Bruno J. Manadas

The paper compares the neuroprotective effects of bone marrow MSCs and iPSC-derived MSCs secretomes in a Parkinson's disease model, finding that iMSCs secretome better preserves dopaminergic neurons and activates broader protective pathways.

This study compares host proteomic responses to four SFG Rickettsia species in endothelial cells, revealing distinct immune activation patterns linked to pathogenicity.

This study compares prolonged mild hypoxia and short severe hypoxia preconditioning of UC-MSCs for neonatal HIE treatment, finding that short severe hypoxia improves functional recovery and alters proteomic pathways related to neural repair.

This study shows that intranasal administration of hypoxia-preconditioned mesenchymal stem cells or their secretome improves recovery in neonatal HIE rats, even at low doses.

This study shows that physioxia-modulated UC-MSC secretome better preserves neuronal network and translation processes in an in vitro HIE model than traditional UC-MSCs.

This study shows that culturing mesenchymal stem cells under physiological stiffness and oxygen conditions increases secretion of redox and immunomodulatory proteins while reducing extracellular matrix proteins.

This paper shows that culturing MSCs on soft substrates or under low oxygen levels alters their proteome, promoting a more naive phenotype by affecting redox homeostasis, protein chaperones, and translational complexity.

This study shows that Huntington's Disease leads to increased release of mitochondrial components via extracellular vesicles due to mitochondrial and lysosomal dysfunction.