Authentication

Impacts and mechanisms of PM2.5 on bone

  • Yuqing Tian ORCID logo , Yunpeng Hu , Xiaoli Hou and Faming Tian EMAIL logo
Published/Copyright: August 3, 2023

Abstract

Osteoporosis is a metabolic bone disease, which is characterized by a decreased bone mass and deterioration of bone microstructure, resulting in increased bone fragility and a higher risk of fracture. The main pathological process of osteoporosis is the dynamic imbalance between bone absorption and bone formation, which can be caused by various factors such as air pollution. Particulate matter (PM)2.5 refers to the fine particles in the atmosphere, which are small in volume and large in specific surface area. These particles are prone to carrying toxic substances and have negative effects on several extrapulmonary organs, including bones. In this review, we present relevant data from studies, which show that PM2.5 is associated with abnormal bone turnover and osteoporosis. PM2.5 may cause or aggravate bone loss by stimulating an inflammatory response, inducing oxidative damage, reducing estrogen efficiency by competitive binding to estrogen receptors, or endocrine disorder mediated by binding with aromatic hydrocarbon receptors, and affecting the synthesis of vitamin D to reduce calcium absorption. The cellular and molecular mechanisms involved in these processes are also summarized in this review.


Corresponding author: Faming Tian, MD, PhD, School of Public Health, North China University of Science and Technology, Bohai Road 21, Caofeidian Dis., Tangshan, 063210, China, Phone: +86 0315 8816230, E-mail:

Funding source: Youth Talent Support Program of Hebei Province

Award Identifier / Grant number: JI-2016-10

Funding source: Nation Nature Science Foundation of China

Award Identifier / Grant number: NSFC81874029

Funding source: Nature Science Foundation of Hebei Province

Award Identifier / Grant number: H2022209054

Funding source: Basic Scientific Research Funds Program of Universities in Hebei Province

Award Identifier / Grant number: JYG2021005

Funding source: Central Government-guided Local Science and Technology Development Foundation of Hebei Province

Award Identifier / Grant number: 226Z7709G

Acknowledgments

We thank Ellen Knapp, PhD, from Liwen Bianji (Edanz) (www.liwenbianji.cn/), for editing the English text of a draft of this manuscript.

  1. Ethical approval: Not applicable.

  2. Informed consent: Not applicable.

  3. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Competing interests: Authors state no conflict of interest.

  5. Research funding: Nation Nature Science Foundation of China (NSFC81874029); Nature Science Foundation of Hebei Province (H2020209266; H2022209054); Basic Scientific Research Funds Program of Universities in Hebei Province (JYG2021005); Central Government-guided Local Science and Technology Development Foundation of Hebei Province (226Z7709G); Youth Talent Support Program of Hebei Province (JI-2016-10).

References

1. Organization WH. Ambient (outdoor) air quality and health; 2018. Available from: https://www.who.int/news-room/fact-sheets/detail/ambient-(outdoor)-air-quality-and-health.Search in Google Scholar

2. Li, R, Zhou, R, Zhang, J. Function of PM2.5 in the pathogenesis of lung cancer and chronic airway inflammatory diseases. Oncol Lett 2018;15:7506–14. https://doi.org/10.3892/ol.2018.8355.Search in Google Scholar PubMed PubMed Central

3. Lim, SS, Vos, T, Flaxman, AD, Danaei, G, Shibuya, K, Adair-Rohani, H, et al.. A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet 2012;380:2224–60. https://doi.org/10.1016/s0140-6736(12)61766-8.Search in Google Scholar PubMed PubMed Central

4. Abplanalp, W, Haberzettl, P, Bhatnagar, A, Conklin, DJ, O’Toole, TE. Carnosine supplementation mitigates the deleterious effects of particulate matter exposure in mice. J Am Heart Assoc 2019;8:e013041. https://doi.org/10.1161/jaha.119.013041.Search in Google Scholar

5. Wang, C, Feng, L, Chen, K. The impact of ambient particulate matter on hospital outpatient visits for respiratory and circulatory system disease in an urban Chinese population. Sci Total Environ 2019;666:672–9. https://doi.org/10.1016/j.scitotenv.2019.02.256.Search in Google Scholar PubMed

