최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기International journal of molecular sciences, v.22 no.9, 2021년, pp.4312 -
Li, Santie (College of Pharmacy and Research Institute of Pharmaceutical Sciences, Chonnam National University, Gwangju 61186, Korea) , Kim, Myeong-Ji (lisantie333@163.com (S.L.)) , Lee, Sung-Ho (audwlekt@naver.com (M.-J.K.)) , Jin, Litai (puzim23@gmail.com (S.-H.L.)) , Cong, Weitao (College of Pharmacy and Research Institute of Pharmaceutical Sciences, Chonnam National University, Gwangju 61186, Korea) , Jeong, Hye-Gwang (lisantie333@163.com (S.L.)) , Lee, Kwang-Youl (audwlekt@naver.com (M.-J.K.))
Metallothioneins (MTs) are intracellular cysteine-rich proteins, and their expressions are enhanced under stress conditions. MTs are recognized as having the ability to regulate redox balance in living organisms; however, their role in regulating osteoblast differentiation is still unclear. In this ...
1. Huang W. Yang S. Shao J. Li Y.P. Signaling and transcriptional regulation in osteoblast commitment and differentiation Front. Biosci. 2007 12 3068 3092 10.2741/2296 17485283
2. Tsukamoto M. Mori T. Wang K.Y. Okada Y. Fukuda H. Naito K. Yamanaka Y. Sabanai K. Nakamura E. Yatera K. Systemic bone loss, impaired osteogenic activity and type I muscle fiber atrophy in mice with elastase-induced pulmonary emphysema: Establishment of a COPD-related osteoporosis mouse model Bone 2019 120 114 124 10.1016/j.bone.2018.10.017 30342225
3. Manikandan M. Abuelreich S. Elsafadi M. Alsalman H. Almalak H. Siyal A. Hashmi J.A. Aldahmash A. Kassem M. Alfayez M. NR2F1 mediated down-regulation of osteoblast differentiation was rescued by bone morphogenetic protein-2 (BMP-2) in human MSC Differentiation 2018 104 36 41 10.1016/j.diff.2018.10.003 30445268
4. Soundharrajan I. Kim D.H. Srisesharam S. Kuppusamy P. Sivanesan R. Choi K.C. Limonene promotes osteoblast differentiation and 2-deoxy-d-glucose uptake through p38MAPK and Akt signaling pathways in C2C12 skeletal muscle cells Phytomedicine 2018 45 41 48 10.1016/j.phymed.2018.03.019 29573911
5. Lin G.L. Hankenson K.D. Integration of BMP, Wnt, and notch signaling pathways in osteoblast differentiation J. Cell. Biochem. 2011 112 3491 3501 10.1002/jcb.23287 21793042
6. Curtis E.M. Moon R.J. Dennison E.M. Harvey N.C. Cooper C. Recent advances in the pathogenesis and treatment of osteoporosis Clin. Med. 2016 16 360 364 10.7861/clinmedicine.16-4-360
7. Lynes M.A. Hidalgo J. Manso Y. Devisscher L. Laukens D. Lawrence D.A. Metallothionein and stress combine to affect multiple organ systems Cell. Stress. Chaperones. 2014 19 605 611 10.1007/s12192-014-0501-z 24584987
8. Bhandari S. Melchiorre C. Dostie K. Laukens D. Devisscher L. Louwrier A. Thees A. Lynes M.A. Detection and Manipulation of the Stress Response Protein Metallothionein Curr. Protoc. Toxicol. 2017 71 17.19.1 17.19.28 10.1002/cptx.17
9. Liu A.L. Zhang Z.M. Zhu B.F. Liao Z.H. Liu Z. Metallothionein protects bone marrow stromal cells against hydrogen peroxide-induced inhibition of osteoblastic differentiation Cell. Biol. Int. 2004 28 905 911 10.1016/j.cellbi.2004.09.004 15566960
10. Fong L. Tan K. Tran C. Cool J. Scherer M.A. Elovaris R. Coyle P. Foster B.K. Rofe A.M. Xian C.J. Interaction of dietary zinc and intracellular binding protein metallothionein in postnatal bone growth Bone 2009 44 1151 1162 10.1016/j.bone.2009.02.011 19254786
