You're using an outdated browser. Please upgrade to a modern browser for the best experience.
Myocardium Infarction: Comparison
View Latest Version
Please note this is a comparison between Version 2 by Vicky Zhou and Version 1 by Piyush Kumar Gupta.

Myocardium Infarction (MI) is one of the foremost cardiovascular diseases (CVDs) causing death worldwide, and its case numbers are expected to continuously increase in the coming years. Pharmacological interventions have not been at the forefront in ameliorating MI-related morbidity and mortality. Stem cell-based tissue engineering approaches have been extensively explored for their regenerative potential in the infarcted myocardium. Recent studies on microfluidic devices employing stem cells under laboratory set-up have revealed meticulous events pertaining to the pathophysiology of MI occurring at the infarcted site. This discovery also underpins the appropriate conditions in the niche for differentiating stem cells into mature cardiomyocyte-like cells and leads to engineering of the scaffold via mimicking of native cardiac physiological conditions. However, the mode of stem cell-loaded engineered scaffolds delivered to the site of infarction is still a challenging mission, and yet to be translated to the clinical setting.

  • myocardial infarction
  • stem cells
  • regeneration
  • biomaterial
  • cardiomyocytes
  • tissue engineering

1. Introduction

Cardiovascular disease, predominantly MI, is attributed the highest mortality rate worldwide [1]. Reduced contractility and function, irregular left ventricle remodeling, and uneven stress distribution in the heart muscle are among the complications occurring post-MI, eventually resulting in catastrophic heart failure. According to the American Heart Association (AHA)’s “Heart Disease and Stroke Statistics—2021”, the prevalence of CVD (including heart failure, hypertension, and stroke) in the US population is 49.2% in the age range of 20 years and above [2]. In 2014, 150,000 people died due to MI; thus an estimated approximately 14% of global death occurs mainly due to MI. Furthermore, MI survivors are also 15 times more likely to develop post-disease complications that lead to heart failure, and are prone to die sooner rather than later compared to the normal population [1]. Cardiac ischemia-related deaths have also ascended to the top of the list of causes of death in India, the United States, and Europe, apart from MI [1][3][4]. After MI incidence, male and female patients above 45 years of age have a lower life expectancy, of 8.2 and 5.5 years, respectively [1]. Socioeconomic burdens such as health care infrastructure and treatment costs (USD 11.5 billion) have made MI one of the top ten most expensive illnesses in the United States [1][5]. Researchers and clinicians around the world have been working extensively to reduce the global incidence of MI and develop significant cost-effective treatment strategies to reduce the mortality rate from MI.

The human heart is a complex organ composed of various types of cells such as cardiomyocytes (CM), fibroblasts, endothelial cells, valve interstitial cells, and resident cardiac stem cells. The cells of the heart are very active metabolically, as it physiologically requires adenosine tri-phosphate (ATP) for its function. Nonetheless, the heart lacks endogenous repair or regeneration potential, thus it remains devoid of regenerative capacity. Any defect in size or deficiency in cardiomyocyte numbers leads to life-threatening MI-related cardiovascular complications [6]. Currently, mitigation of CVDs by pharmaceutical drugs and other clinical practices have effectively improved the patient’s survival and quality of life after tissue damage [7]. However, this remains only a short-term solution of temporary duration; the permanent curative would be via heart transplant. Severe shortage of donor organs, post-graft complications, and the limited efficacy of pharmacological interventions has placed the emphasis on cell-loaded scaffold-based therapeutic approaches for cardiovascular complications (CVDs).

