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Current Molecular Pharmacology

Editor-in-Chief

ISSN (Print): 1874-4672
ISSN (Online): 1874-4702

Research Article

miR-18a-3p Encourages Apoptosis of Chondrocyte in Osteoarthritis via HOXA1 Pathway

Author(s): Baiyang Ding, Shujuan Xu, Xiumin Sun, Jianming Gao, Wenlei Nie and Hongguang Xu *

Volume 13, Issue 4, 2020

Page: [328 - 341] Pages: 14

DOI: 10.2174/1874467213666200204143740

Price: $65

Abstract

Background: Osteoarthritis is a disorder of joints featuring inflammation and degeneration of articular cartilage. Recently, miRs have been found to be associated in the regulation of chondrocytes and their apoptosis. miR-18a-3p has been found to be associated in the pathogenesis of rheumatoid arthritis, however, its role in articular cartilage tissues remains unclear.

Methods: C57BL/6 strain of mice and human cartilage tissue were used for the study. Histological analysis was done on isolated cartilage samples followed by TUNEL assay and immunohistochemical analysis. The chondrocytes were isolated from mouse and human cartilage tissues, RNA was isolated and subjected for qRT-PCR analysis. The chondrocytes were transfected with miR-18a-3p agomir, antagomir and siHOXA-1. Luciferase assay was done in 293T cells. Flow cytometry analysis was done and western blot analysis for studying the expression of proteins.

Results: The expression of miR-18a-3p was upregulated in chondrocytes after exposing them to interlukin- 1β (IL-1β) in vitro. The transfection of miR-18a-3p antagomir halted the IL-1β mediated apoptosis. The luciferase assay suggested that miR-18a-3p targets the 3’UTR region of HOXA1 gene thus blocking its expression. The treatment of HOXA1 siRNA demonstrated the rescuing effect of miR- 18a-3p antagomir on the apoptosis of chondrocytes. Treatment of miR-18a-3p antagomir attenuated the surface of cartilage in osteoarthritis mice and the agomir worsened it. TUNEL assay suggested decreased apoptosis and over-expression of HOAX1 in osteoarthritis mice post miR-18a-3p knockdown.

Conclusion: The findings confirmed the involvement of miR-18a-3p/HOXA1 pathway as a potential mechanism in the regulation of Osteoarthritis.

Keywords: Osteoarthritis, miR-18a-3p, HOXA-1, IL-1β, chondrocytes, chemical analysis.

