Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-c47g7 Total loading time: 0 Render date: 2024-04-25T06:20:54.544Z Has data issue: false hasContentIssue false

28 - Transplantation of Schwann cells and olfactory ensheathing cells to promote regeneration in the CNS

from Section B3 - Promotion of regeneration in the injured nervous system

Published online by Cambridge University Press:  05 March 2012

Mary Bartlett Bunge
Affiliation:
The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, FL, USA
Patrick M. Wood
Affiliation:
The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, FL, USA
Michael Selzer
Affiliation:
University of Pennsylvania
Stephanie Clarke
Affiliation:
Université de Lausanne, Switzerland
Leonardo Cohen
Affiliation:
National Institute of Mental Health, Bethesda, Maryland
Pamela Duncan
Affiliation:
University of Florida
Fred Gage
Affiliation:
Salk Institute for Biological Studies, San Diego
Get access

Summary

The goal of this chapter is to provide an overview of the efficacy of Schwann cell (SC) and olfactory ensheathing cell (OEC) transplantation to repair the central nervous system (CNS). A transplanted bridge of cells to span the site of injury is a promising strategy to provide a permissive scaffold for axonal growth (reviewed in Bunge, 2001; Geller and Fawcett, 2002). Both cell types have been shown to be effective; both cell types offer advantages. SCs may be easily extricated from peripheral nerve and placed into culture to generate far larger numbers than OECs; they effectively myelinate regenerated fibers or remyelinate denuded axons in vivo. Because they do not invade astrocyte territory, they are not as migratory as OECs and additional strategies are needed to lure the regenerated fibers from the SC implant, unlike OECs. OECs are less accessible and are not yet available in large numbers, but they have been demonstrated to be reparative, including improving functional outcome, in certain lesion paradigms. They normally occupy an area of the mammalian CNS that undergoes continuous nerve fiber growth throughout adult life. Repair of the spinal cord receives most attention in this chapter because the constraints on page length and reference number preclude a more inclusive review. SC and OEC transplantation have been compared earlier (Plant et al., 2001b).

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×