Establishment of immortalized rabbit bone marrow mesenchymal stem cells and a preliminary study of their osteogenic differentiation capability

Yao Zhang , Chang Xu , Yun Huang , Dongmei Tan , Wenping Luo , Yan Zhang , Yi Tan

Animal Models and Experimental Medicine ›› 2024, Vol. 7 ›› Issue (6) : 824 -834.

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Animal Models and Experimental Medicine ›› 2024, Vol. 7 ›› Issue (6) : 824 -834. DOI: 10.1002/ame2.12513
ORIGINAL ARTICLE

Establishment of immortalized rabbit bone marrow mesenchymal stem cells and a preliminary study of their osteogenic differentiation capability

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Abstract

Background: A stable and standardized source of mesenchymal stem cells is a prerequisite for bone repair tissue engineering research and application. We aimed to establish a stable cell line of bone marrow mesenchymal stem cells from New Zealand rabbits and explore their osteogenic differentiation capacity.

Methods: Primary rabbit bone marrow mesenchymal stem cells (RBMSCs) were isolated and immortalized via retroviral expression of SV40 Large T antigen (LTA). To assess the osteogenic differentiation capacity of the cells in vitro, we studied the alkaline phosphatase (ALP) expression level and calcium deposition in bone morphogenetic protein 9 (BMP9)-induced immortalized cells using ALP staining and quantification, as well as alizarin red staining. Ectopic bone formation by the cells was assessed using micro-computed tomography (µCT) and histological examination.

Results: The immortalized cell line we established using SV40 LTA, which we termed iRBMSCs, was non-tumorigenic and maintained long-term proliferative activity. We further discovered that BMP9 (MOI = 30) effectively induced the osteogenic differentiation capacity of iRBMSCs in vitro, and there was a synergy with GelMA hydrogel in inducing osteogenic differentiation of the iRBMSCs in vivo.

Conclusion: We confirmed that iRBMSCs are promising as a stable cell line source for bone defect repair engineering.

Keywords

bone marrow mesenchymal stem cells / bone morphogenetic protein 9 / GelMA hydrogel / immortalization

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Yao Zhang, Chang Xu, Yun Huang, Dongmei Tan, Wenping Luo, Yan Zhang, Yi Tan. Establishment of immortalized rabbit bone marrow mesenchymal stem cells and a preliminary study of their osteogenic differentiation capability. Animal Models and Experimental Medicine, 2024, 7(6): 824-834 DOI:10.1002/ame2.12513

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References

[1]

Phukan R, Herzog T, Boland PJ, et al. How does the level of sacral resection for primary malignant bone tumors affect physical and mental health, pain, mobility, incontinence, and sexual function? Clin Orthop Relat Res. 2016;474(3):687-696.

[2]

Majidinia M, Sadeghpour A, Yousefi B. The roles of signaling pathways in bone repair and regeneration. J Cell Physiol. 2018;233(4):2937-2948.

[3]

Giannoudis PV, Dinopoulos H, Tsiridis E. Bone substitutes: an update. Injury. 2005;36(36 Suppl 3):S20-S27.

[4]

Ruan W, Xue Y, Zong Y, Sun C. Effect of BMPs and Wnt3a co expression on the osteogenetic capacity of osteoblasts. Mol Med Rep. 2016;14(5):4328-4334.

[5]

Lan TX, Luo M, Wei XW. Mesenchymal stem/stromal cells in cancer therapy. J Hematol Oncol. 2021;14:195-211.

[6]

Bruder SP, Jaiswal N, Haynesworth SE. Growth kinetics, self-renewal, and the osteogenic potential of purified human mesenchymal stem cells during extensive subculltivation and following cryopreservation. J Cell Biochem. 1998;64:278-294.

[7]

Zuk PA, Zhu M, Ashjian P, et al. Human adipose tissue is a source of multipotent stem cells. Mol Biol Cell. 2002;13:4279-4295.

[8]

Covas DT, Siufi JL, Silva AR, et al. Isolation and culture of umbilical vein mesenchymal stem cells. Braz J Med Biol Res. 2003;36:1179-1183.

[9]

Rodriguez-Lozano FJ, Bueno C, Insausti CL, et al. Mesenchymal stem cells derived from dental tissues. Int Endod J. 2011;44:800-806.

[10]

Mohamed-Ahmed S, Yassin MA, Rashad A, et al. Comparison of bone regenerative capacity of donor-matched human adipose-derived and bone marrow mesenchymal stem cells. Cell Tissue Res. 2021;383(3):1061-1075.

[11]

Gorgun C, Palamà MEF, Reverberi D, et al. Role of extracellular vesicles from adipose tissue-and bone marrow-mesenchymal stromal cells in endothelial proliferation and chondrogenesis. Stem Cells Transl Med. 2021;10(12):1680-1695.

[12]

Ozden AO, Dikmen T, Nawaz S, et al. Comparison of proliferation and osteogenic differentiation potential of bovine adipose tissue and bone marrow derived stem cells. Biotech Histochem. 2023;98(4):267-279.

[13]

Jin YZ, Lee JH. Mesenchymal stem cell therapy for bone regeneration. Clin Orthop Surg. 2018;10(3):271-278.

[14]

Zhou T, Yuan Z, Weng J, et al. Challenges and advances in clinical applications of mesenchymal stromal cells. J Hematol Oncol. 2021;14:2-26.

[15]

Voloshin N, Tyurin-Kuzmin P, Karagyaur M, Akopyan Z, Kulebyakin K. Practical use of immortalized cells in medicine: current advances and future perspectives. Int J Mol Sci. 2023;24:12716-12738.

