In Vivo Direct Reprogramming: Current Progress and Future Prospects from Mechanisms to Therapeutic Application
Abstract
Direct reprogramming, which converts somatic cells from one lineage to another without passing through a pluripotent state, represents a promising therapeutic strategy for regenerative medicine. Recent advancements in identifying reprogramming factors and understanding molecular barriers have enabled efficient generation of therapeutically relevant cells. Yet, the clinical application of in vitro-derived reprogrammed cells is hampered by the immature phenotype, hostile microenvironments, low engraftment, and poor survival after transplantation. In vivo direct reprogramming of tissue-resident cells within their native tissue microenvironment offers a compelling alternative to overcome these barriers. Harnessing biochemical and biophysical cues of the tissue microenvironment, this approach facilitates the acquisition of molecular and functional features resembling endogenous cells. This review summarizes the current understanding of in vivo direct reprogramming, covering mechanisms, key reprogramming factors, and delivery strategies, and explores therapeutic applications across organ systems. Finally, key challenges such as delivery efficiency, incomplete understanding of tissue cues, and limited mechanistic insights, along with emerging strategies, are discussed.
How strong is the evidence?
Evidence Hub reads this as a review, done in animal, not in people. Its evidence level is 5 of 5 (Very low · case / narrative / animal / in vitro / in silico). Case reports, narrative reviews, and animal, cell or computer-model studies give the weakest evidence for human health.
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