Literature DB >> 19441921

Cryopreservation of early postmitotic neuronal cells in culture.

Philippe Taupin1.   

Abstract

BACKGROUND: The application is in the field of embryonic stem cells (ESCs) and the cryopreservation of neuronal cells in culture.
OBJECTIVE: It aims at establishing conditions for the cryopreservation of cultured neuronal cells readily usable, upon thawing. That is cryopreserved neuronal cells with a high rate of survivability and with a potential to differentiate into mature neuronal cells rapidly, after thawing.
METHODS: Neuronal precursor cells and neuronal cells were generated in vitro, from cultures of human ESCs (hESCs). Neuronal cells were frozen and cryopreserved at a stage when they begin to express neuronal class III beta-tubulin. RESULTS/
CONCLUSION: The application claims that neuronal cells elicit a rate of survivability greater than 50% and neurites outgrowth within 10 to 14 hours, after thawing. The cryopreservation of post-mitotic neuronal or neural-like cells provides a source of nerve cells readily usable for research and therapy.

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Year:  2009        PMID: 19441921     DOI: 10.1517/13543770802688891

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  1 in total

1.  Freshly frozen E18 rat cortical cells can generate functional neural networks after standard cryopreservation and thawing procedures.

Authors:  Kim Quasthoff; Stefano Ferrea; Wiebke Fleischer; Stephan Theiss; Alfons Schnitzler; Marcel Dihné; Janine Walter
Journal:  Cytotechnology       Date:  2014-02-23       Impact factor: 2.058

  1 in total

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