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We are analyzing https://link.springer.com/article/10.1007/s11064-007-9426-6.

Title:
Umbilical Cord Blood Stem Cell Mediated Downregulation of Fas Improves Functional Recovery of Rats after Spinal Cord Injury | Neurochemical Research
Description:
Human umbilical cord blood stem cells (hUCB), due to their primitive nature and ability to develop into nonhematopoietic cells of various tissue lineages, represent a potentially useful source for cell-based therapies after spinal cord injury (SCI). To evaluate their therapeutic potential, hUCB were stereotactically transplanted into the injury epicenter, one week after SCI in rats. Our results show the presence of a substantial number of surviving hUCB in the injured spinal cord up to five weeks after transplantation. Three weeks after SCI, apoptotic cells were found especially in the dorsal white matter and gray matter, which are positive for both neuron and oligodendrocyte markers. Expression of Fas on both neurons and oligodendrocytes was efficiently downregulated by hUCB. This ultimately resulted in downregulation of caspase-3 extrinsic pathway proteins involving increased expression of FLIP, XIAP and inhibition of PARP cleavage. In hUCB-treated rats, the PI3K/Akt pathway was also involved in antiapoptotic actions. Further, structural integrity of the cytoskeletal proteins ฮฑ-tubulin, MAP2A&2B and NF-200 has been preserved in hUCB treatments. The behavioral scores of hind limbs of hUCB-treated rats improved significantly than those of the injured group, showing functional recovery. Taken together, our results indicate that hUCB-mediated downregulation of Fas and caspases leads to functional recovery of hind limbs of rats after SCI.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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  • Education
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What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {๐Ÿ“ˆ}

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๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


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How Does Link.springer.com Make Money? {๐Ÿ’ธ}

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Keywords {๐Ÿ”}

cord, spinal, article, google, scholar, pubmed, cas, injury, cells, stem, apoptosis, rats, recovery, umbilical, cell, rat, fas, functional, neurosci, death, neurol, blood, human, caspase, springer, traumatic, exp, sci, factor, growth, res, function, research, hucb, brain, protein, peoria, privacy, cookies, content, improves, apoptotic, expression, access, degeneration, usa, publish, search, downregulation, jasti,

Topics {โœ’๏ธ}

month download article/chapter brain-derived neutrophic factor liang liย &ย jasti cytoskeletal proteins ฮฑ-tubulin calpain-dependent neurofilament breakdown hucb-mediated downregulation liang li spinal cord injury improves functional recovery cancer biology improves neurological function showing functional recovery fas-mediated apoptosis rat spinal cord apoptotic cell death injured spinal cord neuronal cell death spinal cord contusion spinal cord transplantation cell-based therapies cell therapy approaches spinal cord injuries spinal cord ischemia full article pdf apoptotic cells author information authors fas signaling mechanisms nonhematopoietic cells promotes oligodendroglial survival enhances axonal survival functional recovery privacy choices/manage cookies caspase-3 apoptotic cascade severe contusion injury pi3k/akt pathway open field testing article dasari spinal cord 43 spinal cord 36 related subjects x-linked inhibitor axotomy-induced death author correspondence map2a&2b dorsal white matter check access instant access nottingham sa fas antigen induction locomotor recovery