6. Chiu, YC, Lin, YT, Hsia, YF, Jung, CR, Lo, YC, Chen, TM, et al.. Long-term exposure to fine particulate matter and osteoporotic fracture: a case-control study in Taiwan. Environ Res 2021;196:110888. https://doi.org/10.1016/j.envres.2021.110888.Search in Google Scholar PubMed

7. Liu, T, Jiang, Y, Hu, J, Li, Z, Guo, Y, Li, X, et al.. Association of ambient PM(1) with hospital admission and recurrence of stroke in China. Sci Total Environ 2022;828:154131. https://doi.org/10.1016/j.scitotenv.2022.154131.Search in Google Scholar PubMed

8. Guo, LC, Lv, Z, Ma, W, Xiao, J, Lin, H, He, G, et al.. Contribution of heavy metals in PM(2.5) to cardiovascular disease mortality risk, a case study in Guangzhou, China. Chemosphere 2022;297:134102. https://doi.org/10.1016/j.chemosphere.2022.134102.Search in Google Scholar PubMed

9. Tsai, SS, Chiu, YW, Weng, YH, Yang, CY. Association between fine particulate air pollution and the risk of death from lung cancer in Taiwan. J Toxicol Environ Health A 2022;85:431–8. https://doi.org/10.1080/15287394.2022.2040672.Search in Google Scholar PubMed

10. Calderón-Garcidueñas, L, Calderón-Garcidueñas, A, Torres-Jardón, R, Avila-Ramírez, J, Kulesza, RJ, Angiulli, AD. Air pollution and your brain: what do you need to know right now. Prim Health Care Res Dev 2015;16:329–45. https://doi.org/10.1017/s146342361400036x.Search in Google Scholar

11. Salari, N, Ghasemi, H, Mohammadi, L, Behzadi, MH, Rabieenia, E, Shohaimi, S, et al.. The global prevalence of osteoporosis in the world: a comprehensive systematic review and meta-analysis. J Orthop Surg Res 2021;16:609. https://doi.org/10.1186/s13018-021-02772-0.Search in Google Scholar PubMed PubMed Central

12. Wu, J, Guo, B, Guan, H, Mi, F, Xu, J, Basang, et al.. The association between long-term exposure to ambient air pollution and bone strength in China. J Clin Endocrinol Metab 2021;106:e5097-108. https://doi.org/10.1210/clinem/dgab462.Search in Google Scholar PubMed

13. Qiao, D, Pan, J, Chen, G, Xiang, H, Tu, R, Zhang, X, et al.. Long-term exposure to air pollution might increase prevalence of osteoporosis in Chinese rural population. Environ Res 2020;183:109264. https://doi.org/10.1016/j.envres.2020.109264.Search in Google Scholar PubMed

14. Yang, Y, Li, R, Cai, M, Wang, X, Li, H, Wu, Y, et al.. Ambient air pollution, bone mineral density and osteoporosis: results from a national population-based cohort study. Chemosphere 2023;310:136871. https://doi.org/10.1016/j.chemosphere.2022.136871.Search in Google Scholar PubMed

15. Yu, P, Xu, R, Li, S, Coelho, M, Saldiva, PHN, Sim, MR, et al.. Associations between long-term exposure to PM(2.5) and site-specific cancer mortality: a nationwide study in Brazil between 2010 and 2018. Environ Pollut 2022;302:119070. https://doi.org/10.1016/j.envpol.2022.119070.Search in Google Scholar PubMed

16. Prada, D, Zhong, J, Colicino, E, Zanobetti, A, Schwartz, J, Dagincourt, N, et al.. Association of air particulate pollution with bone loss over time and bone fracture risk: analysis of data from two independent studies. Lancet Planet Health 2017;1:e337–47. https://doi.org/10.1016/s2542-5196(17)30136-5.Search in Google Scholar

17. Alvaer, K, Meyer, HE, Falch, JA, Nafstad, P, Søgaard, AJ. Outdoor air pollution and bone mineral density in elderly men – the Oslo Health Study. Osteoporos Int 2007;18:1669–74. https://doi.org/10.1007/s00198-007-0424-y.Search in Google Scholar PubMed

18. Adami, G, Cattani, G, Rossini, M, Viapiana, O, Olivi, P, Orsolini, G, et al.. Association between exposure to fine particulate matter and osteoporosis: a population-based cohort study. Osteoporos Int 2022;33:169–76. https://doi.org/10.1007/s00198-021-06060-9.Search in Google Scholar PubMed PubMed Central

