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Krishnamurthy, V. T.

Publications and source records attributed to Krishnamurthy, V. T..

2 recordsLinked to original sources

Microgels enable iPSCs to assemble, expand, and differentiate into organoids -- from sizable to high throughput

Organoid research holds tremendous potential for personalized medicine and drug development. However, current limitations include reproducibility issues largely due to the use of biologically derived materials, which are prone to batch-to-batch variations. Here, we report a new technology for human induced pluripotent stem cell (iPSC)-based organoid production with iPSC expansion and differentiation in the same construct in a reproducible and scalable manner, compatible with high-throughput automation. Chemically defined poly(ethylene glycol) (PEG)-based microgels are produced via parallelized step-emulsification microfluidics, enabling scalable production. This approach leverages the self-organization of iPSCs with microgels to build three-dimensional constructs, driven by robust cell-material interactions achieved through vitronectin-coated PEG microgels. This technology allows the iPSCs to expand and retain their pluripotency, after which they can be differentiated into the three germ layers, providing a suitable platform for organoid differentiation. This was further extended by differentiation into cardiac organoids and retinal photoreceptors to demonstrate two exemplary tissues.

bioengineering↗

Photodegradable Hydrogels for On-Demand Modeling of Age-Related Spatiotemporal ECM Deformation

The extracellular matrix (ECM) plays a crucial role in regulating tissue behavior through a dynamic interplay of spatial and temporal cues. Dynamic materials capable of modulating these cues at relevant scales are essential for tackling current challenges in tissue engineering and addressing fundamental biological questions. In vision research, there is a notable lack of suitable in vitro systems to study ECM dynamics. To help fill this gap, we developed an easy-to-use, photosensitive poly(ethylene glycol)-based hydrogel that can deform on demand to simulate ECM bulging, known as drusen, associated with the aging of the outer retina. Our findings demonstrate that variations in the size of these artificial drusen during culture impact morphometric parameters of the retinal pigment epithelium, offering new insights into its mechanical resilience to different drusen sizes. Notably, drusen formation in our system does not significantly affect the cellular actin cytoskeleton or polarity, which are often disrupted in conventional acute substrate deformation models, allowing the study of early aging before detectable pathology. In summary, we present a light-tunable hydrogel platform that enables precise spatial mimicry of ECM topographical changes, offering a promising tool for investigating the mechanobiological aspects of dynamic cell-matrix interactions.

bioengineering↗