11. Crespi R. Capparé P. Romanos G.E. Mariani E. Benasciutti E. Gherlone E. Corticocancellous porcine bone in the healing of human extraction sockets: Combining histomorphometry with osteoblast gene expression profiles in vivo Int. J. Oral. Maxillofac. Implants. 2011 26 866 872 21841997
12. Zizzari V.L. Zara S. Tetè G. Vinci R. Gherlone E. Cataldi A. Biologic and clinical aspects of integration of different bone substitutes in oral surgery: A literature review Oral. Surg. Oral. Med. Oral. Pathol. Oral. Radiol. 2016 122 392 402 10.1016/j.oooo.2016.04.010 27496576
13. Crespi R. Capparè P. Gherlone E. Comparison of magnesium-enriched hydroxyapatite and porcine bone in human extraction socket healing: A histologic and histomorphometric evaluation Int. J. Oral. Maxillofac. Implants. 2011 26 1057 1062 22010090
14. Abedi-Amin A. Luzi A. Giovarruscio M. Paolone G. Darvizeh A. Agulló V.V. Sauro S. Innovative root-end filling materials based on calcium-silicates and calcium-phosphates J. Mater. Sci. Mater. Med. 2017 28 31 10.1007/s10856-017-5847-1 28108959
15. Bruschi G.B. Crespi R. Capparè P. Bravi F. Bruschi E. Gherlone E. Localized management of sinus floor technique for implant placement in fresh molar sockets Clin. Implant. Dent. Relat. Res. 2013 15 243 250 10.1111/j.1708-8208.2011.00348.x 21599829
16. Crespi R. Capparè P. Gherlone E. Sinus floor elevation by osteotome: Hand mallet versus electric mallet. A prospective clinical study Int. J. Oral. Maxillofac. Implants. 2012 27 1144 1150 23057028
17. Bruschi G.B. Crespi R. Capparè P. Gherlone E. Transcrestal sinus floor elevation: A retrospective study of 46 patients up to 16 years Clin. Implant. Dent. Relat. Res. 2012 14 759 767 10.1111/j.1708-8208.2010.00313.x 20977614
19. Otto F. Thornell A.P. Crompton T. Denzel A. Gilmour K.C. Rosewell I.R. Stamp G.W. Beddington R.S. Mundlos S. Olsen B.R. Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development Cell 1997 89 765 771 10.1016/S0092-8674(00)80259-7 9182764
20. Nakashima K. Zhou X. Kunkel G. Zhang Z. Deng J.M. Behringer R.R. de Crombrugghe B. The novel zinc finger-containing transcription factor osterix is required for osteoblast differentiation and bone formation Cell 2002 108 17 29 10.1016/S0092-8674(01)00622-5 11792318
21. Ryoo H.M. Hoffmann H.M. Beumer T. Frenkel B. Towler D.A. Stein G.S. Stein J.L. van Wijnen A.J. Lian J.B. Stage-specific expression of Dlx-5 during osteoblast differentiation: Involvement in regulation of osteocalcin gene expression Mol. Endocrinol. 1997 11 1681 1694 10.1210/mend.11.11.0011 9328350
22. Chiu R. Smith K.E. Ma G.K. Ma T. Smith R.L. Goodman S.B. Polymethylmethacrylate particles impair osteoprogenitor viability and expression of osteogenic transcription factors Runx2, osterix, and Dlx5 J. Orthop. Res. 2010 28 571 577 10.1002/jor.21035 20014320
23. Halliwell B. Free radicals, antioxidants, and human disease: Curiosity, cause, or consequence? Lancet 1994 344 721 724 10.1016/S0140-6736(94)92211-X 7915779
24. Harrison C. Bone disorders: Targeting NOX4 knocks down osteoporosis Nat. Rev. Drug. Discov. 2013 12 904 10.1038/nrd4182