19. Zhang, F, Zhou, F, Liu, H, Zhang, X, Zhu, S, Zhang, X, et al.. Long-term exposure to air pollution might decrease bone mineral density T-score and increase the prevalence of osteoporosis in Hubei province: evidence from China Osteoporosis Prevalence Study. Osteoporos Int 2022;33:2357–68. https://doi.org/10.1007/s00198-022-06488-7.Search in Google Scholar PubMed

20. Sieberath, A, Della Bella, E, Ferreira, AM, Gentile, P, Eglin, D, Dalgarno, K. A comparison of osteoblast and osteoclast in vitro Co-culture models and their translation for preclinical. Drug Test Appl 2020;21:912. https://doi.org/10.3390/ijms21030912.Search in Google Scholar PubMed PubMed Central

21. Chan, CK, Mason, A, Cooper, C, Dennison, E. Novel advances in the treatment of osteoporosis. Br Med Bull 2016;119:129–42. https://doi.org/10.1093/bmb/ldw033.Search in Google Scholar PubMed PubMed Central

22. Lv, YJ, Song, J, Xiong, LL, Huang, R, Zhu, P, Wang, P, et al.. Association of environmental cadmium exposure and bone remodeling in women over 50 years of age. Ecotoxicol Environ Saf 2021;211:111897. https://doi.org/10.1016/j.ecoenv.2021.111897.Search in Google Scholar PubMed

23. Ma, Y, Ran, D, Zhao, H, Song, R, Zou, H, Gu, J, et al.. Cadmium exposure triggers osteoporosis in duck via P2X7/PI3K/AKT-mediated osteoblast and osteoclast differentiation. Sci Total Environ 2021;750:141638. https://doi.org/10.1016/j.scitotenv.2020.141638.Search in Google Scholar PubMed

24. Hattori, T, Fei, W, Kizawa, T, Nishida, S, Yoshikawa, H, Kishida, Y. The fixed herbal drug composition “Saikokaryukotsuboreito” prevents bone loss with an association of serum IL-6 reductions in ovariectomized mice model. Phytomedicine 2010;17:170–7. https://doi.org/10.1016/j.phymed.2009.12.004.Search in Google Scholar PubMed

25. Calderón-Garcidueñas, L, Mora-Tiscareño, A, Francolira, M, Torres-Jardón, R, Peña-Cruz, B, Palacios-López, C, et al.. Exposure to urban air pollution and bone health in clinically healthy six-year-old children. Arh Hig Rad Toksikol 2013;64:23–34. https://doi.org/10.2478/10004-1254-64-2013-2219.Search in Google Scholar PubMed

26. Fujii, T, Hayashi, S, Hogg, JC, Mukae, H, Suwa, T, Goto, Y, et al.. Interaction of alveolar macrophages and airway epithelial cells following exposure to particulate matter produces mediators that stimulate the bone marrow. Am J Respir Cell Mol Biol 2002;27:34–41. https://doi.org/10.1165/ajrcmb.27.1.4787.Search in Google Scholar PubMed

27. Tan, WC, Qiu, D, Liam, BL, Ng, TP, Lee, SH, van Eeden, SF, et al.. The human bone marrow response to acute air pollution caused by forest fires. Am J Respir Crit Care Med 2000;161:1213–7. https://doi.org/10.1164/ajrccm.161.4.9904084.Search in Google Scholar PubMed

28. Han, B, Xu, J, Zhang, Y, Li, P, Li, K, Zhang, N, et al.. Associations of exposure to fine particulate matter mass and constituents with systemic inflammation: a cross-sectional study of urban older adults in China. Environ Sci Technol 2022;56:7244–55. https://doi.org/10.1021/acs.est.1c04488.Search in Google Scholar PubMed

29. Abu-Elmagd, M, Alghamdi, MA, Shamy, M, Khoder, MI, Costa, M, Assidi, M, et al.. Evaluation of the effects of airborne particulate matter on bone marrow-mesenchymal stem cells (BM-MSCs): cellular, molecular and systems biological approaches. Int J Environ Res Publ Health 2017;14:440. https://doi.org/10.3390/ijerph14040440.Search in Google Scholar PubMed PubMed Central

