Message Board

Respected readers, authors and reviewers, you can add comments to this page on any questions about the contribution, review, editing and publication of this journal. We will give you an answer as soon as possible. Thank you for your support!

Name
E-mail
Phone
Title
Content
Verification Code
Volume 15 Issue 6
Nov.  2024
Turn off MathJax
Article Contents

CHEN Shumin, CHEN Yu, ZHAO Yuanjie, LIU Mengmeng. Isolation,culture and identification of mitral valve interstitial cells from Wuzhishan pig[J]. Journal of Tropical Biology, 2024, 15(6): 764-769. doi: 10.15886/j.cnki.rdswxb.20240049
Citation: CHEN Shumin, CHEN Yu, ZHAO Yuanjie, LIU Mengmeng. Isolation,culture and identification of mitral valve interstitial cells from Wuzhishan pig[J]. Journal of Tropical Biology, 2024, 15(6): 764-769. doi: 10.15886/j.cnki.rdswxb.20240049

Isolation,culture and identification of mitral valve interstitial cells from Wuzhishan pig

doi: 10.15886/j.cnki.rdswxb.20240049
  • Received Date: 2024-03-22
  • Rev Recd Date: 2024-04-08
  • Myxomatous mitral valve disease(MMVD) is one of the most common heart diseases in mammals,which can lead to heart failure and sudden death in clinical practice. The extracellular matrix remodeling caused by mitral stromal cells(MVICs) activation is the key pathological change in the development of MMVD.Therefore, this study intended to establish a separation and culture system for primary MVICs of Wuzhishan pig to obtain stable cultured MVICs, providing cell materials for in vitro research on MMVD. The results showed that the mitral valve cells of Wuzhishan pig isolated by the present method were CD31 negative and Vimentin positive, which were consistent with the characteristics of MVIC. Compared with the medium with different serum concentrations, the complete medium containing 10% FBS serum was more favorable to the proliferation activity of MVICs cells, and could support the stable culture of MVICs in vitro for at least 20 generations. The primary MVICs of Wuzhishan pig obtained in this study can provide an in vitro research platform for the study of the pathological mechanism of mitral valve disease and the further development of targeted drugs.
  • [1] O'BRIEN M J, BEIJERINK N J, WADE C M. Genetics of canine myxomatous mitral valve disease[J]. Anim Genet,2021, 52(4):409-421.
    [2] DELLING F N, VASAN R S. Epidemiology and pathophysiology of mitral valve prolapse:new insights into disease progression, genetics, and molecular basis[J]. Circulation, 2014, 129(21):2158-2170.
    [3] FOX P R. Pathology of myxomatous mitral valve disease in the dog[J]. J Vet Cardiol, 2012, 14(1):103-126.
    [4] KEENE B W, ATKINS C E, BONAGURA J D, et al.ACVIM consensus guidelines for the diagnosis and treatment of myxomatous mitral valve disease in dogs[J]. J Vet Intern Med, 2019, 33(3):1127-1140.
    [5] 宋光远,刘然,卢志南,等.功能性二尖瓣反流的治疗策略[J].临床心血管病杂志, 2022, 38(6):433-438.
    [6] TANG Q, MCNAIR A J, PHADWAL K, et al. The Role of Transforming Growth Factor-beta Signaling in Myxomatous Mitral Valve Degeneration[J]. Front Cardiovasc Med,2022, 9:872288.
    [7] PIERA-VELAZQUEZ S, LI Z, JIMENEZ S A. Role of endothelial-mesenchymal transition (EndoMT) in the pathogenesis of fibrotic disorders[J]. The American journal of pathology, 2011, 179(3):1074-1080.
    [8] MARKBY G, SUMMERS K M, MACRAE V E, et al.Myxomatous Degeneration of the Canine Mitral Valve:From Gross Changes to Molecular Events[J]. J Comp Pathol, 2017, 156(4):371-383.
    [9] 王希龙,欧江涛,黄礼光,等.海南五指山猪遗传多样性的微卫星分析[J].生物多样性, 2005, 13(1):20-26.
    [10] CAMACHO P, FAN H, LIU Z, et al. Large mammalian animal models of heart disease[J]. Journal of cardiovascular development and disease, 2016, 3(4):30.
    [11] ZHAO Y, XIANG L, LIU Y, et al. Atherosclerosis induced by a high-cholesterol and high-fat diet in the inbred strain of the Wuzhishan miniature pig[J]. Animal biotechnology, 2018, 29(2):110-118.
    [12] LIU M M, FLANAGAN T, LU C C, et al. Culture and characterisation of canine mitral valve interstitial and endothelial cells[J]. The Veterinary Journal, 2015, 204(1):32-39.
    [13] TAN K, MARKBY G, MUIRHEAD R, et al. Evaluation of canine 2D cell cultures as models of myxomatous mitral valve degeneration[J]. PLoS One, 2019, 14(8):e0221126.
    [14] WATABE T, TAKAHASHI K, PIETRAS K, et al. Roles of TGF-beta signals in tumor microenvironment via regulation of the formation and plasticity of vascular system[J].Semin Cancer Biol, 2023, 92:130-138.
    [15] LI Y, LUI K O, ZHOU B. Reassessing endothelial-tomesenchymal transition in cardiovascular diseases[J].Nat Rev Cardiol, 2018, 15(8):445-456.
    [16] BISCHOFF J. Endothelial-to-Mesenchymal Transition[J].Circ Res, 2019, 124(8):1163-1165.
    [17] TANG Q, MARKBY G R, MACNAIR A J, et al. TGFbeta-induced PI3K/AKT/mTOR pathway controls myofibroblast differentiation and secretory phenotype of valvular interstitial cells through the modulation of cellular senescence in a naturally occurring in vitro canine model of myxomatous mitral valve disease[J]. Cell Prolif, 2023,56(6):e13435.
    [18] HEANEY A M, BULMER B J, ROSS C R, et al. A technique for in vitro culture of canine valvular interstitial cells[J]. Journal of Veterinary Cardiology, 2009, 11(1):1-7.
    [19] SCHROEDER M E, GONZALEZ RODRIGUEZ A,SPECKL K F, et al. Collagen networks within 3D PEG hydrogels support valvular interstitial cell matrix mineralization[J]. Acta Biomater, 2021, 119:197-210.
    [20] WU S, LI Y, ZHANG C, et al. Tri-Layered and Gel-Like Nanofibrous Scaffolds with Anisotropic Features for Engineering Heart Valve Leaflets[J]. Adv Healthc Mater,2022, 11(10):e2200053.
    [21] BLEVINS T L, CARROLL J L, RAZA A M, et al. Phenotypic characterization of isolated valvular interstitial cell subpopulations[J]. The Journal of heart valve disease,2006, 15(6):815-822.
    [22] CONNELL P S, HAN R I, GRANDE-ALLEN K J. Differentiating the aging of the mitral valve from human and canine myxomatous degeneration[J]. J Vet Cardiol,2012, 14(1):31-45.
    [23] LIU A C, JOAG V R, GOTLIEB A I. The emerging role of valve interstitial cell phenotypes in regulating heart valve pathobiology[J]. Am J Pathol, 2007, 171(5):1407-1418.
  • 加载中
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Article views(20) PDF downloads(0) Cited by()

