JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES) ›› 2017, Vol. 55 ›› Issue (7): 31-37.doi: 10.6040/j.issn.1671-7554.0.2017.198

Previous Articles     Next Articles

Effects of carbon monoxide releasing molecule-3 on the osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells

LI Jingyuan1, SONG Ling2, LIN Song3, SONG Hui4   

  1. 1. Department of Oral Mucosal Diseases, Stomatological Hospital of Shandong University, Shandong Provincial Key Laboratory of Oral Tissue Regeneration, Jinan 250012, Shandong, China;
    2. Department of Stomatology, Qingdao Municipal Hospital, Qingdao 266011, Shandong, China;
    3. Department of Pediatric Dentistry, Jinan Stomatological Hospital, Jinan 250001, Shandong, China;
    4. Department of VIP Clinic, Stomatological Hospital of Shandong University, Shandong Provincial Key Laboratory ofOral Tissue Regeneration, Jinan 250012, Shandong, China
  • Received:2017-03-07 Online:2017-07-10 Published:2017-07-10

Abstract: Objective To investigate the effects of carbon monoxide releasing molecule-3(CORM-3)on the osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells(BMSCs). Methods The BMSCs were divided into 2 groups, group A and group B. Group A was subdivided into osteogenic group, 100 μmol/L CORM-3 group, 200 μmol/L CORM-3 group, 400 μmol/L CORM-3 group and control group. Group B was subdivided into osteogenic 山 东 大 学 学 报 (医 学 版)55卷7期 -李景媛,等.不同浓度一氧化碳释放分子-3对大鼠骨髓间充质干细胞成骨分化的影响 \=-group, 100 μmol/L CORM-3-osteogenic group, 200 μmol/L CORM-3-osteogenic group, 400 μmol/L CORM-3-osteogenic group and control group. The mRNA and protein expressions of Runx2 and OPN were detected with Real-time PCR and Western blotting. The cell mineralization was determined with alizarin red staining. Data obtained were analyzed with SPSS 19.0 software. Results CORM-3 at concentrations of 100 μmol/L and 200 μmol/L could significantly promote the proliferation of BMSCs(P=0.034, P<0.001). The mRNA expressions of Runx2 and OPN in 200 μmol/L and 400 μmol/L CORM-3-osteogenic groups were significantly higher than those in the osteogenic group on day 7(Runx2: P=0.005, P=0.006; OPN: P=0.010, P=0.028). Meanwhile, the protein expressions of Runx2 and OPN on day 7 and cell mineralization on day 21 in 200 μmol/L and 400 μmol/L CORM-3-osteogenic groups were enhanced compared with the osteogenic group, and the 200 μmol/L group had better results than the 400 μmol/L group. Conclusion CORM-3 may promote osteogenic differentiation of BMSCs and 200 μmol/L is the suitable concentration.

Key words: Carbon monoxide releasing molecules-3, Osteogenic differentiation, Bone marrow-derived mesenchymal stem cells, Runt-related transcription factor 2, Osteopontin

CLC Number: 