Schema {๐Ÿ—บ๏ธ}

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         headline:Umbilical Cord Blood Stem Cell Mediated Downregulation of Fas Improves Functional Recovery of Rats after Spinal Cord Injury
         description:Human umbilical cord blood stem cells (hUCB), due to their primitive nature and ability to develop into nonhematopoietic cells of various tissue lineages, represent a potentially useful source for cell-based therapies after spinal cord injury (SCI). To evaluate their therapeutic potential, hUCB were stereotactically transplanted into the injury epicenter, one week after SCI in rats. Our results show the presence of a substantial number of surviving hUCB in the injured spinal cord up to five weeks after transplantation. Three weeks after SCI, apoptotic cells were found especially in the dorsal white matter and gray matter, which are positive for both neuron and oligodendrocyte markers. Expression of Fas on both neurons and oligodendrocytes was efficiently downregulated by hUCB. This ultimately resulted in downregulation of caspase-3 extrinsic pathway proteins involving increased expression of FLIP, XIAP and inhibition of PARP cleavage. In hUCB-treated rats, the PI3K/Akt pathway was also involved in antiapoptotic actions. Further, structural integrity of the cytoskeletal proteins ฮฑ-tubulin, MAP2A&2B and NF-200 has been preserved in hUCB treatments. The behavioral scores of hind limbs of hUCB-treated rats improved significantly than those of the injured group, showing functional recovery. Taken together, our results indicate that hUCB-mediated downregulation of Fas and caspases leads to functional recovery of hind limbs of rats after SCI.
         datePublished:2007-08-17T00:00:00Z
         dateModified:2007-08-17T00:00:00Z
         pageStart:134
         pageEnd:149
         sameAs:https://doi.org/10.1007/s11064-007-9426-6
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            Umbilical cord blood stem cells
            Apoptosis
            Fas
            Caspase-3
            Spinal cord Injury
            Functional recovery
            Neurosciences
            Neurochemistry
            Biochemistry
            general
            Cell Biology
            Neurology
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      headline:Umbilical Cord Blood Stem Cell Mediated Downregulation of Fas Improves Functional Recovery of Rats after Spinal Cord Injury
      description:Human umbilical cord blood stem cells (hUCB), due to their primitive nature and ability to develop into nonhematopoietic cells of various tissue lineages, represent a potentially useful source for cell-based therapies after spinal cord injury (SCI). To evaluate their therapeutic potential, hUCB were stereotactically transplanted into the injury epicenter, one week after SCI in rats. Our results show the presence of a substantial number of surviving hUCB in the injured spinal cord up to five weeks after transplantation. Three weeks after SCI, apoptotic cells were found especially in the dorsal white matter and gray matter, which are positive for both neuron and oligodendrocyte markers. Expression of Fas on both neurons and oligodendrocytes was efficiently downregulated by hUCB. This ultimately resulted in downregulation of caspase-3 extrinsic pathway proteins involving increased expression of FLIP, XIAP and inhibition of PARP cleavage. In hUCB-treated rats, the PI3K/Akt pathway was also involved in antiapoptotic actions. Further, structural integrity of the cytoskeletal proteins ฮฑ-tubulin, MAP2A&2B and NF-200 has been preserved in hUCB treatments. The behavioral scores of hind limbs of hUCB-treated rats improved significantly than those of the injured group, showing functional recovery. Taken together, our results indicate that hUCB-mediated downregulation of Fas and caspases leads to functional recovery of hind limbs of rats after SCI.
      datePublished:2007-08-17T00:00:00Z
      dateModified:2007-08-17T00:00:00Z
      pageStart:134
      pageEnd:149
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         Umbilical cord blood stem cells
         Apoptosis
         Fas
         Caspase-3
         Spinal cord Injury
         Functional recovery
         Neurosciences
         Neurochemistry
         Biochemistry
         general
         Cell Biology
         Neurology
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                     name:Department of Neurosurgery, University of Illinois College of Medicine at Peoria, Peoria, USA
                     type:PostalAddress
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                  name:University of Illinois College of Medicine
                  address:
                     name:Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria, USA
                     type:PostalAddress
                  type:Organization
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            affiliation:
                  name:University of Illinois College of Medicine at Peoria
                  address:
                     name:Department of Pathology, University of Illinois College of Medicine at Peoria, Peoria, USA
                     type:PostalAddress
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            name:Jasti S. Rao
            affiliation:
                  name:University of Illinois College of Medicine
                  address:
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                  name:University of Illinois College of Medicine at Peoria
                  address:
                     name:Department of Neurosurgery, University of Illinois College of Medicine at Peoria, Peoria, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Dzung H. Dinh
            affiliation:
                  name:University of Illinois College of Medicine at Peoria
                  address:
                     name:Department of Neurosurgery, University of Illinois College of Medicine at Peoria, Peoria, USA
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               type:PostalAddress
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      name:Jasti S. Rao
      affiliation:
            name:University of Illinois College of Medicine
            address:
               name:Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria, USA
               type:PostalAddress
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            type:Organization
      name:Dzung H. Dinh
      affiliation:
            name:University of Illinois College of Medicine at Peoria
            address:
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      name:Department of Pathology, University of Illinois College of Medicine at Peoria, Peoria, USA
      name:Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria, USA
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