The emergence of cardiac tissue engineering (CTE) has not only given substantial hope for resolving or rescuing the damaged heart after MI but also for prompting the regeneration of the damaged myocardium, thus providing a permanent curative. The idea of CTE was first impelled in 1995 by in vitro-generated cardiac tissue obtained from embryonic chicken CMs. This further ushered in the prospect of new research areas around CTE, mainly idealised to translate the bench to bedside. CTE primarily aims to recapitulate the in vivo cardiac niche under in vitro conditions. Therefore, the long-term goals of CTE are considered the construction of in vitro-fabricated tissues for in vivo cardiac repair and regeneration, in vitro preclinical models for evaluation of drug toxicity, and disease models for understanding the development and pathophysiology of heart-related disorders [8]. With the global rise in CVD cases, it is essential to reinforce the treatment modalities for better disease management. In the current scenario, the previously mentioned CTE is considered as at the forefront; however, the conducting of numerous clinical trials is crucial in prioritizing CTE in clinical practice.

Delivery of an engineered scaffold loaded with stem cells, CM mitogens, or pharmacological molecules directly to the infarcted site via either the intra-coronary or intra-myocardial mode leads to the relatively prompt recovery of the infarcted tissue, followed by regeneration and regaining of functional significance. Still to be addressed are the current roadblocks to successive clinical utilization, such as an optimized protocol for stem cell-derived CMs and their source, biomaterials for CM cultures, as well as their delivery strategies [9]. Advanced delivery approaches using injectable or patch-based methods are recently gaining significant attention due to their complexity in design and versatility in application. The most advanced technology, using iPSC-derived CM-loaded microfluidic devices, has now been providing unprecedented opportunities to understand the mechanisms of MI development. This technology can also be employed to study the effects of drugs in the preclinical drug screening phase [10].

The recent technological advances in cardiac tissue engineering, for example, cell-based therapy and patch-based therapy, have been elucidated in Figure 1.

Cells 10 02538 g001

Figure 1. Schematic representation of various tissue engineering approaches for MI treatment. These approaches include hydrogel-based cell delivery (left hand corner), patch-based cell delivery (middle panel), and microfluidics-based drug screening (right corner) during the regenerative therapy of damaged heart tissue.

2. Recent Advances in Cardiac Tissue Engineering for the Management of Myocardium Infarction

2.1. Regenerative Therapy

Heart failure due to the progressive complications of MI mainly occurs due to the limited intrinsic regenerative potential of the myocardium. A left-ventricular assist device (LVAD), fixed internally to relieve the pressure on the heart left region, is the only available medication for the management of post-MI complications. This temporarily delays post MI complications; meanwhile, in such cases, a heart transplant can be the only permanent solution. However, the lack of organ donors has led researchers and clinicians to contemplate alternative therapies available immediately after MI for minimizing cardiomyocyte damage and thereby preventing subsequent heart failure. Under these conditions, cell-based therapy is ideal for repairing the initial injury, restoring lost cardiomyocytes, and preventing the development of a scar (which impairs cardiac function) (Figure 2). Many research groups are currently investigating the possibility of restoring cardiac function by replacing lost cardiomyocytes or via rejuvenating the resident cardiac stem cell population to counterbalance the lost CMs. Cell therapy has conventionally been a modest procedure in which cells are directly injected into the myocardium [11][12][13][14][15][16][17][18][19][20]. These cells may function in various ways, including differentiation into cardiomyocytes, support for endogenous regeneration, and/or protection of the affected cells. Several cell types have been investigated for their regenerative ability, each with its own set of benefits and side effects [13]; among these are mesenchymal stem cells, bone marrow cells, and cardiac progenitor cells. These have been shown to improve heart function in preclinical studies and are currently being studied in clinical trials [21]. Cell therapy using mesenchymal stem cells and bone marrow cells has been effective to some extent, but these cells are unable to differentiate into cardiomyocytes due to their restricted differentiation potential.
Cells 10 02538 g002
Figure 2. Illustration of stem cell-based regenerative medicine in MI treatment. Various stem cells like MSCs, ESCs, and iPSCs have been employed in MI treatment. Stem cells are delivered through engineered novel biomaterials (via encapsulation) that mimic the native niche. The stem cell-based regenerative therapy is beneficial to either replace the injured area or the whole organ.