Proportional views
Related

Isolation,culture and identification of mitral valve interstitial cells from Wuzhishan pig

doi: 10.15886/j.cnki.rdswxb.20240049

Abstract: Myxomatous mitral valve disease(MMVD) is one of the most common heart diseases in mammals,which can lead to heart failure and sudden death in clinical practice. The extracellular matrix remodeling caused by mitral stromal cells(MVICs) activation is the key pathological change in the development of MMVD.Therefore, this study intended to establish a separation and culture system for primary MVICs of Wuzhishan pig to obtain stable cultured MVICs, providing cell materials for in vitro research on MMVD. The results showed that the mitral valve cells of Wuzhishan pig isolated by the present method were CD31 negative and Vimentin positive, which were consistent with the characteristics of MVIC. Compared with the medium with different serum concentrations, the complete medium containing 10% FBS serum was more favorable to the proliferation activity of MVICs cells, and could support the stable culture of MVICs in vitro for at least 20 generations. The primary MVICs of Wuzhishan pig obtained in this study can provide an in vitro research platform for the study of the pathological mechanism of mitral valve disease and the further development of targeted drugs.

CHEN Shumin, CHEN Yu, ZHAO Yuanjie, LIU Mengmeng. Isolation,culture and identification of mitral valve interstitial cells from Wuzhishan pig[J]. Journal of Tropical Biology, 2024, 15(6): 764-769. doi: 10.15886/j.cnki.rdswxb.20240049
Citation: CHEN Shumin, CHEN Yu, ZHAO Yuanjie, LIU Mengmeng. Isolation,culture and identification of mitral valve interstitial cells from Wuzhishan pig[J]. Journal of Tropical Biology, 2024, 15(6): 764-769. doi: 10.15886/j.cnki.rdswxb.20240049
Reference (23)

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return