Regulation of prenatal human retinal neurosphere growth and cell fate potential by retinal pigment epithelium and Mash1

David M. Gamm, Lynda S. Wright, Elizabeth E. Capowski, Rebecca L. Shearer, Jason S. Meyer, Hyun Jung Kim, Bernard L. Schneider, John Nicholas Melvan, Clive N. Svendsen

Research output: Contribution to journalArticle

Abstract

During development of the central nervous system, stem and progenitor cell proliferation and differentiation are controlled by complex inter- and intracellular interactions that orchestrate the precise spatiotemporal production of particular cell types. Within the embryonic retina, progenitor cells are located adjacent to the retinal pigment epithelium (RPE), which differentiates prior to the neurosensory retina and has the capacity to secrete a multitude of growth factors. We found that secreted proteinaceous factors in human prenatal RPE conditioned medium (RPE CM) prolonged and enhanced the growth of human prenatal retinal neurospheres. The growth-promoting activity of RPE CM was mitogen-dependent and associated with an acute increase in transcription factor phosphorylation. Expanded populations of RPE CM-treated retinal neurospheres expressed numerous neurodevelopmental and eye specification genes and markers characteristic of neural and retinal progenitor cells, but gradually lost the potential to generate neurons upon differentiation. Misexpression of Mash1 restored the neurogenic potential of long-term cultures, yielding neurons with phenotypic characteristics of multiple inner retinal cell types. Thus, a novel combination of extrinsic and intrinsic factors was required to promote both progenitor cell proliferation and neuronal multipotency in human retinal neurosphere cultures. These results support a pro-proliferative and antiapoptotic role for RPE in human retinal development, reveal potential limitations of human retinal progenitor culture systems, and suggest a means for overcoming cell fate restriction in vitro.

Original languageEnglish (US)
Pages (from-to)3182-3193
Number of pages12
JournalStem Cells
Volume26
Issue number12
DOIs
StatePublished - Dec 1 2008
Externally publishedYes

Fingerprint

Retinal Pigment Epithelium
Stem Cells
Growth
Retina
Cell Proliferation
Neurons
Intrinsic Factor
Human Development
Conditioned Culture Medium
Mitogens
Cell Differentiation
Intercellular Signaling Peptides and Proteins
Transcription Factors
Central Nervous System
Phosphorylation
Population
Genes

Keywords

  • Conditioned medium
  • Culture
  • Differentiation
  • Human
  • Mash1
  • Retinal pigment epithelium
  • Retinal progenitor cells

ASJC Scopus subject areas

  • Molecular Medicine
  • Developmental Biology
  • Cell Biology

Cite this

Gamm, D. M., Wright, L. S., Capowski, E. E., Shearer, R. L., Meyer, J. S., Kim, H. J., ... Svendsen, C. N. (2008). Regulation of prenatal human retinal neurosphere growth and cell fate potential by retinal pigment epithelium and Mash1. Stem Cells, 26(12), 3182-3193. https://doi.org/10.1634/stemcells.2008-0300

Regulation of prenatal human retinal neurosphere growth and cell fate potential by retinal pigment epithelium and Mash1. / Gamm, David M.; Wright, Lynda S.; Capowski, Elizabeth E.; Shearer, Rebecca L.; Meyer, Jason S.; Kim, Hyun Jung; Schneider, Bernard L.; Melvan, John Nicholas; Svendsen, Clive N.

In: Stem Cells, Vol. 26, No. 12, 01.12.2008, p. 3182-3193.

Research output: Contribution to journalArticle

Gamm, DM, Wright, LS, Capowski, EE, Shearer, RL, Meyer, JS, Kim, HJ, Schneider, BL, Melvan, JN & Svendsen, CN 2008, 'Regulation of prenatal human retinal neurosphere growth and cell fate potential by retinal pigment epithelium and Mash1', Stem Cells, vol. 26, no. 12, pp. 3182-3193. https://doi.org/10.1634/stemcells.2008-0300
Gamm, David M. ; Wright, Lynda S. ; Capowski, Elizabeth E. ; Shearer, Rebecca L. ; Meyer, Jason S. ; Kim, Hyun Jung ; Schneider, Bernard L. ; Melvan, John Nicholas ; Svendsen, Clive N. / Regulation of prenatal human retinal neurosphere growth and cell fate potential by retinal pigment epithelium and Mash1. In: Stem Cells. 2008 ; Vol. 26, No. 12. pp. 3182-3193.
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