Publications by authors named "Kirill Sukhinich"

Background: Cell therapy using neural progenitor cells (NPCs) is a promising approach for ischemic stroke treatment according to the results of multiple preclinical studies in animal stroke models. In the vast majority of conducted animal studies, the therapeutic efficacy of NPCs was estimated after intracerebral transplantation, while the information of the effectiveness of systemic administration is limited. Nowadays, several clinical trials aimed to estimate the safety and efficacy of NPCs transplantation in stroke patients were also conducted.

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Article Synopsis
  • Systemic transplantation of mesenchymal stem cells (MSCs) shows potential for treating ischemia-related issues like stroke, though the exact benefits are still unclear.
  • * Researchers developed an MRI method to track how MSCs spread in a live rat brain after a stroke, noting their accumulation in brain vessels shortly after being administered.
  • * Despite the low number of MSCs present in the brain and their short retention time, the treatment led to lasting improvements in neurological function without significantly reducing stroke damage compared to control rats.*
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Restoring the anatomical and functional characteristics of the cornea using various biomaterials is especially relevant in the context of a global shortage of donor tissue. Such biomaterials must be biocompatible, strong, and transparent. Here, we report a Viscoll collagen membrane with mechanical and optical properties suitable for replacing damaged stromal tissue.

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Article Synopsis
  • - Researchers explored how well mesenchymal stem cells (MSCs) can be delivered to brain tissue through intra-arterial (IA) transplantation, particularly for treating neurological disorders like stroke.
  • - They studied the relationship between brain blood flow (perfusion) and MSC distribution in both healthy rats and rats with stroke, using advanced MR imaging techniques.
  • - Results showed that brain perfusion partially influences where the MSCs end up after transplantation, but other unknown factors also play a significant role, indicating that more research is needed.
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Animal model studies and first clinical trials have demonstrated the safety and efficacy of the mesenchymal stem cells' (MSCs) transplantation in stroke. Intra-arterial (IA) administration looks especially promising, since it provides targeted cell delivery to the ischemic brain, is highly effective, and can be safe as long as the infusion is conducted appropriately. However, wider clinical application of the IA MSCs transplantation will only be possible after a better understanding of the mechanism of their therapeutic action is achieved.

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Article Synopsis
  • - Cell therapy, particularly using directly reprogrammed neural precursor cells (drNPC), shows promise for reducing brain damage and improving recovery after a stroke, as tested in a rat model.
  • - The study involved infusing drNPC into the bloodstream of rats 24 hours post-stroke, allowing tracking of these cells via MRI; results indicated that drNPC were present near and within the infarct zone more quickly than the control group of placenta-derived mesenchymal stem cells (pMSC).
  • - Both drNPC and pMSC improved neurological function and reduced stroke effects, but they acted differently in terms of infarct volume and animal survival, hinting at unique therapeutic mechanisms at play, particularly for drNPC.
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Cell therapy of neurological diseases is gaining momentum. Various types of stem/progenitor cells and their derivatives have shown positive therapeutic results in animal models of neurological disorders and in clinical trials. Each tested cell type proved to have its advantages and flaws and unique cellular and molecular mechanism of action, prompting the idea to test combined transplantation of two or more types of cells (combined cell therapy).

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Background: The regeneration of the peripheral nerves after injuries is still a challenging fundamental and clinical problem. The cell therapy and nerve guide conduit construction are promising modern approaches. Nowadays, different sources of cells for transplantation are available.

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Neural crest stem cells that located in the postnatal hair follicle (HF-NCSC) are considered a promising tool for treatment of nervous system diseases and injuries. It is well known that HF-NCSC can be used in the spinal cord and sciatic nerve reparation but their ability to restore brain structures is poorly studied. In this article we are investigating the interaction between HF-NCSC and a nerve tissue (embryonic and adult).

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In vivo tracking of transplanted mesenchymal stem cells (MSCs) migration and homing is vital for understanding the mechanisms of beneficial effects of MSCs transplantation in animal models of diseases and in clinical trials. Transplanted cells can be labeled with superparamagnetic iron oxide (SPIO) particles and visualized in vivo using a number of iron sensitive MRI techniques. However, the applicability of those techniques for SPIO-labeled MSCs tracking in live brain has not been sufficiently investigated.

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