Morphology-based non-invasive quantitative prediction of the differentiation status of neural stem cells

2017 
Neural stem cells (NSCs) are multipotent and are considered ideal source for regenerating damaged neural cells for neurological disorders. During culture of NSCs, both the measurement and the evaluation of their differentiation potential are important to maintain stable quality-assured NSCs for regenerative treatments since the rate of differentiation into certain lineages from NSCs is still not fully controllable. However, conventional cell evaluation techniques using biological molecular are still invasive, costly, and time-consuming. Therefore, a non-invasive, low-cost, and rapid cell evaluation method is required to expand the possibilities of regenerative therapy, especially in the facilities that produce cells for therapy. To address these such technological limitations in non-invasive cell evaluation, we propose the efficacy of computer-aided morphology-based prediction of potentials of stem cells by using multiple and time-course morphological parameters from phase-contrast microscopic images combined with experimentally determined differentiation potentials. In this work, we quantified the morphological parameters of NSCs during three types of differentiation culture and investigated two applications with NSCs: (i) evaluation of their differentiation type and (ii) early prediction of neural differentiation rate. Our data demonstrate that it is possible to non-invasively evaluate neural differentiation types and quantitatively predict future differentiation rates by using morphological information from the first 4 days. Our findings indicate the potential application of morphology-based non-invasive evaluation for optimizing effective differentiation protocols, screening of compounds to mediate NSC differentiation, and quality maintenance of regenerative medicine products.
    • Correction
    • Source
    • Cite
    • Save
    • Machine Reading By IdeaReader
    24
    References
    10
    Citations
    NaN
    KQI
    []