Literature DB >> 1396177

The fate of Schwann cells transplanted in the brain during development.

A Baron-Van Evercooren1, E Clerin-Duhamel, P Lapie, A Gansmüller, F Lachapelle, M Gumpel.   

Abstract

Purified rat Schwann cells labeled with Hoechst 33342 fluorescent fluorochrome were transplanted into the brain of the newborn shiverer mouse. The grafted cells survived and were able to migrate through the host parenchyma. However, Schwann cell migration was restricted to the grafted hemisphere and to structures adjacent to the graft. With time, Hoechst labeled cells, present at the site of implantation or dispersed in the host parenchyma, decreased progressively in number. Instead, they concentrated along the blood vessels, meninges and ventricles. Despite the presence of Hoechst labeled Schwann cells in white matter tracks during the process of central myelination, Schwann cell myelination could not be evidenced by immunodetection of the peripheral myelin protein or by ultrastructural observation of the typical Schwann cell basement membrane surrounding peripheral myelin. A series of additional transplantations involving Schwann cells of mouse or rat origin, grafted either as cell suspensions or as nerve fragments, demonstrated that transplanted Schwann cells formed myelin around developing host axons only when included in a nerve fragment. Immunodetection of GFAP in astrocytes and type IV collagen in basement membranes as well as electron microscopy showed that reactive astrocytes invaded the grafted area after the first week of transplantation and sometimes formed basement membranes isolating partially the graft from the host parenchyma. During host myelination, astrocytes, which were present in most white matter structures, surrounded grafted cells. Occasionally, they enclosed Schwann cells in basement membranes or encircled host axons. Later, reactive astrocytes were associated with Schwann cells restricted to blood vessel and ventricular walls, and meninges. Our results suggest that in the presence of competitive developing oligodendrocytes, astrocytes are able to limit migration and prevent myelination of Schwann cells transplanted in the newborn shiverer brain. In addition, astrocytes seem to be able to expel the grafted cells and finally exclude them from the host parenchyma.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1396177     DOI: 10.1159/000111650

Source DB:  PubMed          Journal:  Dev Neurosci        ISSN: 0378-5866            Impact factor:   2.984


  8 in total

1.  Molecular reconstruction of nodes of Ranvier after remyelination by transplanted olfactory ensheathing cells in the demyelinated spinal cord.

Authors:  Masanori Sasaki; Joel A Black; Karen L Lankford; Hajime A Tokuno; Stephen G Waxman; Jeffery D Kocsis
Journal:  J Neurosci       Date:  2006-02-08       Impact factor: 6.167

2.  Comparison of cellular architecture, axonal growth, and blood vessel formation through cell-loaded polymer scaffolds in the transected rat spinal cord.

Authors:  Nicolas N Madigan; Bingkun K Chen; Andrew M Knight; Gemma E Rooney; Eva Sweeney; Lisa Kinnavane; Michael J Yaszemski; Peter Dockery; Timothy O'Brien; Siobhan S McMahon; Anthony J Windebank
Journal:  Tissue Eng Part A       Date:  2014-08-11       Impact factor: 3.845

Review 3.  Cellular transplantation strategies for spinal cord injury and translational neurobiology.

Authors:  Paul J Reier
Journal:  NeuroRx       Date:  2004-10

4.  GDNF modifies reactive astrogliosis allowing robust axonal regeneration through Schwann cell-seeded guidance channels after spinal cord injury.

Authors:  Ling-Xiao Deng; Jianguo Hu; Naikui Liu; Xiaofei Wang; George M Smith; Xuejun Wen; Xiao-Ming Xu
Journal:  Exp Neurol       Date:  2011-02-21       Impact factor: 5.330

5.  Astrocytes from cerebral cortex or striatum attract adult host serotoninergic axons into intrastriatal ventral mesencephalic co-grafts.

Authors:  A Petit; P Pierret; A Vallée; G Doucet
Journal:  J Neurosci       Date:  2001-09-15       Impact factor: 6.167

6.  Schwann cells are removed from the spinal cord after effecting recovery from paraplegia.

Authors:  L Jasmin; G Janni; T M Moallem; D A Lappi; P T Ohara
Journal:  J Neurosci       Date:  2000-12-15       Impact factor: 6.167

Review 7.  Olfactory ensheathing cells (OECs) and the treatment of CNS injury: advantages and possible caveats.

Authors:  Susan C Barnett; John S Riddell
Journal:  J Anat       Date:  2004-01       Impact factor: 2.610

Review 8.  Requirements for Schwann cell migration within CNS environments: a viewpoint.

Authors:  R J Franklin; W F Blakemore
Journal:  Int J Dev Neurosci       Date:  1993-10       Impact factor: 2.457

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.