A three-dimensional culture system for generating cardiac spheroids composed of cardiomyocytes, endothelial cells, smooth-muscle cells, and cardiac fibroblasts derived from human induced-pluripotent stem cells

被引:27
|
作者
Kahn-Krell, Asher [1 ,2 ]
Pretorius, Danielle [1 ,2 ]
Guragain, Bijay [1 ,2 ]
Lou, Xi [1 ,2 ]
Wei, Yuhua [1 ,2 ]
Zhang, Jianhua [3 ,4 ]
Qiao, Aijun [1 ,2 ]
Nakada, Yuji [1 ,2 ]
Kamp, Timothy J. [3 ,4 ,5 ]
Ye, Lei [1 ,2 ]
Zhang, Jianyi [1 ,2 ,6 ]
机构
[1] Univ Alabama Birmingham, Sch Med, Dept Biomed Engn, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Sch Engn, Birmingham, AL 35294 USA
[3] Univ Wisconsin Madison, Sch Med & Publ Hlth, Dept Med, Madison, WI USA
[4] Univ Wisconsin Madison, Stem Cell & Regenerat Med Ctr, Madison, WI USA
[5] Univ Wisconsin Madison, Sch Med & Publ Hlth, Dept Cell & Regenerat Biol, Madison, WI USA
[6] Univ Alabama Birmingham, Dept Med Cardiovasc Dis, Birmingham, AL 35233 USA
关键词
pluripotent stem cell; cardiomyocyte; suspension culture; maturation; organoids; biomanufacturing; MYOCARDIAL-INFARCTION; IMPROVE RECOVERY; HIGHLY EFFICIENT; MATURATION; DIFFERENTIATION; MICROTISSUES; MATRIX; INJURY; MODEL; MODULATION;
D O I
10.3389/fbioe.2022.908848
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cardiomyocytes (CMs), endothelial cells (ECs), smooth-muscle cells (SMCs), and cardiac fibroblasts (CFs) differentiated from human induced-pluripotent stem cells (hiPSCs) are the fundamental components of cell-based regenerative myocardial therapy and can be used as in-vitro models for mechanistic studies and drug testing. However, newly differentiated hiPSC-CMs tend to more closely resemble fetal CMs than the mature CMs of adult hearts, and current techniques for improving CM maturation can be both complex and labor-intensive. Thus, the production of CMs for commercial and industrial applications will require more elementary methods for promoting CM maturity. CMs tend to develop a more mature phenotype when cultured as spheroids in a three-dimensional (3D) environment, rather than as two-dimensional monolayers, and the activity of ECs, SMCs, and CFs promote both CM maturation and electrical activity. Here, we introduce a simple and reproducible 3D-culture-based process for generating spheroids containing all four cardiac-cell types (i.e., cardiac spheroids) that is compatible with a wide range of applications and research equipment. Subsequent experiments demonstrated that the inclusion of vascular cells and CFs was associated with an increase in spheroid size, a decline in apoptosis, an improvement in sarcomere maturation and a change in CM bioenergetics.
引用
收藏
页数:18
相关论文
共 50 条
  • [1] Three-dimensional cardiac microtissues composed of cardiomyocytes and endothelial cells co-differentiated from human pluripotent stem cells
    Giacomelli, Elisa
    Bellin, Milena
    Sala, Luca
    Van Meer, Berend J.
    Tertoolen, Leon G. J.
    Orlova, Valeria V.
    Mummery, Christine L.
    DEVELOPMENT, 2017, 144 (06): : 1008 - 1017
  • [2] Differentiation of Human Induced-Pluripotent Stem Cells into Smooth-Muscle Cells: Two Novel Protocols
    Yang, Libang
    Geng, Zhaohui
    Nickel, Thomas
    Johnson, Caitlin
    Gao, Lin
    Dutton, James
    Hou, Cody
    Zhang, Jianyi
    PLOS ONE, 2016, 11 (01):
  • [3] Component Currents of Cardiac Human Cardiomyocytes Derived from Induced Pluripotent Stem Cells
    Lis, Agniezka
    Cimato, Thomas J.
    Bett, Glenna C. L.
    Rasmusson, Randall L.
    Morales, Michael J.
    BIOPHYSICAL JOURNAL, 2012, 102 (03) : 674A - 674A
  • [4] Hypoimmunogenic Human Induced Pluripotent Stem Cells Derived Cardiomyocytes for Cardiac Regeneration
    Liu, Yen-Wen
    Fang, I-Hsien
    Wang, Saprina P.
    CIRCULATION, 2022, 146
  • [5] Development of Innovate Drug Screening System Using Three Dimensional Cardiac Tissues Combined With Cardiomyocytes Derived From Human Induced Pluripotent Stem Cells and Cardiac Component Cells.
    Takeda, Maki
    Miyagawa, Shigeru
    Ito, Emiko
    Harada, Akima
    Mochizuki-Oda, Noriko
    Akashi, Mitsuru
    Sawa, Yoshiki
    CIRCULATION, 2018, 138
  • [6] Engineered Human Cardiac Tissue from Skeletal Muscle Derived Cells and Induced Pluripotent Stem Cell Derived Cardiomyocytes
    Tobita, Kimimasa
    Tchao, Jason S.
    Kim, Jong
    Lin, Bo
    Huard, Johnny
    Salama, Guy
    Yang, Lei
    CIRCULATION RESEARCH, 2012, 111 (04)
  • [7] Transplantation of Human Induced Pluripotent Stem Cells Derived Cardiac Cells for Cardiac Repair
    Ye, Lei
    Xiong, Qiang
    Zhang, Pengyuan
    Lepley, Mike
    Swingen, Cory
    Zhang, Jianhua
    Kamp, Timothy J.
    Kaufman, Dan
    Zhang, Jianyi
    CIRCULATION, 2012, 126 (21)
  • [8] Elastin Mediated Smooth Muscle Cell Differentiation in Human Embryonic Stem Cells and Induced-Pluripotent Stem Cells
    Kinnear, Caroline
    Hinek, Aleksander
    Pour, Maryam Nia
    Mahmut, Naila
    Wang, Yanting
    Chang, Wing Y.
    Ellis, James
    Keller, Gordon
    Stanford, William L.
    Mital, Seema
    CIRCULATION, 2010, 122 (21)
  • [9] Generating Injectable Vascularized Cardiomyocytes Derived From Human Induced Pluripotent Stem Cells
    Aoyama, Junya
    Sokol, Morgan
    Zhu, Anthony
    Cao, Fang
    Gil, Eun S.
    Aleksi, Elton
    Garbern, Jessica
    Elwell, Hannah
    Barrera, Irving
    Lee, Richard T.
    CIRCULATION RESEARCH, 2023, 133
  • [10] Electrical Stimulation for Cardiac Differentiation and Maturation of Cardiomyocytes Derived from Human Induced Pluripotent Stem Cells
    Hernandez, D.
    Sivakumaran, P.
    Millard, R.
    Wong, R. C.
    Hung, S. S.
    Crombie, D.
    Pebay, A.
    Shepherd, R. K.
    Dusting, G. J.
    Lim, S. Y.
    TISSUE ENGINEERING PART A, 2015, 21 : S249 - S249