2.2. Cell Based Therapy

In the tissue engineering and regeneration process, various types of cells are involved (Figure 3). Before using any cells, the key issues such as administration of immunosuppression and disease transmission to the host have to be addressed. Although autologous cell transplantation circumvents the use of immunosuppressants and holds a lower risk of disease transmission, the restricted supply hinders its application. Allogenic cells can also be used, but they require immunosuppression and pose a danger of disease transmission. Other disadvantages include the difficulty of collecting cells from donor sources, and of expanding their prior integration into the host. Furthermore, depending on the source of extraction (e.g., elderly persons or diabetic patients), autologous cells may have limited proliferation and differentiation [13][22][23]. Pluripotent stem cells such as embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) are cells that have the ability to self-renew and to give rise to any of the three primary germ cell layers, but not extra-embryonic tissues [24]. Studies employing stem cells in an animal model of cardiac injury and their outcomes have been summarized in Table 1.
Cells 10 02538 g003
Figure 3. Distinct cells of different origins which are used in the regenerative medicine depicted herein. Depending on the pluripotency, the transplanted cell types can differentiate into various other cells such as skeletal myoblasts, endothelial progenitor cells, chondrocytes, adipocytes, or cardiomyocytes.
Table 1. Description of the cells delivered to the heart by injection. This cell delivery approach has used various cell types including ESCs, iPSCs, MSCs, and CSCs.
Initial Cell Type Target Cell Type Composition of Delivery Vehicle Mode of Delivery Animal Models Outcomes Limitations References
iPSCs CMs Polyethylene glycol hydrogel Trans-epicardial MI in nude rats Increased infarct thickness and improved muscle content No donor cell engraftment was observed [25]
Mouse ESCs CMs PA-RGDS based gel Trans-epicardial Mice Engraftment and integration of mESC-CMs into host myocardium

improved cardiac function		 No information available on cardiac remodelling [12]
iPSCs CMs PBS solution Trans-epicardial Post-infarcted swine Enhanced angiogenesis, reduced apoptosis, and blunted cardiac remodelling No detailed information available on the engraftment of donor cell [26]
MSCs **** Self-assembling peptide hydrogels (3-D Matrix, Ltd.) Surface immobilization by spreading Lewis rats Augmented microvascular formation and reduced interstitial fibrosis No detailed information available on the engraftment of donor cell and CMs differentiation from MSC [27]
MSCs **** Si-HPMC Trans-epicardial Lewis rats Short-term recovery of ventricular function and attenuated mid-term remodelling No detailed information available on the engraftment of donor cell and CMs differentiation from MSC [28]
c-Kit overexpressing CSCs **** PBS solution Intracoronary Fischer 344 rats Preserved LV function and structure Increased cell dose was found to be harmful. Cell tracing or engraftment were not available in detail [28]
CSCs **** Matrigel and dimethylpolysiloxane mixture gel Trans-epicardial NOD-SCID mice Improved long-term retention of CSCs, cardiac structure and function Cell tracing or engraftment were not available [29]
**** Studies were carried out to observe the improvement in cardiac function. The available report did not present specifics on the engraftment and in situ differentiation of delivered cells to mature CMs.