Graphical Abstract

[1]
Siebelt, M.; Agricola, R.; Weinans, H.; Kim, Y.J. The role of imaging in early hip OA. Osteoarthritis Cartilage, 2014, 22(10), 1470-1480.
[http://dx.doi.org/10.1016/j.joca.2014.04.030 ] [PMID: 25278058]
[2]
Chapman, K.; Valdes, A.M. Genetic factors in OA pathogenesis. Bone, 2012, 51(2), 258-264.
[http://dx.doi.org/10.1016/j.bone.2011.11.026 ] [PMID: 22178404]
[3]
Rogers, E.L.; Reynard, L.N.; Loughlin, J. The role of inflammation-related genes in osteoarthritis. Osteoarthritis Cartilage, 2015, 23(11), 1933-1938.
[http://dx.doi.org/10.1016/j.joca.2015.01.003 ] [PMID: 26521739]
[4]
Yu, C.; Chen, W.P.; Wang, X.H. MicroRNA in osteoarthritis. J. Int. Med. Res., 2011, 39(1), 1-9.
[http://dx.doi.org/10.1177/147323001103900101 ] [PMID: 21672302]
[5]
Sondag, G.R.; Haqqi, T.M. The role of MicroRNAs and their targets in osteoarthritis. Curr. Rheumatol. Rep., 2016, 18(8), 56.
[http://dx.doi.org/10.1007/s11926-016-0604-x ] [PMID: 27402113]
[6]
Yan, S.; Wang, M.; Zhao, J.; Zhang, H.; Zhou, C.; Jin, L.; Zhang, Y.; Qiu, X.; Ma, B.; Fan, Q. MicroRNA-34a affects chondrocyte apoptosis and proliferation by targeting the SIRT1/p53 signaling pathway during the pathogenesis of osteoarthritis. Int. J. Mol. Med., 2016, 38(1), 201-209.
[http://dx.doi.org/10.3892/ijmm.2016.2618 ] [PMID: 27247228]
[7]
Li, Z.; Meng, D.; Li, G.; Xu, J.; Tian, K.; Li, Y. Overexpression of microRNA-210 promotes chondrocyte proliferation and extracellular matrix deposition by targeting HIF-3α in osteoarthritis. Mol. Med. Rep., 2016, 13(3), 2769-2776.
[http://dx.doi.org/10.3892/mmr.2016.4878 ] [PMID: 26861791]
[8]
Ambros, V. The functions of animal microRNAs. Nature, 2004, 431(7006), 350-355.
[http://dx.doi.org/10.1038/nature02871 ] [PMID: 15372042]
[9]
Miyaki, S.; Asahara, H. Macro view of microRNA function in osteoarthritis. Nat. Rev. Rheumatol., 2012, 8(9), 543-552.
[http://dx.doi.org/10.1038/nrrheum.2012.128 ] [PMID: 22890245]
[10]
Woods, S.; Barter, M.J.; Elliott, H.R.; McGillivray, C.M.; Birch, M.A.; Clark, I.M.; Young, D.A. miR-324-5p is up regulated in end-stage osteoarthritis and regulates Indian Hedgehog signalling by differing mechanisms in human and mouse. Matrix Biol., 2019, 77, 87-100.
[http://dx.doi.org/10.1016/j.matbio.2018.08.009 ] [PMID: 30193893]
[11]
Yuan, Y.; Zhang, G.Q.; Chai, W.; Ni, M.; Xu, C.; Chen, J.Y. Silencing of microRNA-138-5p promotes IL-1β-induced cartilage degradation in human chondrocytes by targeting FOXC1: miR-138 promotes cartilage degradation. Bone Joint Res., 2016, 5(10), 523-530.
[http://dx.doi.org/10.1302/2046-3758.510.BJR-2016-0074.R2 ] [PMID: 27799147]
[12]
Kuo, G.; Wu, C.Y.; Yang, H.Y. MiR-17-92 cluster and immunity. J. Formos. Med. Assoc., 2019, 118(1 Pt 1), 2-6.
[http://dx.doi.org/10.1016/j.jfma.2018.04.013 ] [PMID: 29857952]
[13]
Orlowsky, E.W.; Kraus, V.B. The role of innate immunity in osteoarthritis: when our first line of defense goes on the offensive. J. Rheumatol., 2015, 42(3), 363-371.
[http://dx.doi.org/10.3899/jrheum.140382 ] [PMID: 25593231]
[14]
Shen, K.; Cao, Z.; Zhu, R.; You, L.; Zhang, T. The dual functional role of MicroRNA-18a (miR-18a) in cancer development. Clin. Transl. Med., 2019, 8(1), 32.
[http://dx.doi.org/10.1186/s40169-019-0250-9 ] [PMID: 31873828]
[15]
Kamekura, S.; Hoshi, K.; Shimoaka, T.; Chung, U.; Chikuda, H.; Yamada, T.; Uchida, M.; Ogata, N.; Seichi, A.; Nakamura, K.; Kawaguchi, H. Osteoarthritis development in novel experimental mouse models induced by knee joint instability. Osteoarthritis Cartilage, 2005, 13(7), 632-641.
[http://dx.doi.org/10.1016/j.joca.2005.03.004 ] [PMID: 15896985]
[16]
Pritzker, K.P.; Gay, S.; Jimenez, S.A.; Ostergaard, K.; Pelletier, J.P.; Revell, P.A.; Salter, D.; van den Berg, W.B. Osteoarthritis cartilage histopathology: grading and staging. Osteoarthritis Cartilage, 2006, 14(1), 13-29.
[http://dx.doi.org/10.1016/j.joca.2005.07.014 ] [PMID: 16242352]
[17]
Gosset, M.; Berenbaum, F.; Thirion, S.; Jacques, C. Primary culture and phenotyping of murine chondrocytes. Nat. Protoc., 2008, 3(8), 1253-1260.
[http://dx.doi.org/10.1038/nprot.2008.95 ] [PMID: 18714293]
[18]
Hwang, H.S.; Kim, H.A. Chondrocyte apoptosis in the pathogenesis of osteoarthritis. Int. J. Mol. Sci., 2015, 16(11), 26035-26054.
