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Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury.

Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury. Research Abstract Details 

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  • Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury. Abstract Text:

    paul luPaul Lu,hong yangHong Yang,maya culbertsonMaya Culbertson,lori grahamLori Graham,a jane roskamsA Jane Roskams,mark h tuszynskiMark H Tuszynski,

    Olfactory ensheathing cells (OECs) have been reported to migrate long distances and to bridge lesion sites, guiding axonal regeneration after spinal cord injury (SCI). To understand mechanisms of OEC migration and axonal guidance, we injected lamina propria OECs 1 mm rostral and caudal to C4 SCI sites. One month later, OECs formed an apparent migrating cell tract continuously extending from the injection site through the lesion, physically bridging the lesion. Confocal immunolabeling demonstrated that, whereas this cell tract displaced host astrocytes, descending or ascending long tract axons did not preferentially extend into the cell tract and OECs failed to support bridging of corticospinal axons. Notably, the "bridging" tract of OECs formed within 1 h of cell injection, raising the possibility that cells passively spread from the pressure injection site rather than actively migrating. Control injections of bone marrow stromal cells (MSCs) or fibroblasts 1 mm from the lesion site also rapidly dispersed into the lesion cavity. Cell tracts extending into the lesion site were not seen when cells were injected either at low volumes, into spinal cord gray matter, or 3 d before or 9 d after SCI. OECs proliferated in injection sites, cell tracts, and lesion sites, indicating that OECs can also accumulate through cell proliferation. Thus, OECs do not appear to exhibit significant migratory properties when grafted to the spinal cord, exhibit no detectable difference in promoting axon growth into a SCI site compared with MSCs or fibroblasts, and do not support bridging of corticospinal axons beyond a dorsal column lesion.

    Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury. Publishing Authors By Initials

    p luP Lu,h yangH Yang,m culbertsonM Culbertson,l grahamL Graham,aj roskamsAJ Roskams,mh tuszynskiMH Tuszynski,

    For similar nervous system diseases: central nervous system diseases: spinal cord diseases: spinal cord injuries research abstracts see: nervous system diseases: central nervous system diseases: spinal cord diseases: spinal cord injuries research

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    Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: The Journal of neuroscience : the official journal

    VOLUME: 26

    Page Numbers: 11120-30

    Journal Abbreviation: J. Neurosci.

    ISSN: 1529-2401

    DAY: 25

    MONTH: Oct

    YEAR: 2006

    Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8102140

    Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury. Keywords Mesh Terms:

    KEYWORDS: Spinal Cord Injuries

    MESH TERMS: surgery

    Chemical & Substance for Abstract: Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury. Information

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    Grant and Affiliation Information for Olfactory ensheathing cells do not exhibit unique migratory or axonal growth-promoting properties after spinal cord injury.

    AFFILIATION: Department of Neuroscience, University of California at San Diego, La Jolla, California 92093, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NINDS

    GRANT: R01 NS09881

    ACRONYM: NS

    MEDLINETA: J Neurosci

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    Number Hits: 0

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