4.6 Review

Melatonin, tunneling nanotubes, mesenchymal cells, and tissue regeneration

Journal

NEURAL REGENERATION RESEARCH
Volume 18, Issue 4, Pages 760-762

Publisher

WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/1673-5374.353480

Keywords

brain ischemia; cell transplantation; melatonin; mesenchymal stem cell; mitochondria; mitochondrial transplantation; regenerative therapy; senescence; tunneling nanotubes

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This review discusses the potential utility of melatonin in preserving the survival and function of mesenchymal stem cells after transplantation. Melatonin regulates critical cell functions including apoptosis, endoplasmic reticulum stress, and autophagy. Recent findings also suggest that melatonin promotes the formation of tunneling nanotubes and the transfer of mitochondria between cells. By improving mitochondrial functionality and facilitating their transfer through tunneling nanotubes, melatonin has the potential to enhance mesenchymal stem cell-based therapy.
Mesenchymal stem cells are multipotent stem cells that reside in many human tissues and organs. Mesenchymal stem cells are widely used in experimental and clinical regenerative medicine due to their capability to transdifferentiate into various lineages. However, when transplanted, they lose part of their multipotency and immunomodulatory properties, and most of them die after injection into the damaged tissue. In this review, we discuss the potential utility of melatonin in preserving mesenchymal stem cells' survival and function after transplantation. Melatonin is a pleiotropic molecule regulating critical cell functions including apoptosis, endoplasmic reticulum stress, and autophagy. Melatonin is also synthesized in the mitochondria where it reduces oxidative stress, the opening of the mitochondrial permeability transition pore and the downstream caspase activation, activates uncoupling proteins, and curtails the proinflammatory response. In addition, recent findings showed that melatonin also promotes the formation of tunneling nanotubes and the transfer of mitochondria between cells through the connecting tubules. As mitochondrial dysfunction is a primary cause of mesenchymal stem cells death and senescence and a critical issue for survival after transplantation, we propose that melatonin by favoring mitochondria functionality and their transfer through tunneling nanotubes from healthy to suffering cells could improve mesenchymal stem cell-based therapy in a large number of diseases for which basic and clinical trials are underway.

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