30. Giannoni, P, Marini, C, Cutrona, G, Matis, S, Capra, MC, Puglisi, F, et al.. Chronic lymphocytic leukemia cells impair osteoblastogenesis and promote osteoclastogenesis: role of TNFα, IL-6 and IL-11 cytokines. Haematologica 2021;106:2598–612. https://doi.org/10.3324/haematol.2019.231456.Search in Google Scholar PubMed PubMed Central

31. Ebe, Y, Nakamura, T. Effect of interleukin-1β on bone morphogenetic protein-9-induced osteoblastic differentiation of human periodontal ligament fibroblasts. Eur J Oral Sci 2021;129:e12792. https://doi.org/10.1111/eos.12792.Search in Google Scholar PubMed

32. Feng, W, Liu, H, Luo, T, Liu, D, Du, J, Sun, J, et al.. Combination of IL-6 and sIL-6R differentially regulate varying levels of RANKL-induced osteoclastogenesis through NF-κB, ERK and JNK signaling pathways. Sci Rep 2017;7:41411. https://doi.org/10.1038/srep41411.Search in Google Scholar PubMed PubMed Central

33. Yamashita, T, Yao, Z, Li, F, Zhang, Q, Badell, IR, Schwarz, EM, et al.. NF-kappaB p50 and p52 regulate receptor activator of NF-kappaB ligand (RANKL) and tumor necrosis factor-induced osteoclast precursor differentiation by activating c-Fos and NFATc1. J Biol Chem 2007;282:18245–53. https://doi.org/10.1074/jbc.m610701200.Search in Google Scholar

34. O’Brien, W, Fissel, BM, Maeda, Y, Yan, J, Ge, X, Gravallese, EM, et al.. RANK-independent osteoclast formation and bone erosion in inflammatory arthritis. Arthritis Rheumatol 2016;68:2889–900. https://doi.org/10.1002/art.39837.Search in Google Scholar PubMed PubMed Central

35. Song, L, Tan, J, Wang, Z, Ding, P, Tang, Q, Xia, M, et al.. Interleukin-17A facilitates osteoclast differentiation and bone resorption via activation of autophagy in mouse bone marrow macrophages. Mol Med Rep 2019;19:4743–52. https://doi.org/10.3892/mmr.2019.10155.Search in Google Scholar PubMed PubMed Central

36. Wells, A, Romberger, DJ, Thiele, GM, Wyatt, TA, Staab, E, Heires, AJ, et al.. Systemic IL-6 effector response in mediating systemic bone loss following inhalation of organic dust. J Interferon Cytokine Res 2017;37:9–19. https://doi.org/10.1089/jir.2016.0048.Search in Google Scholar PubMed PubMed Central

37. Valavanidis, A, Vlachogianni, T, Fiotakis, K, Loridas, S. Pulmonary oxidative stress, inflammation and cancer: respirable particulate matter, fibrous dusts and ozone as major causes of lung carcinogenesis through reactive oxygen species mechanisms. Int J Environ Res Publ Health 2013;10:3886–907. https://doi.org/10.3390/ijerph10093886.Search in Google Scholar PubMed PubMed Central

38. Al-Ghafari, A, Elmorsy, E, Fikry, E, Alrowaili, M, Carter, WG. The heavy metals lead and cadmium are cytotoxic to human bone osteoblasts via induction of redox stress. PLoS One 2019;14:e0225341. https://doi.org/10.1371/journal.pone.0225341.Search in Google Scholar PubMed PubMed Central

39. Pasqua, LA, Damasceno, MV, Cruz, R, Matsuda, M, Martins, MAG, Marquezini, MV, et al.. Exercising in the urban center: inflammatory and cardiovascular effects of prolonged exercise under air pollution. Chemosphere 2020;254:126817. https://doi.org/10.1016/j.chemosphere.2020.126817.Search in Google Scholar PubMed

40. Fuhrmann, DC, Brüne, B. Mitochondrial composition and function under the control of hypoxia. Redox Biol 2017;12:208–15. https://doi.org/10.1016/j.redox.2017.02.012.Search in Google Scholar PubMed PubMed Central

41. Yan, C, Wang, Z, Liu, W, Pu, L, Li, R, Ai, C, et al.. Resveratrol ameliorates high altitude hypoxia-induced osteoporosis by suppressing the ROS/HIF signaling pathway. Molecules 2022;27:5538. https://doi.org/10.3390/molecules27175538.Search in Google Scholar PubMed PubMed Central