2.3. Microfluidics Based MI Research

Microfluidics deals with the handling of very small volumes of liquid, typically in a length scale of a few micrometers. Since its development in the early 1980s, it has been discovered to be an effective tool with a wide range of applications, from inkjet printers to LOC systems. Over the last two decades, microfluidics has been used in many biological fields such as genomics and proteomics, point-of-care diagnostic systems, biohazard detection, and more. Its recent developments have enabled tissue engineering research to be done in a more cost-effective and highly sensitive way. Research related to MI has been explored using microfluidic devices as it becomes feasible to create a 3D tissue structure and study it in a dynamic condition mimicking both healthy and pathophysiological states of the heart [30]. Microfluidics emerged from the conventional silicon and glass micro-machining process. With the advent of photo-lithography and other BioMEMS fabrication techniques, the whole process has become more user-friendly. The range of materials used for fabrication is vast, and includes different polymers, silicon, silicon-based materials, metals, etc. Materials are selected based on properties like rigidity or flexibility, optical transparency, biocompatibility, and reactivity to reagents. PDMS is a common material used for microfluidics because of properties like high oxygen permeability, ease of fabrication, and biocompatibility. As cell behavior also depends upon the topography of its environment, the surface chemistry of these materials plays a vital role in cell culture. The biocompatibility of these surfaces can also be increased via processes such as plasma deposition [31]. Cell culture work close to the physiologic environment is possible in a microfluidic chip, with better control over the process parameters. Such work has led to the use of human samples for research and reduced dependence on animal models for drug discovery and therapeutics. The small sample size requirement for microfluidic devices helps in handling costly samples and reagents. Miniaturized 3D tissue models can produce better studies on physiological systems and their behavior for toxicity assay studies. The flow conditions in a microfluidic device are very much essential in cellular studies, as the physiological environment is seldom static. The microfluidic LOC device has also been designed to easily generate different physiological, mechanical, or electrical forces on the culture, which are complicated in macro bioreactors. The whole system can be designed and optimized through different available computational software (e.g., Comsol, Ansys, etc.). These devices can also be linked to external analytical devices in order to study real-time cell behavior (Figure 54) [32]. Cells 10 02538 g005 Figure 54. Steps in microfluidic cardiac model generation—(a) Selection of cells and extracellular matrix are performed based on the physiology to be studied; (b) this is followed by design of the chip through different computational software to achieve the desired flow contours; (c) based on the design, the device is fabricated by various microfabrication procedures (the most common being photolithography; the steps of which are 1. spin coating of clean silicon wafer, 2. UV exposure with a mask, 3. dissolution of unwanted resist with developer solution to generate the master pattern, 4. PDMS mold creation from the master pattern, 5. punching of required inlet and outlet holes in the PDMS mold, and 6. bonding of the PDMS mold with a glass plate or another PDMS slab to close the device); (d) introduction of cell-laden hydrogel into the device for 3D culture (its selection is based on the mechanical properties needed for the micro tissue under study; (e) completion of the electrical circuit required for stimulation of the cardiac cells; (f) integration of the device with external circuitry and pumping mechanism for seamless operation of the chip [33][34][35][36].

3. Future Directions

In spite of technological advances in the study of cell biology, cellular behavior, and the pathophysiology of MI, there are many of unconnected questions that have to be solved in order to achieve a more efficient and effective stem cell-based therapy for MI. Understandably, no single therapeutic approach will suit all, but to do what can be done to narrow down stem cells, delivery approaches, and biomaterials to the minimal and most efficient formation is the major challenge requiring a detailed and thorough exploration. However, it is still not clear which stem cell is ideal for treating acute or chronic MI. Which mode of delivery is best or better than others, and which biomaterial is most suitable for stem cell delivery to the infarcted region? Many clinical trials have been completed so far, and many will be conducted in the upcoming years. However, a clear strategy has to be evolved in order to find the best combination of stem cells, delivery approach, and biomaterial components to meet the requirement in most cases, if not all.
Microfluidics is another major research area that has helped in the resolution of many complicated questions such as the selection of biomaterials and the mechanisms involved in transplanted stem cell-mediated MI heart regeneration, as well as the basic pathophysiology of MI. Most importantly, microfluidics can be used to more efficiently understand the angiogenesis process and the therapeutic interventions required to increase the vasculature density in the infarcted region. Eventually, it could help to improve the functionality of the infarcted heart.
Stem cell delivery to the infarcted myocardium has become indispensable for regenerating the heart so as to regain functionality similar to native cardiac function. To this end, various stem cells have been used for delivery to the infarcted heart. Processes used include direct injection into the myocardium and using a 3D biocompatible scaffold (commonly called a patch) to deliver a higher dose of cells with uniform distribution across the infarcted region. Several mechanisms have been documented where either the transplanted stem cells differentiate into functional CMs and integrate with the heart to improve cardiac function or act through a paracrine manner to induce the regeneration of CMs, increase neovascularization, reduce scar formation, increase ventricular function and decrease remodeling of the myocardium. Hence, the forthcoming mechanistic studies on exosomes and direct tagging of stem cells for monitoring the homing studies after transplantation may further result in translating bench studies to the bedside.

