Table 1.
Aspects of human cardiac physiology and disease in organs-on-chips | ||
---|---|---|
Cardiac physiology | Defined 3D tissue organization | 43 , 48 , 61 , 62 , 64 , 135 |
Force of contraction | 51 , 54 , 130 , 135 | |
Electrophysiology | 43 , 46 , 57 , 62 , 64 , 65 , 67 , 135 | |
Cardiac-vascular interactions | 44 , 46 , 62 , 135 | |
Body-on-chip approach | 54 , 130 , 135 | |
Cardiac disease and toxicity | Hypertrophy | 61 |
Arrhythmia | 47 , 49 | |
Ischaemia | 67 | |
Fibrosis (e.g. fibroblast proliferation, collagen deposition, and valve calcification) | 47 , 49 | |
Inflammation | 46 , 135 | |
Cardiotoxicity & Pharmacology | 43 , 44 , 46 , 51 , 54 , 61 , 62 , 64 , 65 , 130 , 135 |
The selection criteria employed in this table were that the devices used in the study could be considered a heart-on-a-chip device, i.e. a microfluidic device where the microenvironment of the cells or tissue in culture can be controlled and/or be stimulated mechanically and/or electrically. Platforms where constructs are cultured in well-plates or make use of spheroid technology were not considered due to the lack of their microfluidic character, which is seen as a requirement for organs-on-chips.