25. Mody N. Parhami F. Sarafian T.A. Demer L.L. Oxidative stress modulates osteoblastic differentiation of vascular and bone cells Free. Radic. Biol. Med. 2001 31 509 519 10.1016/S0891-5849(01)00610-4 11498284
26. Arai M. Shibata Y. Pugdee K. Abiko Y. Ogata Y. Effects of reactive oxygen species (ROS) on antioxidant system and osteoblastic differentiation in MC3T3-E1 cells IUBMB. Life. 2007 59 27 33 10.1080/15216540601156188 17365177
27. Gao J. Feng Z. Wang X. Zeng M. Liu J. Han S. Xu J. Chen L. Cao K. Long J. SIRT3/SOD2 maintains osteoblast differentiation and bone formation by regulating mitochondrial stress Cell Death. Differ. 2018 25 229 240 10.1038/cdd.2017.144 28914882
28. Ruttkay-Nedecky B. Nejdl L. Gumulec J. Zitka O. Masarik M. Eckschlager T. Stiborova M. Adam V. Kizek R. The role of metallothionein in oxidative stress Int. J. Mol. Sci. 2013 14 6044 6066 10.3390/ijms14036044 23502468
29. Meloni G. Zovo K. Kazantseva J. Palumaa P. Vasák M. Organization and assembly of metal-thiolate clusters in epithelium-specific metallothionein-4 J. Biol. Chem. 2006 281 14588 14595 10.1074/jbc.M601724200 16556599
30. Ulsamer A. Ortuño M.J. Ruiz S. Susperregui A.R. Osses N. Rosa J.L. Ventura F. BMP-2 induces Osterix expression through up-regulation of Dlx5 and its phosphorylation by p38 J. Biol. Chem. 2008 283 3816 3826 10.1074/jbc.M704724200 18056716
31. Jang W.G. Kim E.J. Lee K.N. Son H.J. Koh J.T. AMP-activated protein kinase (AMPK) positively regulates osteoblast differentiation via induction of Dlx5-dependent Runx2 expression in MC3T3E1 cells Biochem. Biophys. Res. Commun. 2011 404 1004 1009 10.1016/j.bbrc.2010.12.099 21187071
32. Vašák M. Meloni G. Mammalian Metallothionein-3: New Functional and Structural Insights Int. J. Mol. Sci. 2017 18 1117 10.3390/ijms18061117
33. Cho Y.H. Lee S.H. Lee S.J. Kim H.N. Koh J.Y. A role of metallothionein-3 in radiation-induced autophagy in glioma cells Sci. Rep. 2020 10 2015 10.1038/s41598-020-58237-7 32029749
34. Oz G. Zangger K. Armitage I.M. Three-dimensional structure and dynamics of a brain specific growth inhibitory factor: Metallothionein-3 Biochemistry 2001 40 11433 11441 10.1021/bi010827l 11560491
35. Koh J.Y. Lee S.J. Metallothionein-3 as a multifunctional player in the control of cellular processes and diseases Mol. Brain. 2020 13 116 10.1186/s13041-020-00654-w 32843100
36. Park K.H. Choi Y. Yoon D.S. Lee K.M. Kim D. Lee J.W. Zinc Promotes Osteoblast Differentiation in Human Mesenchymal Stem Cells Via Activation of the cAMP-PKA-CREB Signaling Pathway. Stem Cells Dev. 2018 27 1125 1135 10.1089/scd.2018.0023 29848179
37. Tao H. Ge G. Liang X. Zhang W. Sun H. Li M. Geng D. ROS signaling cascades: Dual regulations for osteoclast and osteoblast Acta. Biochim. Biophys. Sin. 2020 52 1055 1062 10.1093/abbs/gmaa098 33085739
38. Schröder K. NADPH oxidases in bone homeostasis and osteoporosis Free. Radic. Biol. Med. 2019 132 67 72 10.1016/j.freeradbiomed.2018.08.036 30189265
39. Mandal C.C. Ganapathy S. Gorin Y. Mahadev K. Block K. Abboud H.E. Harris S.E. Ghosh-Choudhury G. Ghosh-Choudhury N. Reactive oxygen species derived from Nox4 mediate BMP2 gene transcription and osteoblast differentiation Biochem. J. 2011 433 393 402 10.1042/BJ20100357 21029048
40. Franceschi R.T. Ge C. Control of the Osteoblast Lineage by Mitogen-Activated Protein Kinase Signaling Curr. Mol. Biol. Rep. 2017 3 122 132 10.1007/s40610-017-0059-5 29057206