References

  1. Benjamin, E.J.; Blaha, M.J.; Chiuve, S.E.; Cushman, M.; Das, S.R.; Deo, R.; De Ferranti, S.D.; Floyd, J.; Fornage, M.; Gillespie, C.; et al. Heart Disease and Stroke Statistics’ 2017 Update. Circulation 2017, 135, e146–e603.
  2. Virani, S.S.; Alonso, A.; Aparicio, H.J.; Benjamin, E.J.; Bittencourt, M.S.; Callaway, C.W.; Carson, A.P.; Chamberlain, A.M.; Cheng, S.; Delling, F.N.; et al. Heart Disease and Stroke Statistics—2021. Circulation 2021, 143, 254–743.
  3. Prabhakaran, D.; Jeemon, P.; Roy, A. Cardiovascular Diseases in India: Current Epidemiology and Future Directions. Circulation 2016, 133, 1605–1620.
  4. Timmis, A.; Townsend, N.; Gale, C.P.; Torbica, A.; Lettino, M.; Petersen, S.E.; Mossialos, E.A.; Maggioni, A.P.; Kazakiewicz, D.; May, H.T.; et al. European society of cardiology: Cardiovascular disease statistics 2019. Eur. Heart J. 2020, 41, 12–85.
  5. Pfuntner, A.; Wier, L.M.; Stocks, C. Most Frequent Conditions in U.S. Hospitals, 2011: Statistical Brief#162; Agency for Healthcare Research and Quality: Rockville, MD, USA, 2006.
  6. Frangogiannis, N.G. Pathophysiology of myocardial infarction. Compr. Physiol. 2015, 5, 1841–1875.
  7. Tonsho, M.; Michel, S.; Ahmed, Z.; Alessandrini, A.; Madsen, J.C. Heart transplantation: Challenges facing the field. Cold Spring Harb. Perspect. Med. 2014, 4, a015636.
  8. Feric, N.T.; Radisic, M. Maturing human pluripotent stem cell-derived cardiomyocytes in human engineered cardiac tissues. Adv. Drug Deliv. Rev. 2016, 96, 110–134.
  9. Vunjak-Novakovic, G.; Tandon, N.; Godier, A.; Maidhof, R.; Marsano, A.; Martens, T.P.; Radisic, M. Challenges in cardiac tissue engineering. Tissue Eng. Part B Rev. 2020, 16, 169–187.
  10. Cahill, T.J.; Choudhury, R.P.; Riley, P.R. Heart regeneration and repair after myocardial infarction: Translational opportunities for novel therapeutics. Nat. Rev. Drug Discov. 2017, 16, 699–717.
  11. Bagno, L.; Hatzistergos, K.E.; Balkan, W.; Hare, J.M. Mesenchymal Stem Cell-Based Therapy for Cardiovascular Disease: Progress and Challenges. Mol. Ther. 2018, 26, 1610–1623.
  12. Ban, K.; Park, H.-J.; Kim, S.; Andukuri, A.; Cho, K.-W.; Hwang, J.W.; Cha, H.J.; Kim, S.Y.; Kim, W.-S.; Jun, H.-W.; et al. Cell Therapy with Embryonic Stem Cell-Derived Cardiomyocytes Encapsulated in Injectable Nanomatrix Gel Enhances Cell Engraftment and Promotes Cardiac Repair. ACS Nano 2014, 8, 10815–10825.
  13. Cambria, E.; Pasqualini, F.S.; Wolint, P.; Günter, J.; Steiger, J.; Bopp, A.; Hoerstrup, S.P.; Emmert, M.Y. Translational cardiac stem cell therapy: Advancing from first-generation to next-generation cell types. Npj Regen. Med. 2017, 2, 1–9.
