TY - JOUR
T1 - Axotomy or compression is required for axonal sprouting following end-to-side neurorrhaphy
AU - Hayashi, Ayato
AU - Pannucci, Christopher
AU - Moradzadeh, Arash
AU - Kawamura, David
AU - Magill, Christina
AU - Hunter, Daniel A.
AU - Tong, Alice Y.
AU - Parsadanian, Alexander
AU - Mackinnon, Susan E.
AU - Myckatyn, Terence M.
N1 - Funding Information:
The authors are extremely grateful to Mr. S. Tuffaha for his assistance with Western analysis, and Ms. J. Luciano for maintaining, breeding, and genotyping the transgenic mouse lines. This work was funded by the National Institute of Health 5RO1NS051706-02 grant (S.E.M.). It was also funded by fellowship funding from the American College of Surgeons C. James Carrico Faculty Research Fellowship (T.M.M.) and the American Association of Plastic Surgeons John E. Hoopes Academic Scholarship (T.M.M.) The authors also recognize the Barnes-Jewish Foundation for confocal microscopy equipment support (S.E.M. and T.M.M.).
PY - 2008/6
Y1 - 2008/6
N2 - End-to-side (ETS) nerve repair remains an area of intense scrutiny for peripheral nerve surgeon-scientists. In this technique, the transected end of an injured nerve, representing the "recipient" is sutured to the side of an uninjured "donor" nerve. Some works suggest that the recipient limb is repopulated with regenerating collateral axonal sprouts from the donor nerve that go on to form functional synapses. Significant, unresolved questions include whether the donor nerve needs to be injured to facilitate regeneration, and whether a single donor neuron is capable of projecting additional axons capable of differentially innervating disparate targets. We serially imaged living transgenic mice (n = 66) expressing spectral variants of GFP in various neuronal subsets after undergoing previously described atraumatic, compressive, or epineurotomy forms of ETS repair (n = 22 per group). To evaluate the source, and target innervation of these regenerating axons, nerve morphometry and retrograde labeling were further supplemented by confocal microscopy as well as Western blot analysis. Either compression or epineurotomy with inevitable axotomy were required to facilitate axonal regeneration into the recipient limb. Progressively more injurious models were associated with improved recipient nerve reinnervation (epineurotomy: 184 ± 57.6 myelinated axons; compression: 78.9 ± 13.8; atraumatic: 0), increased Schwann cell proliferation (epineurotomy: 72.2% increase; compression: 39% increase) and cAMP response-element binding protein expression at the expense of a net deficit in donor axon counts distal to the repair. These differences were manifest by 150 days, at which point quantitative evidence for pruning was obtained. We conclude that ETS repair relies upon injury to the donor nerve.
AB - End-to-side (ETS) nerve repair remains an area of intense scrutiny for peripheral nerve surgeon-scientists. In this technique, the transected end of an injured nerve, representing the "recipient" is sutured to the side of an uninjured "donor" nerve. Some works suggest that the recipient limb is repopulated with regenerating collateral axonal sprouts from the donor nerve that go on to form functional synapses. Significant, unresolved questions include whether the donor nerve needs to be injured to facilitate regeneration, and whether a single donor neuron is capable of projecting additional axons capable of differentially innervating disparate targets. We serially imaged living transgenic mice (n = 66) expressing spectral variants of GFP in various neuronal subsets after undergoing previously described atraumatic, compressive, or epineurotomy forms of ETS repair (n = 22 per group). To evaluate the source, and target innervation of these regenerating axons, nerve morphometry and retrograde labeling were further supplemented by confocal microscopy as well as Western blot analysis. Either compression or epineurotomy with inevitable axotomy were required to facilitate axonal regeneration into the recipient limb. Progressively more injurious models were associated with improved recipient nerve reinnervation (epineurotomy: 184 ± 57.6 myelinated axons; compression: 78.9 ± 13.8; atraumatic: 0), increased Schwann cell proliferation (epineurotomy: 72.2% increase; compression: 39% increase) and cAMP response-element binding protein expression at the expense of a net deficit in donor axon counts distal to the repair. These differences were manifest by 150 days, at which point quantitative evidence for pruning was obtained. We conclude that ETS repair relies upon injury to the donor nerve.
KW - CREB
KW - End-to-side neurorrhaphy
KW - Epineurotomy
KW - Myelin associated glycoprotein
KW - Regeneration
KW - Transgenic
UR - http://www.scopus.com/inward/record.url?scp=43449111177&partnerID=8YFLogxK
U2 - 10.1016/j.expneurol.2008.02.031
DO - 10.1016/j.expneurol.2008.02.031
M3 - Article
C2 - 18433746
AN - SCOPUS:43449111177
SN - 0014-4886
VL - 211
SP - 539
EP - 550
JO - Experimental Neurology
JF - Experimental Neurology
IS - 2
ER -