Development of a Novel Perfusion Rotating Wall Vessel Bioreactor with Ultrasound Stimulation for Mass-Production of Mineralized Tissue Constructs

被引:6
作者
Cha, Jae Min [1 ,2 ]
Hwang, Yu-Shik [3 ,4 ]
Kang, Dong-Ku [5 ]
Lee, Jun [6 ]
Cooper, Elana S. [7 ]
Mantalaris, Athanasios [7 ]
机构
[1] Incheon Natl Univ, Coll Engn, Dept Mechatron Engn, 119 Acad Ro, Incheon 22012, South Korea
[2] Incheon Natl Univ, Res Inst Engn & Technol, 3D Stem Cell Bioengn Lab, Incheon 22012, South Korea
[3] Kyung Hee Univ, Sch Dent, Dept Maxillofacial Biomed Engn, Seoul 02447, South Korea
[4] Kyung Hee Univ, Sch Dent, Inst Oral Biol, Seoul 02447, South Korea
[5] Incheon Natl Univ, Res Inst Basic Sci, Dept Chem, Incheon 22012, South Korea
[6] Wonkwang Univ, Wonkwang Bone Regenerat Res Inst, Iksan 570749, South Korea
[7] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
关键词
Rotating wall vessel bioreactor; Perfusion; Stem cells; Low-intensity ultrasound; 3D mineralized tissue constructs; EMBRYONIC STEM-CELLS; INTENSITY PULSED ULTRASOUND; ENGINEERING BONE TISSUE; CULTURE-SYSTEM; BODY FORMATION; DIFFERENTIATION; CULTIVATION; EXPANSION; MOUSE; SUSPENSION;
D O I
10.1007/s13770-022-00447-3
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: As stem cells are considered a promising cell source for tissue engineering, many culture strategies have been extensively studied to generate in vitro stem cell-based tissue constructs. However, most approaches using conventional tissue culture plates are limited by the lack of biological relevance in stem cell microenvironments required for neotissue formation. In this study, a novel perfusion rotating wall vessel (RWV) bioreactor was developed for mass-production of stem cell-based 3D tissue constructs. Methods: An automated RWV bioreactor was fabricated, which is capable of controlling continuous medium perfusion, highly efficient gas exchange with surrounding air, as well as low-intensity pulsed ultrasound (LIPUS) stimulation. Embryonic stem cells encapsulated in alginate/gelatin hydrogel were cultured in the osteogenic medium by using our bioreactor system. Cellular viability, growth kinetics, and osteogenesis/mineralization were thoroughly evaluated, and culture media were profiled at real time. The in vivo efficacy was examined by a rabbit cranial defect model. Results: Our bioreactor successfully maintained the optimal culture environments for stem cell proliferation, osteogenic differentiation, and mineralized tissue formation during the culture period. The mineralized tissue constructs produced by our bioreactor demonstrated higher void filling efficacy in the large bone defects compared to the group implanted with hydrogel beads only. In addition, the LIPUS modules mounted on our bioreactor successfully reached higher mineralization of the tissue constructs compared to the groups without LIPUS stimulation. Conclusion: This study suggests an effective biomanufacturing strategy for mass-production of implantable mineralized tissue constructs from stem cells that could be applicable to future clinical practice.
引用
收藏
页码:739 / 754
页数:16
相关论文
共 57 条
[1]   Expansion of mouse embryonic stem cells on microcarriers [J].
Abranches, Elsa ;
Bekman, Evguenia ;
Henrique, Domingos ;
Cabral, Joaquim M. S. .
BIOTECHNOLOGY AND BIOENGINEERING, 2007, 96 (06) :1211-1221
[2]   The deformation of microscopic gel particles [J].
Andrei, DC ;
Briscoe, BJ ;
Luckham, PF ;
Williams, DR .
JOURNAL DE CHIMIE PHYSIQUE ET DE PHYSICO-CHIMIE BIOLOGIQUE, 1996, 93 (05) :960-976
[3]   Development of a perfusion fed bioreactor for embryonic stem cell-derived cardiomyocyte generation: Oxygen-mediated enhancement of cardiomyocyte output [J].
Bauwens, C ;
Yin, T ;
Dang, S ;
Peerani, R ;
Zandstra, PW .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 90 (04) :452-461
[4]   Adhesive contact deformation of a single microelastomeric sphere [J].
Briscoe, BJ ;
Liu, KK ;
Williams, DR .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1998, 200 (02) :256-264
[5]  
Calik M, 2014, EUR RESPIR J, V44
[6]   Improved development of human embryonic stem cell-derived embryoid bodies by stirred vessel cultivation [J].
Cameron, C. M. ;
Hu, Wei-Shou ;
Kaufman, Dan S. .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 94 (05) :938-948
[7]   Bioreactor systems are essentially required for stem cell bioprocessing [J].
Cha, Jae Min ;
Lee, Min-Young ;
Hong, Jongin .
PRECISION AND FUTURE MEDICINE, 2019, 3 (01) :19-23
[8]   Efficient scalable production of therapeutic microvesicles derived from human mesenchymal stem cells [J].
Cha, Jae Min ;
Shin, Eun Kyoung ;
Sung, Ji Hee ;
Moon, Gyeong Joon ;
Kim, Eun Hee ;
Cho, Yeon Hee ;
Park, Hyung Dal ;
Bae, Hojae ;
Kim, Jinseok ;
Bang, Oh Young .
SCIENTIFIC REPORTS, 2018, 8
[9]   Mesoderm Lineage 3D Tissue Constructs Are Produced at Large-Scale in a 3D Stem Cell Bioprocess [J].
Cha, Jae Min ;
Mantalaris, Athanasios ;
Jung, Sunyoung ;
Ji, Yurim ;
Bang, Oh Young ;
Bae, Hojae .
BIOTECHNOLOGY JOURNAL, 2017, 12 (09)
[10]  
CONAGHAN J, 1993, J REPROD FERTIL, V99, P87