  14. Chetty, S.S.; Praneetha, S.; Vadivel Murugan, A.; Varthana, K.; Verma, R.S. Human Umbilical Cord Wharton’s Jelly-Derived Mesenchymal Stem Cells Labeled with Mn2+ and Gd3+ Co-Doped CuInS2-ZnS Nanocrystals for Multimodality Imaging in a Tumor Mice Model. ACS Appl. Mater. Interfaces 2020, 12, 3415–3429.
  15. Behfar, A.; Perez-Terzic, C.; Faustino, R.S.; Arrell, D.K.; Hodgson, D.M.; Yamada, S.; Puceat, M.; Niederländer, N.; Alekseev, A.E.; Zingman, L.V.; et al. Cardiopoietic programming of embryonic stem cells for tumor-free heart repair. J. Exp. Med. 2007, 19, 405–420.
  16. Kim, J.; Shapiro, L.; Flynn, A. The clinical application of mesenchymal stem cells and cardiac stem cells as a therapy for cardiovascular disease. Pharmacology 2015, 151, 8–15.
  17. Ji, L.L.; Long, X.F.; Tian, H.; Liu, Y.F. Effect of transplantation of bone marrow stem cells on myocardial infarction size in a rabbit model. World J. Emerg. Med. 2013, 4, 304–310.
  18. Roura, S.; Gálvez-Montón, C.; Mirabel, C.; Vives, J.; Bayes-Genis, A. Mesenchymal stem cells for cardiac repair: Are the actors ready for the clinical scenario? Stem Cell Res. Ther. 2017, 8, 1–11.
  19. Shen, X.; Pan, B.; Zhou, H.; Liu, L.; Lv, T.; Zhu, J.; Huang, X.; Tian, J. Differentiation of mesenchymal stem cells into cardiomyocytes is regulated by miRNA-1-2 via WNT signaling pathway. J. Biomed. Sci. 2017, 24, 1–8.
  20. Tang, J.N.; Cores, J.; Huang, K.; Cui, X.L.; Luo, L.; Zhang, J.Y.; Li, T.S.; Qian, L.; Cheng, K. Concise Review: Is Cardiac Cell Therapy Dead? Embarrassing Trial Outcomes and New Directions for the Future. Stem Cells Transl. Med. 2018, 7, 354–359.
  21. Tompkins, B.A.; Balkan, W.; Winkler, J.; Gyöngyösi, M.; Goliasch, G.; Fernández-Avilés, F.; Hare, J.M. Preclinical Studies of Stem Cell Therapy for Heart Disease. Circ. Res. 2018, 122, 1006–1020.
  22. Chen, Z.; Chen, L.; Zeng, C.; Wang, W.E. Functionally improved mesenchymal stem cells to better treat myocardial infarction. Stem Cells Int. 2018, 2018, 7045245.
  23. Verma, R.S. Recent Advances in Induced Pluripotent Stem Cell (iPSC) based Therapeutics. J. Stem Cell Res. Ther. 2017, 16, 115–130.
  24. Xu, J.-Y.; Cai, W.-Y.; Tian, M.; Liu, D.; Huang, R.-C. Stem cell transplantation dose in patients with acute myocardial infarction: A meta-analysis. Chronic Dis. Transl. Med. 2016, 2, 92–101.
  25. Chow, A.; Stuckey, D.J.; Kidher, E.; Rocco, M.; Jabbour, R.J.; Mansfield, C.A.; Darzi, A.; Harding, S.E.; Stevens, M.M.; Athanasiou, T. Human Induced Pluripotent Stem Cell-Derived Cardiomyocyte Encapsulating Bioactive Hydrogels Improve Rat Heart Function Post Myocardial Infarction. Stem Cell Rep. 2017, 9, 1415–1422.
