Precision medicine used to counteract oxidative stress in stroke animal model.
Researchers have known that transplanted human umbilical cord cells (HUCBCs) can have a restorative effect on the brain and brain function following a stroke. However, just how the cells exert their therapeutic effects has not been clear. Now, a research team from the University of South Florida using animal models of stroke has found that the HUCBCs are most beneficial in preventing neuron loss when the Akt signaling pathway is activated by secretions from the HUCBCs and that Akt activation subsequently impacts a specific gene involved in reducing inflammation. A reduction in inflammation can help neural cell survival following a stroke. The opensource study is published in Cell Transplantation.
The team state that stroke is the fourth leading cause of death and the leading cause of disability in the U.S. The goal of the study was to identify HUCB-induced neuronal genes associated with cell survival following a stroke and to discover just how soluble factors secreted by HUCBCs induce critical signaling pathways in neurons that enhance cell survival.
Four groups of laboratory rats modeled with stimulated stroke by oxygen or glucose deprivation were treated with or without HUCBCs. When the activation of the Akt pathway was confirmed in the HUCB-treated group, researchers found that the treated group had a 44 to 68 percent reduction in neuron loss when compared to the untreated groups.
The observations show that HUCB neuroprotection is dependent on the activation of the Akt signaling pathway that increases the transcription of the Peroxiredoxin-5 (Prdx5) gene. This finding suggests that HUCBC therapy could be a promising treatment for stroke and other forms of brain injury when gene expression is modified to promote neural protection.
While pathways other than Akt have been shown to be important in cell survival, Akt has been shown to be more important than others because it works to activate Prdx5, an antioxidant enzyme gene with the primary function of reducing hydrogen peroxide and inflammation. Prdx5 plays a significant role in the regulation of the transportation of certain molecules in apoptosis, or programmed cell death. Antioxidants have been shown to limit cell death and levels of Prdx5 have been found to be lower, and inflammation higher, in patients with more severe strokes.
This finding implies that in severe stroke Prdx5 is either degraded or its production is impaired. Prdx5 may be an important component of the antioxidant effect of HUCBCs and, therefore, a candidate for therapeutic targeting of oxidative stress in stroke.
The researchers concluded that HUCBCs rescued neural cells and prevented neuronal loss in rats modeled with stroke by increasing the transcription of genes related to survival and repair by inhibiting inflammation. It was the ramping up of Prdx5 through the Akt pathway that facilitated this effect. The neurosurvival action of secretants through Akt signaling not only ramped up transcription of Prdx5 and other survival-associated genes, but also inhibited genes that play a detrimental role in stroke injury.
The team surmise that this study provides hope of a treatment for stroke using HUCBCs, which are easily obtained, avoid ethical issues and have a minimal chance of rejection compared with other allogeneic stem cells, in order to rescue endogenous cells and restore function. The study also highlights the need for further understanding of the role of oxidative stress in the pathogenesis of stroke.
Source: University of South Florida
Akt signaling pathway, allogeneic stem cell, antioxidant, genetics, healthinnovations, human umbilical cord cells, immune response, immunology, neurogenetics, neuroinflammation, neuroinnovations, neuroprotection, opensource, oxidative stress, precision medicine, stem cell, stroke
Michelle Petersen View All
I am an award-winning science journalist and health industry veteran who has taught and worked in the field.
Featured by numerous prestigious brands and publishers, I specialize in clinical trial innovation–-expertise I gained while working in multiple positions within the private sector, the NHS, and Oxford University, where I taught undergraduates the spectrum of biological sciences integrating physics for over four years.
I recently secured tenure as a committee member for the Smart Works Charity, which helps women find employment in the UK.
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