42. Shao, J, Liu, S, Zhang, M, Chen, S, Gan, S, Chen, C, et al.. A dual role of HIF1α in regulating osteogenesis-angiogenesis coupling. Stem Cell Res Ther 2022;13:59. https://doi.org/10.1186/s13287-022-02742-1.Search in Google Scholar PubMed PubMed Central

43. Lean, JM, Davies, JT, Fuller, K, Jagger, CJ, Kirstein, B, Partington, GA, et al.. A crucial role for thiol antioxidants in estrogen-deficiency bone loss. J Clin Invest 2003;112:915–23. https://doi.org/10.1172/jci200318859.Search in Google Scholar

44. Li, X, Lin, H, Zhang, X, Jaspers, RT, Yu, Q, Ji, Y, et al.. Notoginsenoside R1 attenuates oxidative stress-induced osteoblast dysfunction through JNK signalling pathway. 2021;25:11278–89, https://doi.org/10.1111/jcmm.17054.Search in Google Scholar PubMed PubMed Central

45. Mao, YX, Cai, WJ, Sun, XY, Dai, PP, Li, XM, Wang, Q, et al.. RAGE-dependent mitochondria pathway: a novel target of silibinin against apoptosis of osteoblastic cells induced by advanced glycation end products. Cell Death Dis 2018;9:674. https://doi.org/10.1038/s41419-018-0718-3.Search in Google Scholar PubMed PubMed Central

46. Deng, S, Dai, G, Chen, S, Nie, Z, Zhou, J, Fang, H, et al.. Dexamethasone induces osteoblast apoptosis through ROS-PI3K/AKT/GSK3β signaling pathway. Biomed Pharmacother 2019;110:602–8. https://doi.org/10.1016/j.biopha.2018.11.103.Search in Google Scholar PubMed

47. Li, Y, Wang, X. Chrysin attenuates high glucose-induced BMSC dysfunction via the activation of the PI3K/AKT/Nrf2 signaling pathway. Drug Des Dev Ther 2022;16:165–82. https://doi.org/10.2147/dddt.s335024.Search in Google Scholar

48. Li, Y, He, Y, Chen, G, Huang, Z, Yi, C, Zhang, X, et al.. Selenomethionine protects oxidative-stress-damaged bone-marrow-derived mesenchymal stem cells via an antioxidant effect and the PTEN/PI3K/AKT pathway. Exp Cell Res 2021;408:112864. https://doi.org/10.1016/j.yexcr.2021.112864.Search in Google Scholar PubMed

49. Li, K, Shen, Q, Xie, Y, You, M, Huang, L, Zheng, X. Incorporation of cerium oxide into hydroxyapatite coating protects bone marrow stromal cells against H(2)O(2)-induced inhibition of osteogenic differentiation. Biol Trace Elem Res 2018;182:91–104. https://doi.org/10.1007/s12011-017-1066-3.Search in Google Scholar PubMed

50. Hong, G, Chen, Z, Han, X, Zhou, L, Pang, F, Wu, R, et al.. A novel RANKL-targeted flavonoid glycoside prevents osteoporosis through inhibiting NFATc1 and reactive oxygen species. Clin Transl Med 2021;11:e392. https://doi.org/10.1002/ctm2.392.Search in Google Scholar PubMed PubMed Central

51. Chen, K, Qiu, P, Yuan, Y, Zheng, L, He, J, Wang, C, et al.. Pseurotin A inhibits osteoclastogenesis and prevents ovariectomized-induced bone loss by suppressing reactive oxygen species. Theranostics 2019;9:1634–50. https://doi.org/10.7150/thno.30206.Search in Google Scholar PubMed PubMed Central

52. Pan, W, Zheng, L, Gao, J, Ye, L, Chen, Z, Liu, S, et al.. SIS3 suppresses osteoclastogenesis and ameliorates bone loss in ovariectomized mice by modulating Nox4-dependent reactive oxygen species. Biochem Pharmacol 2022;195:114846. https://doi.org/10.1016/j.bcp.2021.114846.Search in Google Scholar PubMed

53. Bhagavatham, SKS, Kannan, V, Darshan, VMD, Sivaramakrishnan, V. Nucleotides modulate synoviocyte proliferation and osteoclast differentiation in macrophages with potential implications for rheumatoid arthritis. Biotech 2021;11:504. https://doi.org/10.1007/s13205-021-03052-8.Search in Google Scholar PubMed PubMed Central

