Researchers at Texas A&M used microscopic molybdenum disulfide "nanoflowers" to stimulate stem cells to produce about twice the normal number of mitochondria and donate them to aging or injured cells. Reported in Proceedings of the National Academy of Sciences, the experiments were conducted in cell cultures; rat studies are planned to assess safety and efficacy. Experts call the results promising but caution that long-term safety of molybdenum disulfide in humans remains unproven. If validated, the technique could inform treatments for neurodegenerative, muscular and metabolic diseases.
Researchers 'Recharge' Cellular Powerhouses With Microscopic 'Nanoflowers' — A Potential Anti‑Aging Breakthrough
Aging shows up as wrinkles, thinning hair and slower thinking — but it also happens inside our cells as the tiny energy centers called mitochondria decline. Scientists at Texas A&M University report a laboratory method that re-energizes cells by prompting stem cells to produce and donate fresh mitochondria to aging or damaged cells. The work, published in Proceedings of the National Academy of Sciences (PNAS), could point toward new therapies for Alzheimer’s, muscular dystrophy, fatty liver disease and metabolic disorders such as diabetes.
How The Method Works
Gaharwar and colleagues treated cultured stem cells with microscopic, flower-shaped particles they call "nanoflowers." Made from the inorganic compound molybdenum disulfide, these particles are roughly 600–1,000 times smaller than the width of a human hair and enter stem cells through natural uptake pathways. Inside the stem cells the nanoflowers activate the pathways that generate mitochondria; treated stem cells produced about twice the normal number of mitochondria and were able to transfer those extra organelles to nearby aging or injured cells.
"The fact that you can increase the number of mitochondria per cell is huge," said Daria Mochly-Rosen, a Stanford professor who was not involved in the study.
Why This Matters
Mitochondria do more than make cellular energy: they participate in immune responses and help synthesize important molecules. Their loss or dysfunction is linked to multiple age-associated conditions and neurodegenerative and metabolic diseases. By boosting mitochondrial biogenesis in stem cells and exploiting mitochondria’s natural ability to move between cells, the Texas A&M team aims to use a patient’s own cells as a renewable source of healthy mitochondria.
From Petri Dish To Patients: The Road Ahead
Experiments to date were conducted in cell cultures. The researchers plan to start animal tests in rats in January or February to evaluate safety and efficacy in vivo. Any clinical use would require extensive preclinical testing and human trials. Existing drugs can raise mitochondrial numbers but often require repeated dosing; this cell-based approach seeks to create a durable, self-renewing source of mitochondria.
Cautions And Questions
Experts praised the advance but urged caution. Keshav K. Singh noted that long-term safety data for molybdenum disulfide in humans are lacking. Mochly-Rosen suggested an alternative possibility — direct injection of nanoflowers into injured tissue — but emphasized that safety and duration of benefit must be established.
Potential Clinical Scenario
One envisioned pathway: clinicians remove a patient’s skin cells, reprogram them into stem cells, expose those cells to mitochondria-boosting nanoflowers in the lab, and then return the energized stem cells to the patient. Those cells would circulate, home to damaged tissue and donate healthy mitochondria, potentially improving neuronal communication or glucose handling in metabolic diseases.
The findings represent an intriguing step toward therapies that target cellular energy systems, but meaningful application in people will depend on the results of forthcoming animal studies and rigorous safety testing.
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