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Sökning: onr:"swepub:oai:DiVA.org:liu-158326" > Peripheral Nerve Re...

Peripheral Nerve Regeneration Is Independent From Schwann Cell p75(NTR) Expression

Goncalves, Nadia P. (författare)
Aarhus Univ, Denmark; Aarhus Univ Hosp, Denmark
Mohseni, Simin (författare)
Linköpings universitet,Avdelning för neurobiologi,Medicinska fakulteten
El Soury, Marwa (författare)
Univ Turin, Italy
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Ulrichsen, Maj (författare)
Aarhus Univ, Denmark
Richner, Mette (författare)
Aarhus Univ, Denmark
Xiao, Junhua (författare)
Univ Melbourne, Australia
Wood, Rhiannon J. (författare)
Univ Melbourne, Australia
Andersen, Olav M. (författare)
Aarhus Univ, Denmark
Coulson, Elizabeth J. (författare)
Univ Queensland, Australia
Raimondo, Stefania (författare)
Univ Melbourne, Australia
Murray, Simon S. (författare)
Univ Melbourne, Australia
Vaegter, Christian B. (författare)
Aarhus Univ, Denmark; Aarhus Univ Hosp, Denmark
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 (creator_code:org_t)
2019-05-29
2019
Engelska.
Ingår i: Frontiers in Cellular Neuroscience. - : FRONTIERS MEDIA SA. - 1662-5102. ; 13
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Schwann cell reprogramming and differentiation are crucial prerequisites for neuronal regeneration and re-myelination to occur following injury to peripheral nerves. The neurotrophin receptor p75(NTR) has been identified as a positive modulator for Schwann cell myelination during development and implicated in promoting nerve regeneration after injury. However, most studies base this conclusion on results obtained from complete p75(NTR) knockout mouse models and cannot dissect the specific role of p75(NTR) expressed by Schwann cells. In this present study, a conditional knockout model selectively deleting p75(NTR) expression in Schwann cells was generated, where p75(NTR) expression is replaced with that of an mCherry reporter. Silencing of Schwann cell p75(NTR) expression was confirmed in the sciatic nerve in vivo and in vitro, without altering axonal expression of p75(NTR). No difference in sciatic nerve myelination during development or following sciatic nerve crush injury was observed, as determined by quantification of both myelinated and unmyelinated nerve fiber densities, myelinated axonal diameter and myelin thickness. However, the absence of Schwann cell p75(NTR) reduced motor nerve conduction velocity after crush injury. Our data indicate that the absence of Schwann cell p75(NTR) expression in vivo is not critical for axonal regrowth or remyelination following sciatic nerve crush injury, but does play a key role in functional recovery. Overall, this represents the first step in redefining the role of p75(NTR) in the peripheral nervous system, suggesting that the Schwann cell-axon unit functions as a syncytium, with the previous published involvement of p75(NTR) in remyelination most likely depending on axonal/neuronal p75(NTR) and/or mutual glial-axonal interactions.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Nyckelord

Schwann cells; p75(NTR); myelination; regeneration; nerve injury

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