Skip to main content

Advertisement

Log in

Nestin expression – a property of multi-lineage progenitor cells?

  • Review
  • Published:
Cellular and Molecular Life Sciences CMLS Aims and scope Submit manuscript

Abstract.

Tissue-specific progenitor cells are characterized by proliferation and differentiation, but, in contrast to embryonic stem (ES) cells, have limited capacities for self-renewal and no tumourigenic potential. These latter traits make progenitor cells an ideal source for regenerative cell therapies. In this review, we describe what is currently known about nestin, an intermediate filament first identified in neuroepithelial stem cells. During embryogenesis, nestin is expressed in migrating and proliferating cells, whereas in adult tissues, nestin is mainly restricted to areas of regeneration. We show that nestin is abundant in ES-derived progenitor cells that have the potential to develop into neuroectodermal, endodermal and mesodermal lineages. Although it remains unclear what factors regulate in vitro and in vivo expression of nestin, we conclude that nestin represents a characteristic marker of multi-lineage progenitor cells and suggest that its presence in cells may indicate multi-potentiality and regenerative potential.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. M. Wobus.

Additional information

Received 1 April 2004; received after revision 17 May 2004; accepted 8 June 2004

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wiese, C., Rolletschek, A., Kania, G. et al. Nestin expression – a property of multi-lineage progenitor cells?. CMLS, Cell. Mol. Life Sci. 61, 2510–2522 (2004). https://doi.org/10.1007/s00018-004-4144-6

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00018-004-4144-6

Key words.

Navigation