Cardiac-derived extracellular matrix: A decellularization protocol for heart regeneration

被引:6
|
作者
Belviso, Immacolata [1 ]
Sacco, Anna Maria [1 ]
Cozzolino, Domenico [1 ]
Nurzynska, Daria [2 ]
Di Meglio, Franca [1 ]
Castaldo, Clotilde [1 ]
Romano, Veronica [1 ]
机构
[1] Univ Naples Federico II, Dept Publ Hlth, Naples, Italy
[2] Univ Salerno, Scuola Med Salernitana, Dept Med Surg & Dent, Baronissi, Italy
来源
PLOS ONE | 2022年 / 17卷 / 10期
关键词
INFARCTION; SCAFFOLDS;
D O I
10.1371/journal.pone.0276224
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extracellular matrix (ECM) is a fundamental component of the heart, guiding vital cellular processes during organ homeostasis. Most cardiovascular diseases lead to a remarkable remodeling of the ECM, accompanied by the formation of a fibrotic tissue that heavily compromises the heart function. Effective therapies for managing fibrosis and promoting physiological ECM repair are not yet available. The production of a decellularized extracellular matrix (d-ECM) serving as a three-dimensional and bioactive scaffold able to modulate cellular behavior and activities is considered crucial to achieve a successful regeneration. The protocol represents a step-by-step method to obtain a decellularized cardiac matrix through the combination of sodium dodecyl sulphate (SDS) and Triton X-100. Briefly, cardiac samples obtained from left ventricles of explanted, pathological human hearts were dissected and washed to remove residual body fluids. Samples were then snap-frozen and sliced by a cryostat into 350 mu m thick sections. The sections obtained were decellularized using a solution containing 1% Triton X-100 and 1% SDS in combination, for 24 hours, until observing the color change from brownish-red to translucent-white. As a result, the protocol shows efficiency in preserving ECM architecture and protein composition during the whole process, suggesting that it is worthwhile, highly reproducible and produces a well- preserved decellularized extracellular matrix from cardiac samples. Notwithstanding, some limitations need to be addressed, such as the risk for microbial contamination and the unpredictable trend of the protocol when applied to decellularize samples other than myocardium, vessels, or skin. These issues require antibiotics mixture supplement during the procedure followed by UV sterilization, and appropriate adjustments for a tissue-specific utilization, respectively. The protocol is intended to produce a cardiac d-ECM for cell settlement, representing the ideal scaffold for tissue engineering purposes.
引用
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页数:10
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