  • R781.4
[1] Loesche WJ, Grossman NS. Periodontal disease as a specific, albeit chronic, infection: diagnosis and treatment[J]. Clin Microbiol Rev, 2001, 14(4): 727-752.
[2] Rauh J, Milan F, Gunther KP, et al. Bioreactor systems for bone tissue engineering[J]. Tissue Eng Part B Rev, 2011, 17(4): 263-280.
[3] Tsai TL, Li WJ. Identification of bone marrow-derived soluble factors regulating human mesenchymal stem cells for bone regeneration[J]. Stem Cell Reports, 2017, 8(2):387-400.
[4] Motterlini R, Mann BE, Johnson TR, et al. Bioactivity and pharmacological actions of carbon monoxide-releasing molecules[J]. Curr Pharm Des, 2003, 9(30): 2525-2539.
[5] Luria EA, Owen ME, Friedenstein AJ, et al.Bone formation in organ cultures of bone marrow[J]. Cell Tissue Res, 1987, 248(2): 449-454.
[6] Corsetti A, Bahuschewskyj C, Ponzoni D, et al. Repair of bone defects using adipose-derived stem cells combined with alpha-tricalcium phosphate and gelatin sponge scaffolds in a rat model[J]. J Appl Oral Sci, 2017, 25(1): 10-19.
[7] Meng J, Ma X, Wang N, et al. Activation of GLP-1 receptor promotes bone marrow stromal cell osteogenic differentiation through β-Catenin [J]. Stem Cell Reports, 2016, 6(4): 579-591.
[8] Ma C, Wei Q, Cao B, et al. A multifunctional bioactive material that stimulates osteogenesis and promotes the vascularization bone marrow stem cells and their resistance to bacterial infection [J]. PLoS One, 2017, 12(3): e0172499. doi: 10.1371/journal.pone.0172499. eCollection 2017.
[9] Pittenger MF, Mackay AM, Beck SC, et al. Multilineage potential of adult human mesenchymal stem cells[J]. Science, 1999, 284(5411): 143-147.
[10] Lu T, Huang YX, Zhang C, et al. Effect of pulsed electromagnetic field therapy on the osteogenic and adipogenic differentiation of bone marrow mesenchymal stem cells[J]. Genet Mol Res, 2015, 14(3):11535-11542.
[11] Yin H, Wang Y, Sun Z, et al. Induction of mesenchymal stem cell chondrogenic differentiation and functional cartilage microtissue formation for in vivo cartilage regeneration by cartilage extracellular matrix-derived particles [J]. Acta Biomater, 2016, 33: 96-109. doi: 10.1016/j.actbio.2016.01.024. Epub 2016 Jan 21.
[12] Maiti SK, Ninu AR, Sangeetha P, et al. Mesenchymal stem cells-seeded bio-ceramic construct for bone regeneration in large critical-size bone defect in rabbit [J]. J Stem Cells Regen Med, 2016, 12(2): 87-99.
[13] Bornes TD, Jomha NM, Mulet-Sierra A, et al. Porous scaffold seeding and chondrogenic differentiation of BMSC-seeded scaffolds [J]. Bio Protoc, 2015, 5(24). pii: e1693.
[14] Vander Plas A, Ni Jweide PJ. Cell-cell interaction in the osteogenic compartment of bone[J]. Bone, 1988, 9(2):107-111.
[15] Vahabi S, Torshabi M, Mohammadi M. Osteoinductive activity of DFDBA materials versus growth factors on gene expression of MG-63 cells: an in vitro study [J]. J Long Term Eff Med Implants, 2016, 26(2):133-142.
[16] Fu R, Selph S, McDonagh M, et al. Effectiveness and harms of recombinant human bone morphogenetic protein-2 in spine fusion: a systematic review and meta-analysis [J]. Ann Intern Med, 2013, 158(12):890-902.
[17] Gothard D, Smith EL, Kanczler JM, et al. Tissue engineered bone using select growth factors: a comprehensive review of animal studies and clinical translation studies in man [J]. Eur Cells Mater, 2014, 28: 166-208. discussion 207-8.
[18] Mesfin A, Buchowski JM, Zebala LP, et al. High-dose rhBMP-2 for adults: major and minor complications: a study of 502 spine cases [J]. J Bone Joint Surg Am, 2013, 95(17): 1546-1553.
[19] Qureshi OS, Zeb A, Akram M, et al. Enhanced acute anti-inflammatory effects of CORM-2-loaded nanoparticles via sustained carbon monoxide delivery [J]. Eur J Pharm Biopharm, 2016, 108: 187-195. doi: 10.1016/j.ejpb.2016.09.008. Epub 2016 Sep 12.
[20] Jiang L, Fei D, Gong R, et al. CORM-2 inhibits TXNIP/NLRP3 inflammasome pathway in LPS-induced acute lung injury [J]. Inflamm Res, 2016, 65(11): 905-915.
