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The development of highly efficient antioxidant nanomaterials is crucial for protecting stem cells from oxidative stress, a major challenge in advancing stem cell therapy and tissue regeneration. While most existing materials focus on scavenging reactive oxygen species (ROS), the often-overlooked contribution of reactive nitrogen species (RNS) further amplifies oxidative damage, limiting therapeutic efficacy. Here, we report a manganese-doped bimetallic metal-organic framework (MOF), Dex@(Mn, Zn)EZIF-8, with a hollow architecture designed for precise ROS/RNS scavenging and osteogenic regulation. This MOF is synthesized a one-pot method, followed by tannic acid-assisted etching and Dex loading. The incorporation of Mn, a transition metal with tunable valence states, significantly enhances catalase-like activity for ROS degradation, while tannic acid etching introduces additional sites for RNS neutralization. By mitigating oxidative stress, Dex@(Mn, Zn)EZIF-8 preserves the viability and essential functions of bone mesenchymal stem cells, including adhesion, proliferation, and migration, while also promoting osteogenic differentiation. Furthermore, the sustained release of Dex amplifies osteogenesis, as evidenced by the upregulated expression of key markers such as alkaline phosphatase, osteopontin, and osteocalcin. This multifunctional biocatalyst effectively integrates precision oxidative stress regulation with osteogenic promotion, offering a powerful strategy for stem cell protection and regenerative medicine, particularly in oxidative microenvironments.
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http://dx.doi.org/10.1039/d5nr00890e | DOI Listing |
JCI Insight
September 2025
Division of Nephrology, Boston University Chobanian & Avedisian School of Medicine, Boston, United States of America.
Background: Active vitamin D metabolites, including 25-hydroxyvitamin D (25D) and 1,25-dihydroxyvitamin D (1,25D), have potent immunomodulatory effects that attenuate acute kidney injury (AKI) in animal models.
Methods: We conducted a phase 2, randomized, double-blind, multiple-dose, 3-arm clinical trial comparing oral calcifediol (25D), calcitriol (1,25D), and placebo among 150 critically ill adult patients at high-risk of moderate-to-severe AKI. The primary endpoint was a hierarchical composite of death, kidney replacement therapy (KRT), and kidney injury (baseline-adjusted mean change in serum creatinine), each assessed within 7 days following enrollment using a rank-based procedure.
J Clin Invest
September 2025
Department of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, United Kingdom.
Understanding the genetic causes of diseases affecting pancreatic β cells and neurons can give insights into pathways essential for both cell types. Microcephaly, epilepsy and diabetes syndrome (MEDS) is a congenital disorder with two known aetiological genes, IER3IP1 and YIPF5. Both genes encode proteins involved in endoplasmic reticulum (ER) to Golgi trafficking.
View Article and Find Full Text PDFRNA Biol
September 2025
Department of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, Republic of Korea.
Neural stem cells (NSCs) are multipotent stem cells with self-renewal capacity, able to differentiate into all neural lineages of the central nervous system, including neurons, oligodendrocytes, and astrocytes; thus, their proliferation and differentiation are essential for embryonic neurodevelopment and adult brain homoeostasis. Dysregulation in these processes is implicated in neurological disorders, highlighting the need to elucidate how NSCs proliferate and differentiate to clarify the mechanisms of neurogenesis and uncover potential therapeutic targets. MicroRNAs (miRNAs) are small, post-transcriptional regulators of gene expression involved in many aspects of nervous system development and function.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
School of Medicine, Chongqing University, Chongqing 400044, China.
Engineering functional exosomes represents a cutting-edge approach in biomedicine, holding the promise to transform targeted therapy. However, challenges such as achieving consistent modification and scalability have limited their wider adoption. Herein, we introduce a universal and effective strategy for engineering multifunctional exosomes through cell fusion.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202.
Retinal ganglion cells (RGCs) are highly compartmentalized neurons whose long axons serve as the sole connection between the eye and the brain. In both injury and disease, RGC degeneration occurs in a similarly compartmentalized manner, with distinct molecular and cellular responses in the axonal and somatodendritic regions. The goal of this study was to establish a microfluidic-based platform to investigate RGC compartmentalization in both health and disease states.
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