54. Amrein, K, Scherkl, M, Hoffmann, M, Neuwersch-Sommeregger, S, Köstenberger, M, Tmava Berisha, A, et al.. Vitamin D deficiency 2.0: an update on the current status worldwide. Eur J Clin Nutr 2020;74:1498–513. https://doi.org/10.1038/s41430-020-0558-y.Search in Google Scholar PubMed PubMed Central

55. Wu, CY, Yang, HY, Luo, SF, Huang, JL, Lai, JH. Vitamin D supplementation in patients with juvenile idiopathic arthritis. Nutrients 2022;14:1538. https://doi.org/10.3390/nu14081538.Search in Google Scholar PubMed PubMed Central

56. Goltzman, D, Hendy, GN. The calcium-sensing receptor in bone--mechanistic and therapeutic insights. Nat Rev Endocrinol 2015;11:298–307. https://doi.org/10.1038/nrendo.2015.30.Search in Google Scholar PubMed

57. Hoseinzadeh, E, Taha, P, Wei, C, Godini, H, Ashraf, GM, Taghavi, M, et al.. The impact of air pollutants, UV exposure and geographic location on vitamin D deficiency. Food Chem Toxicol 2018;113:241–54. https://doi.org/10.1016/j.fct.2018.01.052.Search in Google Scholar PubMed

58. Mousavi, SE, Amini, H, Heydarpour, P, Amini Chermahini, F, Godderis, L. Air pollution, environmental chemicals, and smoking may trigger vitamin D deficiency: evidence and potential mechanisms. Environ Int 2019;122:67–90. https://doi.org/10.1016/j.envint.2018.11.052.Search in Google Scholar PubMed

59. Yang, C, Li, D, Tian, Y, Wang, P. Ambient air pollutions are associated with vitamin D status. Int J Environ Res Publ Health 2021;18:6887. https://doi.org/10.3390/ijerph18136887.Search in Google Scholar PubMed PubMed Central

60. He, H, Zeng, Y, Wang, X, Yang, L, Zhang, M, An, Z. Meteorological condition and air pollution exposure associated with vitamin D deficiency: a cross-sectional population-based study in China. Risk Manag Healthc Policy 2020;13:2317–24. https://doi.org/10.2147/rmhp.s273145.Search in Google Scholar PubMed PubMed Central

61. Feizabad, E, Hossein-Nezhad, A, Maghbooli, Z, Ramezani, M, Hashemian, R, Moattari, S. Impact of air pollution on vitamin D deficiency and bone health in adolescents. Arch Osteoporosis 2017;12:34. https://doi.org/10.1007/s11657-017-0323-6.Search in Google Scholar PubMed

62. Escobar, LM, Bendahan, Z, Bayona, A, Castellanos, JE, González, MC. Effect of vitamins D and E on the proliferation, viability, and differentiation of human dental pulp stem cells: an in vitro study. Int J Dent 2020;2020:8860840. https://doi.org/10.1155/2020/8860840.Search in Google Scholar PubMed PubMed Central

63. Al Saedi, A, Myers, DE, Stupka, N, Duque, G. 1,25(OH)(2)D(3) ameliorates palmitate-induced lipotoxicity in human primary osteoblasts leading to improved viability and function. Bone 2020;141:115672. https://doi.org/10.1016/j.bone.2020.115672.Search in Google Scholar PubMed

64. Kikuta, J, Kawamura, S, Okiji, F, Shirazaki, M, Sakai, S, Saito, H, et al.. Sphingosine-1-phosphate-mediated osteoclast precursor monocyte migration is a critical point of control in antibone-resorptive action of active vitamin D. Proc Natl Acad Sci USA 2013. 110; 7009–13. https://doi.org/10.1073/pnas.1218799110.Search in Google Scholar PubMed PubMed Central

65. Takasu, H, Sugita, A, Uchiyama, Y, Katagiri, N, Okazaki, M, Ogata, E, et al.. c-Fos protein as a target of anti-osteoclastogenic action of vitamin D, and synthesis of new analogs. J Clin Invest 2006;116:528–35. https://doi.org/10.1172/jci24742.Search in Google Scholar

