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This cross-journal collection on “Microphysiological Systems” is a collaboration between Nature Communications, Communications Biology, Communications Engineering and Scientific Reports. Microphysiological Systems feature the culture of cells, tissues or organoids inside of biomimetic microfluidic devices that aim to recapitulate the circulation and interconnection between different organs found within the human body. These platforms modeling (patho)physiological processes promise to revolutionize basic research as well as drug development and screening, while enabling personalized medicine and reducing our reliance on animal experiments. Within this field, we look forward to seeing submissions on the sub-topics of, but not exclusively on, Engineering Advances, Modeling Biological Phenomena, and Modelling Disease & Drug Testing.
Leendert-Jan W. Ligtenberg and colleagues report an X-ray guided platform for the wireless teleoperation of hemocompatible, untethered magnetic robots. The approach will enable clinicians to reach and treat vascular diseases within the body where alternative tethered flexible surgical instruments offer more limited control.
Nidhi Sinha, Haowen Yang and colleagues report a microfluidic large-scale integration chip to probe temporal single-cell signalling networks via the delivery of patterns of input signalling molecules. The researchers use their device to investigate drug-induced cancer cell apoptosis and single cell transcription (STAT-1) protein signalling dynamics.
The functional heterogeneity of autophagy in endothelial cells during angiogenesis remains incompletely understood. Here, the authors apply a 3D angiogenesis-on-a-chip coupled with single-cell RNA sequencing to find distinct autophagy functions in two different endothelial cell populations during angiogenic sprouting.
Nguyen and colleagues report a microfluidic platform with a ladder shaped design which identifies bacterial susceptibility to antibiotics in less than 5 h. The device could assist physicians and veterinarians to make more targeted and rapid prescriptions for antibiotic infections.
Skin-nerve crosstalk is a major element of skin physiological pathology. Here the authors report a 3D innervated epidermal keratinocyte layer as a sensory neuron-epidermal keratinocyte coculture model on a microfluidic chip using the slope-based air-liquid interfacing culture and spatial compartmentalization.
Normal and abnormal pregnancy is challenging to study and involves complex interactions between maternal and fetal cells. Here the authors present an implantation-on-a-chip device capable of modeling trophoblast invasion, a process critical to the establishment of pregnancy.
Here the authors develop perfusable inner blood-retinal barrier-specific microvascular networks with human primary retinal microvascular cells. They show that chronic diabetic stimulation leads to the generation of early hallmarks of diabetic retinopathy, including pericyte and capillary dropout, ghost vessels, and inflammation.
A unique 3D-printed device made of sustainable materials was developed to produce 3D spheroids from primary cells and perform drug screening assays in a biomimetic environment.
Acute exposure to radiation can lead to acute pneumonitis, fibrosis or death. Here the authors develop an alveolus-on chip model to study the molecular characteristics of radiation induced lung injury, better understand radiation induced lung disease and facilitate drug screening.
A model system for studying non-alcoholic fatty liver disease is created by co-culturing human gut and liver cell lines in a closed circulation loop using microfluidics.
A biomimetic inducible model of pulmonary arterial hypertension (PAH) is presented, combining natural and induced BMPR2 dysfunction with hypoxia in lung endothelial cells and blood-derived PAH cells to induce smooth muscle activation & proliferation.
Understanding host responses to Herpes simplex virus (HSV) in humans is challenging. Here the authors report a vascularised 3D ‘skin-on-chip’ that mimics human skin architecture and is competent to immune-cell and drug perfusion; they use this to model HSV infection.