Back to Search Start Over

Lithium modulates miR‐1906 levels of mesenchymal stem cell‐derived extracellular vesicles contributing to poststroke neuroprotection by toll‐like receptor 4 regulation

Authors :
Dirk M. Hermann
Lisa Janssen
Xuan Zheng
Vivek Venkataramani
Thorsten R. Doeppner
Bert Bosche
Matteo Haupt
Katharina Hein
Simone Lieschke
Yaoyun Kuang
Mathias Bähr
Ertugrul Kilic
Fengyan Jin
Source :
Stem Cells Translational Medicine, Vol 10, Iss 3, Pp 357-373 (2021), Stem Cells Translational Medicine
Publication Year :
2021
Publisher :
Wiley, 2021.

Abstract

Lithium is neuroprotective in preclinical stroke models. In addition to that, poststroke neuroregeneration is stimulated upon transplantation of mesenchymal stem cells (MSCs). Preconditioning of MSCs with lithium further enhances the neuroregenerative potential of MSCs, which act by secreting extracellular vesicles (EVs). The present work analyzed whether MSC preconditioning with lithium modifies EV secretion patterns, enhancing the therapeutic potential of such derived EVs (Li‐EVs) in comparison with EVs enriched from native MSCs. Indeed, Li‐EVs significantly enhanced the resistance of cultured astrocytes, microglia, and neurons against hypoxic injury when compared with controls and to native EV‐treated cells. Using a stroke mouse model, intravenous delivery of Li‐EVs increased neurological recovery and neuroregeneration for as long as 3 months in comparison with controls and EV‐treated mice, albeit the latter also showed significantly better behavioral test performance compared with controls. Preconditioning of MSCs with lithium also changed the secretion patterns for such EVs, modifying the contents of various miRNAs within these vesicles. As such, Li‐EVs displayed significantly increased levels of miR‐1906, which has been shown to be a new regulator of toll‐like receptor 4 (TLR4) signaling. Li‐EVs reduced posthypoxic and postischemic TLR4 abundance, resulting in an inhibition of the nuclear factor kappa‐light‐chain‐enhancer of activated B cells (NF‐κB) signaling pathway, decreased proteasomal activity, and declined both inducible NO synthase and cyclooxygenase‐2 expression, all of which culminated in reduced levels of poststroke cerebral inflammation. Conclusively, the present study demonstrates, for the first time, an enhanced therapeutic potential of Li‐EVs compared with native EVs, interfering with a novel signaling pathway that yields both acute neuroprotection and enhanced neurological recovery.<br />Lithium‐treated extracellular vesicles (Li‐EVs) induce neuroprotection, neuroregeneration, and neurological recovery under in vitro and in vivo stroke conditions. Increased concentrations of intravesicular miR‐1906 due to lithium treatment reduce toll‐like receptor 4 expression patterns. The latter results in reduction of NF‐κB activation and reduced proteasomal activity followed by decreased levels of pro‐inflammatory mediators within the ischemic brain. Likewise, Li‐EVs reverse the poststroke peripheral immunosuppression.

Details

Language :
English
ISSN :
21576564 and 21576580
Volume :
10
Issue :
3
Database :
OpenAIRE
Journal :
Stem Cells Translational Medicine
Accession number :
edsair.doi.dedup.....a816a5d44ee67ae6d114cf523dc723b3