Stem cell laden nano and micro collagen/PLGA bimodal fibrous patches for myocardial regeneration

Autor: Jung Hee Wee, Ki-Dong Yoo, Sung Bo Sim, Hyun Joo Kim, Han Joon Kim, Kyu Nam Park, Gee-Hee Kim, Mi Hyoung Moon, Su Jung You, Mi Yeon Ha, Dae Hyeok Yang, Heung Jae Chun, Jae Hoon Ko, Chun Ho Kim
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Biomaterials Research, Vol 26, Iss 1, Pp 1-17 (2022)
Druh dokumentu: article
ISSN: 2055-7124
DOI: 10.1186/s40824-022-00319-w
Popis: Abstract Background Although the use of cardiac patches is still controversial, cardiac patch has the significance in the field of the tissue engineered cardiac regeneration because it overcomes several shortcomings of intra-myocardial injection by providing a template for cells to form a cohesive sheet. So far, fibrous scaffolds fabricated using electrospinning technique have been increasingly explored for preparation of cardiac patches. One of the problems with the use of electrospinning is that nanofibrous structures hardly allow the infiltration of cells for development of 3D tissue construct. In this respect, we have prepared novel bi-modal electrospun scaffolds as a feasible strategy to address the challenges in cardiac tissue engineering . Methods Nano/micro bimodal composite fibrous patch composed of collagen and poly (D, L-lactic-co-glycolic acid) (Col/PLGA) was fabricated using an independent nozzle control multi-electrospinning apparatus, and its feasibility as the stem cell laden cardiac patch was systemically investigated. Results Nano/micro bimodal distributions of Col/PLGA patches without beaded fibers were obtained in the range of the 4-6% collagen concentration. The poor mechanical properties of collagen and the hydrophobic property of PLGA were improved by co-electrospinning. In vitro experiments using bone marrow-derived mesenchymal stem cells (BMSCs) revealed that Col/PLGA showed improved cyto-compatibility and proliferation capacity compared to PLGA, and their extent increased with increase in collagen content. The results of tracing nanoparticle-labeled as well as GFP transfected BMSCs strongly support that Col/PLGA possesses the long-term stem cells retention capability, thereby allowing stem cells to directly function as myocardial and vascular endothelial cells or to secrete the recovery factors, which in turn leads to improved heart function proved by histological and echocardiographic findings. Conclusion Col/PLGA bimodal cardiac patch could significantly attenuate cardiac remodeling and fully recover the cardiac function, as a consequence of their potent long term stem cell engraftment capability.
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