Cell Therapy in the Heart: Cell Production, Transplantation, and Applications

2003 ◽  
pp. 73-81
Author(s):  
Kevin S. Cahill ◽  
Catalin Toma ◽  
Mark F. Pittenger ◽  
Paul D. Kessler ◽  
Barry J. Byrne
2012 ◽  
Vol 16 (3) ◽  
pp. 636-647 ◽  
Author(s):  
Peifeng Jin ◽  
Enshi Wang ◽  
Ye-huan Wang ◽  
Weicong Huang ◽  
Wenan Kuang ◽  
...  

Biomaterials ◽  
2020 ◽  
Vol 230 ◽  
pp. 119627 ◽  
Author(s):  
Ruoyu Chen ◽  
Ling Li ◽  
Lu Feng ◽  
Yixue Luo ◽  
Mingen Xu ◽  
...  
Keyword(s):  

2021 ◽  
pp. 151-190
Author(s):  
Yazan M. N. Kalou ◽  
Ammar S. A. Hashemi ◽  
Rayan M. Joudeh ◽  
Beatrice Aramini ◽  
Khawaja Husnain Haider

2021 ◽  
Vol 10 (8) ◽  
Author(s):  
Junlang Li ◽  
Shiqi Hu ◽  
Dashuai Zhu ◽  
Ke Huang ◽  
Xuan Mei ◽  
...  

Abstract In the past decades, numerous preclinical studies and several clinical trials have evidenced the feasibility of cell transplantation in treating heart diseases. Over the years, different delivery routes of cell therapy have emerged and broadened the width of the field. However, a common hurdle is shared by all current delivery routes: low cell retention. A myriad of studies confirm that cell retention plays a crucial role in the success of cell‐mediated cardiac repair. It is important for any delivery route to maintain donor cells in the recipient heart for enough time to not only proliferate by themselves, but also to send paracrine signals to surrounding damaged heart cells and repair them. In this review, we first undertake an in‐depth study of primary theories of cell loss, including low efficiency in cell injection, “washout” effects, and cell death, and then organize the literature from the past decade that focuses on cell transplantation to the heart using various cell delivery routes, including intracoronary injection, systemic intravenous injection, retrograde coronary venous injection, and intramyocardial injection. In addition to a recapitulation of these approaches, we also clearly evaluate their strengths and weaknesses. Furthermore, we conduct comparative research on the cell retention rate and functional outcomes of these delivery routes. Finally, we extend our discussion to state‐of‐the‐art bioengineering techniques that enhance cell retention, as well as alternative delivery routes, such as intrapericardial delivery. A combination of these novel strategies and more accurate assessment methods will help to address the hurdle of low cell retention and boost the efficacy of cell transplantation to the heart.


Author(s):  
W.G. Wier

A fundamentally new understanding of cardiac excitation-contraction (E-C) coupling is being developed from recent experimental work using confocal microscopy of single isolated heart cells. In particular, the transient change in intracellular free calcium ion concentration ([Ca2+]i transient) that activates muscle contraction is now viewed as resulting from the spatial and temporal summation of small (∼ 8 μm3), subcellular, stereotyped ‘local [Ca2+]i-transients' or, as they have been called, ‘calcium sparks'. This new understanding may be called ‘local control of E-C coupling'. The relevance to normal heart cell function of ‘local control, theory and the recent confocal data on spontaneous Ca2+ ‘sparks', and on electrically evoked local [Ca2+]i-transients has been unknown however, because the previous studies were all conducted on slack, internally perfused, single, enzymatically dissociated cardiac cells, at room temperature, usually with Cs+ replacing K+, and often in the presence of Ca2-channel blockers. The present work was undertaken to establish whether or not the concepts derived from these studies are in fact relevant to normal cardiac tissue under physiological conditions, by attempting to record local [Ca2+]i-transients, sparks (and Ca2+ waves) in intact, multi-cellular cardiac tissue.


2006 ◽  
Vol 175 (4S) ◽  
pp. 474-474
Author(s):  
Akira Joraku ◽  
Toshihiko Machiguchi ◽  
James J. Yoo ◽  
Anthony Atala
Keyword(s):  

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