Intraventricular hemorrhage (IVH)—or bleeding in the brain—is a devastating condition common to premature babies, especially those born more than 10 weeks early. Injuries to the brain induced by severe IVH and the ensuing pressure caused by fluid buildup (known as post-hemorrhagic hydrocephalus, or PHH) can result in seizures, cerebral palsy, developmental retardation and an increased mortality rate. There is currently no effective treatment for IVH, but a study released today in STEM CELLS Translational Medicine provides information that might change that.
The study, by researchers at Sungkyunkwan University in Seoul, shows how extracellular vesicles (EVs) derived from mesenchymal stem cells (MSCs) can ease IVH-induced brain injuries. It also reveals that a protein-coding gene called brain-derived neurotrophic factor (BDNF), secreted by MSCs and transferred through EVs, is likely the key factor behind these beneficial effects.
MSCs are multipotent adult stem cells present in umbilical cord, bone marrow, fat, dental and other body tissues. Their ability to secrete biologically active molecules that exert beneficial effects on injured tissues makes them a promising target in regenerative medicine. Recent studies and clinical trials have shown that MSC-derived EVs (membranes that contain proteins, lipids and RNAs) can safely recreate the therapeutic efficacy of parent MSCs in various neonatal disorders. Moreover, as these MSC-derived EVs are a cell-free therapy, they bypass many concerns associated with MSC transplantation, such as the potential to form tumors or cause pulmonary embolisms, or a chance of the cells being rejected.
“This all has led to the questions of whether MSC-derived EVs might serve as a surrogate for stem cell therapy in cases of severe IVH and, if so, whether the neuroprotection is related to protein transfer from EVs to the damaged host brain tissue,” said the current study’s corresponding author, Won Soon Park, M.D., Ph.D.
To find the answers, they applied either MSCs, MSC-derived EVs with or without BDNF knockdown, or fibroblast-derived EVs in vitro to rat neuronal cells that had first been exposed to thrombin to induce cell death. They repeated the process in vivo by injecting 4-day-old rats with 200 μL of blood to induce severe IVH, and then two days later treating them with a transplantation of either MSCs or one of the EV groups. (A non-treated group of newborn rats was used as a control.) The results were assessed via MRIs and functional behavioral tests.
“We learned that the MSCs and MSC-derived EVs—but not the EVs derived from BDNF-knockdown MSCs or fibroblasts—significantly reduced both the thrombin-induced neuronal cell death in vitro and the severe IVH-induced brain injuries and inflammatory responses in vivo,” Dr. Park said. “As such, our data indicate that MSC-derived EVs are as effective as parental MSCs in attenuating severe IVH-induced brain injuries, and this neuroprotection is primarily mediated by BDNF transfer via EVs. We hope now to move on to establishing the optimal timing, route and dosage of the MSC-derived EVs.”
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