41. Liu Y. Ma X. Guo J. Lin Z. Zhou M. Bi W. Liu J. Wang J. Lu H. Wu G. All-trans retinoic acid can antagonize osteoblastogenesis induced by different BMPs irrespective of their dimerization types and dose-efficiencies Drug. Des. Devel. Ther. 2018 12 3419 3430 10.2147/DDDT.S178190
42. Franceschi R.T. Ge C. Xiao G. Roca H. Jiang D. Transcriptional regulation of osteoblasts Cells. Tissues. Organs. 2009 189 144 152 10.1159/000151747 18728356
43. Gómez-Moreno G. Guardia J. Ferrera M.J. Cutando A. Reiter R.J. Melatonin in diseases of the oral cavity Oral. Dis. 2010 16 242 247 10.1111/j.1601-0825.2009.01610.x 19682319
44. Stanford C.M. Surface modification of biomedical and dental implants and the processes of inflammation, wound healing and bone formation Int. J. Mol. Sci. 2010 11 354 369 10.3390/ijms11010354 20162020
45. Gherlone E.F. Capparé P. Tecco S. Polizzi E. Pantaleo G. Gastaldi G. Grusovin M.G. Implant Prosthetic Rehabilitation in Controlled HIV-Positive Patients: A Prospective Longitudinal Study with 1-Year Follow-Up Clin. Implant. Dent. Relat. Res. 2016 18 725 734 10.1111/cid.12353 25955953
46. Gherlone E.F. Capparé P. Tecco S. Polizzi E. Pantaleo G. Gastaldi G. Grusovin M.G. A Prospective Longitudinal Study on Implant Prosthetic Rehabilitation in Controlled HIV-Positive Patients with 1-Year Follow-Up: The Role of CD4+ Level, Smoking Habits, and Oral Hygiene Clin. Implant. Dent. Relat. Res. 2016 18 955 964 10.1111/cid.12370 26238779
47. Capparé P. Teté G. Romanos G.E. Nagni M. Sannino G. Gherlone E.F. The ‘All-on-four’ protocol in HIV-positive patients: A prospective, longitudinal 7-year clinical study Int. J. Oral. Implantol. 2019 12 501 510
48. Sberna M.T. Rizzo G. Zacchi E. Capparè P. Rubinacci A. A preliminary study of the use of peripheral quantitative computed tomography for investigating root canal anatomy Int. Endod. J. 2009 42 66 75 10.1111/j.1365-2591.2008.01452.x 18811596
49. Salgarelli A.C. Capparè P. Bellini P. Collini M. Usefulness of fine-needle aspiration in parotid diagnostics Oral. Maxillofac. Surg. 2009 13 185 190 10.1007/s10006-009-0182-4 19821124
50. Chapman G.A. Kay J. Kille P. Structural and functional analysis of the rat metallothionein III genomic locus Biochim. Biophys. Acta. 1999 1445 321 329 10.1016/S0167-4781(99)00053-6 10366715
51. Ogra Y. Suzuki K. Gong P. Otsuka F. Koizumi S. Negative regulatory role of Sp1 in metal responsive element-mediated transcriptional activation J. Biol. Chem. 2001 276 16534 16539 10.1074/jbc.M100570200 11279094
52. Niger C. Lima F. Yoo D.J. Gupta R.R. Buo A.M. Hebert C. Stains J.P. The transcriptional activity of osterix requires the recruitment of Sp1 to the osteocalcin proximal promoter Bone 2011 49 683 692 10.1016/j.bone.2011.07.027 21820092
53. Kang Y.J. The antioxidant function of metallothionein in the heart Proc. Soc. Exp. Biol. Med. 1999 222 263 273 10.1046/j.1525-1373.1999.d01-143.x 10601885
54. Fu Z. Guo J. Jing L. Li R. Zhang T. Peng S. Enhanced toxicity and ROS generation by doxorubicin in primary cultures of cardiomyocytes from neonatal metallothionein-I/II null mice Toxicol. Vitro. 2010 24 1584 1591 10.1016/j.tiv.2010.06.009
해당 논문의 주제분야에서 활용도가 높은 상위 5개 콘텐츠를 보여줍니다.
더보기 버튼을 클릭하시면 더 많은 관련자료를 살펴볼 수 있습니다.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.