[http://dx.doi.org/10.3390/ijms161125943 ] [PMID: 26528972]
[19]
Latourte, A.; Cherifi, C.; Maillet, J.; Ea, H.K.; Bouaziz, W.; Funck-Brentano, T.; Cohen-Solal, M.; Hay, E.; Richette, P. Systemic inhibition of IL-6/Stat3 signalling protects against experimental osteoarthritis. Ann. Rheum. Dis., 2017, 76(4), 748-755.
[http://dx.doi.org/10.1136/annrheumdis-2016-209757 ] [PMID: 27789465]
[20]
Taniguchi, Y.; Kawata, M.; Ho Chang, S.; Mori, D.; Okada, K.; Kobayashi, H.; Sugita, S.; Hosaka, Y.; Inui, H.; Taketomi, S.; Yano, F.; Ikeda, T.; Akiyama, H.; Mills, A.A.; Chung, U.I.; Tanaka, S.; Kawaguchi, H.; Saito, T. Regulation of chondrocyte survival in mouse articular cartilage by p63. Arthritis Rheumatol., 2017, 69(3), 598-609.
[http://dx.doi.org/10.1002/art.39976 ] [PMID: 27792866]
[21]
Zhang, C.; Lin, S.; Li, T.; Jiang, Y.; Huang, Z.; Wen, J.; Cheng, W.; Li, H. Mechanical force-mediated pathological cartilage thinning is regulated by necroptosis and apoptosis. Osteoarthritis Cartilage, 2017, 25(8), 1324-1334.
[http://dx.doi.org/10.1016/j.joca.2017.03.018 ] [PMID: 28396243]
[22]
Ouboussad, L.; Hunt, L.; Hensor, E.M.A.; Nam, J.L.; Barnes, N.A.; Emery, P.; McDermott, M.F.; Buch, M.H. Profiling microRNAs in individuals at risk of progression to rheumatoid arthritis. Arthritis Res. Ther., 2017, 19(1), 288.
[http://dx.doi.org/10.1186/s13075-017-1492-9 ] [PMID: 29273071]
[23]
Zhou, Z.; Du, D.; Chen, A.; Zhu, L. Circular RNA expression profile of articular chondrocytes in an IL-1β-induced mouse model of osteoarthritis. Gene, 2018, 644, 20-26.
[http://dx.doi.org/10.1016/j.gene.2017.12.020 ] [PMID: 29247798]
[24]
Yang, G.; Li, S.; Li, B.; Cheng, L.; Jiang, P.; Tian, Z.; Sun, S. Protective effects of garlic-derived S-allylmercaptocysteine on IL-1b-stimulated chondrocytes by regulation ofMMPs/TIMP-1 ratio and type II collagen expression via suppression of NF-kB pathway. Bio. Med. Res. Int., 2017., 20178686207
[http://dx.doi.org/10.1155/2017/8686207 ] [PMID: 29333456]
[25]
Komatsu, S.; Ichikawa, D.; Takeshita, H.; Morimura, R.; Hirajima, S.; Tsujiura, M.; Kawaguchi, T.; Miyamae, M.; Nagata, H.; Konishi, H.; Shiozaki, A.; Otsuji, E. Circulating miR-18a: a sensitive cancer screening biomarker in human cancer. In Vivo, 2014, 28(3), 293-297.
[PMID: 24815829]
[26]
Sarno, J.; Schatz, F.; Huang, S.J.; Lockwood, C.; Taylor, H.S. Thrombin and interleukin-1beta decrease HOX gene expression in human first trimester decidual cells: implications for pregnancy loss. Mol. Hum. Reprod., 2009, 15(7), 451-457.
[http://dx.doi.org/10.1093/molehr/gap030 ] [PMID: 19389728]
[27]
Chen, L.; Hu, N.; Wang, C.; Zhao, H.; Gu, Y. Long non-coding RNA CCAT1 promotes multiple myeloma progression by acting as a molecular sponge of miR-181a-5p to modulate HOXA1 expression. Cell Cycle, 2018, 17(3), 319-329.
[http://dx.doi.org/10.1080/15384101.2017.1407893 ] [PMID: 29228867]
[28]
Zhang, X.; Zhu, T.; Chen, Y.; Mertani, H.C.; Lee, K.O.; Lobie, P.E. Human growth hormone-regulated HOXA1 is a human mammary epithelial oncogene. J. Biol. Chem., 2003, 278(9), 7580-7590.
[http://dx.doi.org/10.1074/jbc.M212050200 ] [PMID: 12482855]
[29]
Xiao, F.; Bai, Y.; Chen, Z.; Li, Y.; Luo, L.; Huang, J.; Yang, J.; Liao, H.; Guo, L. Downregulation of HOXA1 gene affects small cell lung cancer cell survival and chemoresistance under the regulation of miR-100. Eur. J. Cancer, 2014, 50(8), 1541-1554.
[http://dx.doi.org/10.1016/j.ejca.2014.01.024 ] [PMID: 24559685]
[30]
Wang, H.; Zhang, H.; Sun, Q.; Wang, Y.; Yang, J.; Yang, J.; Zhang, T.; Luo, S.; Wang, L.; Jiang, Y.; Zeng, C.; Cai, D.; Bai, X. Intra-articular delivery of antago-miR-483-5p inhibits osteoarthritis by modulating matrilin 3 and tissue inhibitor of metalloproteinase 2. Mol. Ther., 2017, 25(3), 715-727.
[http://dx.doi.org/10.1016/j.ymthe.2016.12.020 ] [PMID: 28139355]
[31]
Hu, G.; Zhao, X.; Wang, C.; Geng, Y.; Zhao, J.; Xu, J.; Zuo, B.; Zhao, C.; Wang, C.; Zhang, X. MicroRNA-145 attenuates TNF-α-driven cartilage matrix degradation in osteoarthritis via direct suppression of MKK4. Cell Death Dis., 2017, 8(10), e3140.
[http://dx.doi.org/10.1038/cddis.2017.522 ] [PMID: 29072705]

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