[21] Fayad-Kobeissi S, Ratovonantenaina J, Dabiré H, et al. Vascular and angiogenic activities of CORM-401, an oxidant-sensitive CO-releasing molecule [J]. Biochem Pharmacol, 2016, 102: 64-77. doi: 10.1016/j.bcp.2015.12.014. Epub 2015 Dec 22.
[22] Song H, Hoeger S, Hillebrands JL, et al. CORMs protect endothelial cells during cold preservation, resulting in inhibition of intimal hyperplasia after aorta transplantation in rats [J]. Transpl Int, 2010, 23(11): 1144-1153.
[23] 魏玲玲, 侯萌, 王苹, 等. 一氧化碳释放分子对大鼠实验性牙周炎的影响[J].华西口腔医学杂志, 2014, 32(1): 23-26. WEI Lingling, HOU Meng, WANG Ping, et al. Effect of carbon monoxide releasing molecule on experimental periodontitis in rats [J]. West China Journal of Stomatology, 2014, 32(1): 23-26.
[24] Komori T, Yagi H, Nomura S, et al. Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts[J]. Cell, 1997, 89(5): 755-764.
[25] 赵华强, 侯萌, 魏玲玲, 等. 一氧化碳对炎症环境下人牙龈成纤维细胞黏附分子表达影响的机制研究[J]. 华西口腔医学杂志, 2013, 31(4): 420-424. ZHAO Huaqiang, HOU Meng, WEI Lingling, et al. Mechanism of carbon monoxide affecting the expression of cellular adhesion molecule under stimulation of inflammatory cytokines to human gingival fibroblasts [J]. West China Journal of Stomatology, 2013, 31(4): 420-424.
[1] LI Shanshan, YANG Jing, ZHANG Jin. Post-transcriptional regulation mechanism of sclerostin in mice [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(3): 43-48.
[2] DING Feng, DONG Yabing, ZHAO Huaqiang, ZHU Guoxiong, WU Gaoyi. Effect of osteopontin through NF-kappaB signaling pathway in the temporomandibular joint of rats subjected to chronic sleep deprivation [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2016, 54(9): 41-47.
[3] GAO Peng, SHEN Fangzhen, XIAO Wenjing, XIU Yuande, ZHOU Lingling. Correlation between the expressions of Runx2 and Ezrin and postoperative metastasis in patients with stage IB non-small cell lung cancer [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2015, 53(1): 63-66.
[4] YU Hua-long1, HU San-yuan2. Expression of osteopontin in the colorectal
adenoma-carcinoma sequence
[J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2012, 50(11): 84-87.
[5] XING Jie-long, XU Yu-bin, ZHANG Yan, XU Chang-xian, MENG Guo-wei, LI Yong, BAO Wei-guo. Transplantation of Y chromosome labeled bone marrow-derived mesenchymal  stem cells  into rat hearts with myocardial infarction [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(7): 74-.
[6] WANG Xing-miao1, LI Meng-quan1, WANG Li-juan2, SU Jing1, HU Di1. Expressions of Caspase-3, OPN and Ezrin in invasive ductal  carcinoma of breasts and their clinical significance [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(4): 141-145.
[7] HA Chun-fang1,2, XIAO Cheng-ming1, ZHANG Sheng-ning1, LIU Pei-shu2 . Establishment and evaluation of an opening-method model of  endometriosis  in rats [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(1): 62-66.
[8] LI Deqiang1, LIU Peilai1, TANG Tingting2, LU Jianxi2, ZHANG Yuankai1, LI Deqiang1, LIU Peilai1, TANG Tingting2, LU Jianxi2, ZHANG Y. Effects of dynamic culture on the osteogenic differentiation of BMSCs in the 3D porous scaffold [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2010, 48(4): 49-53.
[9] XU Lin, ZHANG Weidong, WANG Zhaopeng, ZHANG Yueying, JIA Qing. Inhibitive effect of polypeptide extract from scorpion venom(PESV)  on the growth and metastasis of Lewis lung carcinomas [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2010, 48(1): 82-.
[10] . Effects of Niaoduqing on expressions of the fibrogenetic factors  in rats with Adriamycin nephropathy [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2009, 47(12): 38-41.
[11] LI Huihui1, ZHANG Linfan2, GU Shuang3, ZHANG Xiangning1
. Osteopontin promotes the invasiveness of human ovarian
carcinoma cell line SKOV3: an experimental study
[J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2009, 47(01): 38-41.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!