66. Zhou, Q, Chen, J, Zhang, J, Zhou, F, Zhao, J, Wei, X, et al.. Toxicity and endocrine-disrupting potential of PM(2.5): association with particulate polycyclic aromatic hydrocarbons, phthalate esters, and heavy metals. Environ Pollut 2022;292:118349. https://doi.org/10.1016/j.envpol.2021.118349.Search in Google Scholar PubMed

67. Zhang, Y, Dong, S, Wang, H, Tao, S, Kiyama, R. Biological impact of environmental polycyclic aromatic hydrocarbons (ePAHs) as endocrine disruptors. Environ Pollut 2016;213:809–24. https://doi.org/10.1016/j.envpol.2016.03.050.Search in Google Scholar PubMed

68. Kim, I, Lee, K, Lee, S, Kim, SD. Characteristics and health effects of PM(2.5) emissions from various sources in Gwangju, South Korea. Sci Total Environ 2019;696:133890. https://doi.org/10.1016/j.scitotenv.2019.133890.Search in Google Scholar PubMed

69. Sun, H, Chen, H, Yao, L, Chen, J, Zhu, Z, Wei, Y, et al.. Sources and health risks of PM(2.5)-bound polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in a North China rural area. J Environ Sci 2020;95:240–7. https://doi.org/10.1016/j.jes.2020.03.051.Search in Google Scholar PubMed

70. Chen, YY, Kao, TW, Wang, CC, Wu, CJ, Zhou, YC, Chen, WL. Association between polycyclic aromatic hydrocarbons exposure and bone turnover in adults. Eur J Endocrinol 2020;182:333–41. https://doi.org/10.1530/eje-19-0750.Search in Google Scholar

71. Guo, J, Huang, Y, Bian, S, Zhao, C, Jin, Y, Yu, D, et al.. Associations of urinary polycyclic aromatic hydrocarbons with bone mass density and osteoporosis in U.S. adults, NHANES 2005-2010. Environ Pollut 2018;240:209–18. https://doi.org/10.1016/j.envpol.2018.04.108.Search in Google Scholar PubMed

72. Heo, JS, Lim, JY, Pyo, S, Yoon, DW. Lee, D, Ren, WX, et al.. Environmental benzopyrene attenuates stemness of placenta-derived mesenchymal stem cells via aryl hydrocarbon receptor. 2019;2019:7414015. https://doi.org/10.1155/2019/7414015.Search in Google Scholar PubMed PubMed Central

73. Elfawy, HA, Anupriya, S, Mohanty, S, Patel, P, Ghosal, S, Panda, PK, et al.. Molecular toxicity of Benzo(a)pyrene mediated by elicited oxidative stress infer skeletal deformities and apoptosis in embryonic zebrafish. Sci Total Environ 2021;789:147989. https://doi.org/10.1016/j.scitotenv.2021.147989.Search in Google Scholar PubMed

74. Zanaty, MI, Sawada, N, Kitani, Y, Nassar, HF, Mahmoud, HM, Hayakawa, K, et al.. Influence of benz[a]anthracene on bone metabolism and on liver metabolism in nibbler fish. Girella punctata 2020;17:1391. https://doi.org/10.3390/ijerph17041391.Search in Google Scholar PubMed PubMed Central

75. Izawa, T, Arakaki, R, Mori, H, Tsunematsu, T, Kudo, Y, Tanaka, E, et al.. The nuclear receptor AhR controls bone homeostasis by regulating osteoclast differentiation via the RANK/c-Fos signaling Axis. 2016;197:4639–50, https://doi.org/10.4049/jimmunol.1600822.Search in Google Scholar PubMed PubMed Central

76. Lee, LL, Lee, JS, Waldman, SD, Casper, RF, Grynpas, MD. Polycyclic aromatic hydrocarbons present in cigarette smoke cause bone loss in an ovariectomized rat model. Bone 2002;30:917–23. https://doi.org/10.1016/s8756-3282(02)00726-3.Search in Google Scholar PubMed

77. Cheng, CH, Chen, LR, Chen, KH. Osteoporosis due to hormone imbalance: an overview of the effects of estrogen deficiency and glucocorticoid overuse on. Bone Turnover 2022;23:1376. https://doi.org/10.3390/ijms23031376.Search in Google Scholar PubMed PubMed Central

