Literature DB >> 9888988

Widespread integration and survival of adult-derived neural progenitor cells in the developing optic retina.

M Takahashi1, T D Palmer, J Takahashi, F H Gage.   

Abstract

Adult rat hippocampus-derived neural progenitor cells (AHPC) show considerable adaptability following grafting to several brain regions. To evaluate the plasticity of AHPCs within the optic retina, retrovirally engineered AHPCs were grafted into the vitreous cavity of the adult and newborn rat eye. Within the adult eye, AHPCs formed a uniform nondisruptive lamina in intimate contact with the inner limiting membrane. Within 4 weeks of grafting to the developing eye, the AHPCs were well integrated into the retina and adopted the morphologies and positions of Müller, amacrine, bipolar, horizontal, photoreceptor, and astroglial cells. Although the cells expressed neuronal or glial markers, none acquired end-stage markers unique to retinal neurons. This suggests that the adult-derived stem cells can adapt to a wide variety of heterologous environments and express some but not all features of retinal cells when exposed to the cues present late in retinal development. Copyright 1998 Academic Press.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9888988     DOI: 10.1006/mcne.1998.0721

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  64 in total

1.  Adult spinal cord stem cells generate neurons after transplantation in the adult dentate gyrus.

Authors:  L S Shihabuddin; P J Horner; J Ray; F H Gage
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

Review 2.  Basement membranes and artificial substrates in cell transplantation.

Authors:  Carl Sheridan; Rachel Williams; Ian Grierson
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2003-11-20       Impact factor: 3.117

3.  Therapy may yet stem from cells in the retina.

Authors:  R R Ali; J C Sowden
Journal:  Br J Ophthalmol       Date:  2003-09       Impact factor: 4.638

4.  Specification of the retinal fate of mouse embryonic stem cells by ectopic expression of Rx/rax, a homeobox gene.

Authors:  Yoko Tabata; Yasuo Ouchi; Haruyuki Kamiya; Toshiya Manabe; Ken-ichi Arai; Sumiko Watanabe
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

5.  Meteorin: a secreted protein that regulates glial cell differentiation and promotes axonal extension.

Authors:  Jinsuke Nishino; Kimiyo Yamashita; Hiromi Hashiguchi; Hideta Fujii; Takuya Shimazaki; Hiroshi Hamada
Journal:  EMBO J       Date:  2004-04-15       Impact factor: 11.598

Review 6.  Chondroitin sulfate "wobble motifs" modulate maintenance and differentiation of neural stem cells and their progeny.

Authors:  Anurag Purushothaman; Kazuyuki Sugahara; Andreas Faissner
Journal:  J Biol Chem       Date:  2011-11-17       Impact factor: 5.157

7.  Intrinsic differences among spatially distinct neural crest stem cells in terms of migratory properties, fate determination, and ability to colonize the enteric nervous system.

Authors:  Jack T Mosher; Kelly J Yeager; Genevieve M Kruger; Nancy M Joseph; Mark E Hutchin; Andrzej A Dlugosz; Sean J Morrison
Journal:  Dev Biol       Date:  2006-10-24       Impact factor: 3.582

Review 8.  Adult neurogenesis and cellular brain repair with neural progenitors, precursors and stem cells.

Authors:  U Shivraj Sohur; Jason G Emsley; Bartley D Mitchell; Jeffrey D Macklis
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-09-29       Impact factor: 6.237

9.  A microfabricated scaffold for retinal progenitor cell grafting.

Authors:  William L Neeley; Stephen Redenti; Henry Klassen; Sarah Tao; Tejal Desai; Michael J Young; Robert Langer
Journal:  Biomaterials       Date:  2007-10-24       Impact factor: 12.479

10.  CD133+ adult human retinal cells remain undifferentiated in Leukaemia Inhibitory Factor (LIF).

Authors:  Debra A Carter; Andrew D Dick; Eric J Mayer
Journal:  BMC Ophthalmol       Date:  2009-02-23       Impact factor: 2.209

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.