[16]

Lenz LS, Wink MR. The other side of the coin: mesenchymal stromal cell immortalization beyond evasion of senescence. Hum Cell. 2023;36(5):1593-1603.

[17]

Porrás A, Bennett J, Howe A, et al. A novel simian virus 40 early-region domain mediates transactivation of the cyclin a promoter by small-t antigen and is required for transformation in small-t antigen-dependent assays. J Virol. 1996;70:6902-6908.

[18]

Chen Y, Hu S, Wang M, et al. Characterization and establishment of an immortalized rabbit melanocyte cell line using the SV40 large T antigen. Int J Mol Sci. 2019;20(19):4874-4886.

[19]

Hogan BL. Bone morphogenetic proteins: multifunctional regulators of vertebrate development. Genes Dev. 1996;10(13):1580-1594.

[20]

Mostafa S, Pakvasa M, Coalson E, et al. The wonders of BMP9: from mesenchymal stem cell differentiation, angiogenesis, neurogenesis, tumorigenesis, and metabolism to regenerative medicine. Genes & Diseases. 2019;6(3):201-223.

[21]

Zaszczyńska A, Moczulska-Heljak M, Gradys A, Sajkiewicz P. Advances in 3D Printing for Tissue Engineering. Materials (Basel). 2021 Jun 8;14(12):3149.

[22]

Guo A, Zhang S, Yang R, Sui C. Enhancing the mechanical strength of 3D printed GelMA for soft tissue engineering applications. Materials Today Bio. 2023;24:100939-100954.

[23]

Zhang H, Wang J, Deng F, et al. Canonical Wnt signaling acts synergistically on BMP9-induced osteo/odontoblastic differentiation of stem cells of dental apical papilla (SCAPs). Biomaterials. 2015;39:145-154.

[24]

Chen Q, Zheng L, Zhang Y, et al. Special AT-rich sequence-binding protein 2 (Satb2) synergizes with Bmp9 and is essential for osteo/odontogenic differentiation of mouse incisor mesenchymal stem cells. Cell Prolif. 2021;54(4):e1301.

[25]

Perez JR, Kouroupis D, Li DJ, Best TM, Kaplan L, Correa D. Tissue engineering and cell-based therapies for fractures and bone defects. Front Bioeng Biotechnol. 2018;31(6):105-121.

[26]

Lynn JV, Ranganathan K, Luby AO, et al. Therapeutic efficacy of adipose-derived stem cells versus bone marrow stromal cells for irradiated mandibular fracture repair. Ann Plast Surg. 2022;89(4):459-646.

[27]

Kunimatsu R, Nakajima K, Awada T, et al. Comparative characterization of stem cells from human exfoliated deciduous teeth, dental pulp, and bone marrow-derived mesenchymal stem cells. Biochem Biophys Res Commun. 2018;501(1):193-198.

[28]

Tan SL, Ahmad TS, Selvaratnam L, Kamarul T. Isolation, characterization and the multi-lineage differentiation potential of rabbit bone marrow-derived mesenchymal stem cells. J Anat. 2013;222(4):437-450.

[29]

Jha KK, Banga S, Palejwala V, Ozer HL. SV40-mediated immortalization. Exp Cell Res. 1998;245(1):1-7.

[30]

Hu X, Li L, Yu X, et al. CRISPR/Cas9-mediated reversibly immortalized mouse bone marrow stromal stem cells (BMSCs) retain multipotent features of mesenchymal stem cells (MSCs). Oncotarget. 2017;8:111847-111865.

[31]

Zeng Y, Liu L, Huang D, Song D. Immortalized cell lines derived from dental/odontogenic tissue. Cell Tissue Res. 2023;393(1):1-15.

[32]

Gao Q, Wang L, Wang S, Huang B, Jing Y, Su J. Bone marrow mesenchymal stromal cells: identification, classification, and differentiation. Front Cell Dev Biol. 2022;9:787118-787128.

[33]

Zhang L, Luo W, Liu J, Xu M., Peng Q., Zou W., You J., Shu Y., Zhao P., Wagstaff W., Zhao G., Qin K., Haydon R. C., Luu H. H., Reid R. R., Bi Y., Zhao T., He T.C., Fu Z. Modeling lung diseases using reversibly immortalized mouse pulmonary alveolar type 2 cells (imPAC2). Cell Biosci 2022;12(1):159.

[34]

Luo W, Zhang L, Huang B, et al. BMP9-initiated osteogenic/odontogenic differentiation of mouse tooth germ mesenchymal cells (TGMCS) requires Wnt/β-catenin signalling activity. J Cell Mol Med. 2021;25(5):2666-2678.

[35]

Wu X, Li Z, Zhang H, et al. Modeling colorectal tumorigenesis using the organoids derived from conditionally immortalized mouse intestinal crypt cells (ciMICs). Genes Dis. 2021;8(6):814-826.

[36]

Maqsood MI, Matin MM, Bahrami AR, et al. Immortality of cell lines: challenges and advantages of establishment. Cell Biol Int. 2013;37(10):1038-1045.

[37]

Huang X, Wang F, Zhao C, et al. Dentinogenesis and tooth-alveolar bone complex defects in BMP9/GDF2 knockout mice. Stem Cells Dev. 2019;28(10):683-694.

[38]

Kang Q, Sun MH, Cheng H, et al. Characterization of the distinct orthotopic bone-forming activity of 14 BMPs using recombinant adenovirus-mediated gene delivery. Gene Ther. 2004;11(17):1312-1320.

[39]

Maisani M, Pezzoli D, Chassande O, Mantovani D. Cellularizing hydrogel-based scaffolds to repair bone tissue: how to create a physiologically relevant micro-environment? journal of. Tissue Eng. 2017;8:1-26.

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2024 The Author(s). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences.

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