78. Han, Y, Liu, W, Lei, R, Wang, M, Xue, Y. Exposure levels of PCDD/Fs and PCBs in human blood and the transplacental transfer characteristics in cord blood of newborns near the industrialized area. Chemosphere 2022;303:134995. https://doi.org/10.1016/j.chemosphere.2022.134995.Search in Google Scholar PubMed

79. Xue, Y, Xiao, Y, Liu, J, Karaplis, AC, Pollak, MR, Brown, EM, et al.. The calcium-sensing receptor complements parathyroid hormone-induced bone turnover in discrete skeletal compartments in mice. Am J Physiol Endocrinol Metabol 2012;302:E841–51. https://doi.org/10.1152/ajpendo.00599.2011.Search in Google Scholar PubMed PubMed Central

80. Herlin, M, Sánchez-Pérez, I, Esteban, J, Korkalainen, M, Barber, X, Finnilä, MAJ, et al.. Bone toxicity induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and the retinoid system: a causality analysis anchored in osteoblast gene expression and mouse data. Reprod Toxicol 2021;105:25–43. https://doi.org/10.1016/j.reprotox.2021.07.013.Search in Google Scholar PubMed

81. Choi, EM, Suh, KS, Jung, WW, Yun, S, Park, SY, Chin, SO, et al.. Catalpol protects against 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced cytotoxicity in osteoblastic MC3T3-E1 cells. J Appl Toxicol 2019;39:1710–9. https://doi.org/10.1002/jat.3896.Search in Google Scholar PubMed

82. Watson, ATD, Nordberg, RC, Loboa, EG, Kullman, SW. Evidence for aryl hydrocarbon receptor-mediated inhibition of osteoblast differentiation in human mesenchymal stem cells. Toxicol Sci 2019;167:145–56. https://doi.org/10.1093/toxsci/kfy225.Search in Google Scholar PubMed PubMed Central

83. Yu, TY, Kondo, T, Matsumoto, T, Fujii-Kuriyama, Y, Imai, Y. Aryl hydrocarbon receptor catabolic activity in bone metabolism is osteoclast dependent in vivo. Biochem Biophys Res Commun 2014;450:416–22. https://doi.org/10.1016/j.bbrc.2014.05.114.Search in Google Scholar PubMed

Received: 2023-02-19
Accepted: 2023-06-28
Published Online: 2023-08-03
Published in Print: 2024-12-17

© 2023 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Reviews
  3. A systematic review on the association between exposure to air particulate matter during pregnancy and the development of hypertensive disorders of pregnancy and gestational diabetes mellitus
  4. Screen time and childhood attention deficit hyperactivity disorder: a meta-analysis
  5. The association between polycystic ovary syndrome and environmental pollutants based on animal and human study; a systematic review
  6. Residues of carcinogenic pesticides in food: a systematic review
  7. The concentration of Lithium in water resources: A systematic review, meta-analysis and health risk assessment
  8. Polychlorinated biphenyls and thyroid function: a scoping review
  9. The European Union assessments of radiofrequency radiation health risks – another hard nut to crack (Review)
  10. Research progresses on the effects of heavy metals on the circadian clock system
  11. Diagnosing and managing heat exhaustion: insights from a systematic review of cases in the desert climate of Mecca
  12. Para-occupational exposure to chemical substances: a systematic review
  13. Association of the ACE2-Angiotensin1-7–Mas axis with lung damage caused by cigarette smoke exposure: a systematic review
  14. Impacts and mechanisms of PM2.5 on bone
  15. Impacts and potential mechanisms of fine particulate matter (PM2.5) on male testosterone biosynthesis disruption
  16. Exposure to perfluoroalkyl and polyfluoroalkyl substances and risk of stroke in adults: a meta-analysis
  17. Prevalence and concentration of aflatoxin M1 and ochratoxin A in cheese: a global systematic review and meta-analysis and probabilistic risk assessment
  18. The effect of polycyclic aromatic hydrocarbon biomarkers on cardiovascular diseases
  19. Biological effects of electromagnetic fields on insects: a systematic review and meta-analysis
  20. Letter to the Editor
  21. Monkeypox and drug repurposing: seven potential antivirals to combat the viral disease
Downloaded on 6.12.2025 from https://www.degruyterbrill.com/document/doi/10.1515/reveh-2023-0024/html?lang=en
Scroll to top button