1999
DOI: 10.1016/s0361-9230(99)00035-0
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Glial cells in degenerating and regenerating optic nerve of the adult rat

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Cited by 20 publications
(11 citation statements)
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“…In principle, Schwann cells are crucial for PNS regeneration, even when artificial nerve conduits are used; Schwann cells migrate out from both the proximal and distal nerve ends into the gap space and provide a cellular foothold to support axonal regrowth and to guide regenerating axons to the distal nerve segment where activated Schwann cells form cordons [17]. Axons successfully elongate over a long distance, mostly while in contact with cellular footholds such as Schwann cells, but long regrowth does not occur when only extracellular matrices are provided [18][19][20]. Therefore, when the gap is long, the limited Schwann cell migration results in limited regeneration efficiency.…”
Section: Introductionmentioning
confidence: 99%
“…In principle, Schwann cells are crucial for PNS regeneration, even when artificial nerve conduits are used; Schwann cells migrate out from both the proximal and distal nerve ends into the gap space and provide a cellular foothold to support axonal regrowth and to guide regenerating axons to the distal nerve segment where activated Schwann cells form cordons [17]. Axons successfully elongate over a long distance, mostly while in contact with cellular footholds such as Schwann cells, but long regrowth does not occur when only extracellular matrices are provided [18][19][20]. Therefore, when the gap is long, the limited Schwann cell migration results in limited regeneration efficiency.…”
Section: Introductionmentioning
confidence: 99%
“…However, it is also clear that astrocytes are not always nonpermissive for axonal growth. In fact, there appear to be differences in the ability of astrocytes to support axonal growth, depending on the degree of differentiation of the cells (Baehr and Bunge, 1989;Hatten et al, 1991;Lucius et al, 1996); on whether the astrocytes have formed a two-or three-dimensional substratum for the growing axons (Fawcett et al, 1989); on the part of the CNS that is injured (Alonso and Privat, 1993a,b;Chauvet et al, 1998;Prieto et al, 2000); and on the presence or absence of macrophages (David et al, 1990), Schwann cells Dezawa et al, 1999) or OECs (Li et al, 1997(Li et al, , 1998.…”
Section: Are Oecs a Clinically Relevant Alternative To Schwann Cells?mentioning
confidence: 99%
“…We hypothesize that OECs, by virtue of their ability to integrate and migrate within the CNS microenvironment, effectively modify the response of astrocytes and microglia to create a more supportive environment for the regeneration of axons. The microglial cell response to tissue injury has been shown to be modified by the presence of Schwann cells (Zeev-Brann et al, 1998;Dezawa et al, 1999), and some studies have found that CNS axons can regenerate through areas of tissue injury containing microglial cells/ macrophages (Prewitt et al, 1997;Rabchevsky and Streit, 1997;LazarovSpiegler et al, 1998;Stichel et al, 1999).…”
Section: Are Oecs a Clinically Relevant Alternative To Schwann Cells?mentioning
confidence: 99%
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