  26. Song, G.; Li, X.; Shen, Y. Qian, L.; Kong, X.; Chen, M.; Cao, K.; Zhang, F. Transplantation of iPSc Restores Cardiac Function by Promoting Angiogenesis and Ameliorating Cardiac Remodeling in a Post-infarcted Swine Model. Cell Biochem. Biophys. 2015, 71, 1463–1473.
  27. Ichihara, Y.; Kaneko, M.; Yamahara, K.; Koulouroudias, M.; Sato, N.; Uppal, R.; Yamazaki, K.; Saito, S.; Suzuki, K. Self-assembling peptide hydrogel enables instant epicardial coating of the heart with mesenchymal stromal cells for the treatment of heart failure. Biomaterials 2018, 154, 12–23.
  28. Mathieu, E.; Lamirault, G.; Toquet, C.; Lhommet, P.; Rederstorff, E.; Sourice, S.; Biteau, K.; Hulin, P.; Forest, V.; Weiss, P.; et al. Intramyocardial delivery of mesenchymal stem cell-seeded hydrogel preserves cardiac function and attenuates ventricular remodeling after myocardial infarction. PLoS ONE 2012, 7, e51991.
  29. Mayfield, A.E.; Tilokee, E.L.; Latham, N.; McNeill, B.; Lam, B.-K.; Ruel, M.; Suuronen, E.J.; Courtman, D.W.; Stewart, D.J.; Davis, D.R. The effect of encapsulation of cardiac stem cells within matrix-enriched hydrogel capsules on cell survival, post-ischemic cell retention and cardiac function. Biomaterials 2014, 35, 133–142.
  30. Inamdar, N.K.; Borenstein, J.T. Microfluidic cell culture models for tissue engineering. Curr. Opin. Biotechnol. 2011, 22, 681–689.
  31. Ni, M.; Tong, W.H.; Choudhury, D.; Rahim, N.A.A.; Iliescu, C.; Yu, H. Cell culture on MEMS platforms: A review. Int. J. Mol. Sci. 2009, 10, 5411–5441.
  32. Whitesides, G.M. The origins and the future of microfluidics. Nature 2006, 442, 368–373.
  33. Kobuszewska, A.; Tomecka, E.; Zukowski, K.; Jastrzebska, E.; Chudy, M.; Dybko, A.; Renaud, P.; Brzozka, Z. Heart-on-a-Chip: An Investigation of the Influence of Static and Perfusion Conditions on Cardiac (H9C2) Cell Proliferation, Morphology, and Alignment. SLAS Technol. Transl. Life Sci. Innov. 2017, 22, 536–546.
  34. Qiao, Y.; Dong, Q.; Li, B.; Obaid, S.; Miccile, C.; Yin, R.T.; Talapatra, T.; Lin, Z.; Li, S.; Li, Z.; et al. Multiparametric slice culture platform for the investigation of human cardiac tissue physiology. Prog. Biophys. Mol. Biol. 2019, 144, 139–150.
  35. Visone, R.; Talò, G.; Occhetta, P.; Cruz-moreira, D.; Lopa, S.; Pappalardo, O.A.; Redaelli, A.; Moretti, M.; Rasponi, M. A microscale biomimetic platform for generation and electro-mechanical stimulation of 3D cardiac microtissues. APL Bioeng. 2018, 2, 046102.
  36. Visone, R.; Ugolini, G.S.; Vinarsky, V.; Penati, M.; Redaelli, A.; Forte, G.; Rasponi, M. A Simple Vacuum-Based Microfluidic Technique to Establish High-Throughput Organs-On-Chip and 3D Cell Cultures at the Microscale. Adv. Mater. Technol. 2019, 4, 1–8.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)
Academic Video Service
Feedback