Life sciences · Journal article
Cell Communication and Signaling · October 3, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Journal article.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Abstract Among their diverse functions, platelets enable intercellular communication through the release of their contents, including functional mitochondria. Given their high circulatory abundance, platelets represent a readily accessible source of these organelles. Consequently, platelet-derived mitochondria (PDM) are increasingly recognized as active mediators of intercellular signaling and metabolic remodeling. This review synthesizes current knowledge regarding the mechanisms underlying PDM release, intercellular transfer, and uptake by diverse recipient cells. We further highlight the emerging roles of PDM in cancer progression, immune regulation, and tissue regeneration. While growing evidence underscores the therapeutic potential of PDM, particularly in mitochondria transplantation, critical challenges remain, including the standardization of isolation protocols, assessment of long-term efficacy, and potential off-target effects. Finally, we summarize recent advances and outline research priorities to facilitate the safe and effective clinical translation of PDM-based therapies.