Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

A modified silver method for demonstrating developing nervous tissue in culture.

P E Spoerri, H C Ludwig, Y Ogawa

    Acta Anatomica
    |January 1, 1985
    PubMed
    Summary
    This summary is machine-generated.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Hydrocephalus shunt therapy: current titanium shunt valve implants obstructed by internal tissue proliferations identified as extracellular matrix membranes.

    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery·2019
    Same author

    Effects of gangliosides on the in vitro development of neuroblastoma cells: An ultrastructural study.

    International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience·2014
    Same author

    Syntheses in the pyrazine series; the preparation and properties of the pyrazyl halides.

    Journal of the American Chemical Society·2010
    Same author

    Syntheses in the pyrazine series; preparation of 2,5-dicyanopyrazine and the diacetyl diamide of pyrazine dicarboxylic acid-2,5.

    Journal of the American Chemical Society·2010
    Same author

    Differences between substrate specificities of l-glutamate uptake by neurons and glia, studied in cell lines and primary cultures.

    Neurochemistry international·2010
    Same author

    The pyrazines.

    Chemical reviews·2010
    Same journal

    Degeneration and regeneration of the testicles, taking particular account of the effects of gynecogenic and androgenic active substances on male gonads of mature albino rats.

    Acta anatomica·2010
    Same journal

    Arteriovenous anastomoses in the endometrium in man.

    Acta anatomica·2010
    Same journal

    The sympathetic innervation of the glands.

    Acta anatomica·2010
    Same journal

    How to conceive of anatomy, its teaching and its research.

    Acta anatomica·2010
    Same journal

    Experiments into the action of testosterone propionate on the kidneys of male rabbits.

    Acta anatomica·2010
    Same journal

    Retina studies.

    Acta anatomica·2010
    See all related articles

    Primary chick cerebrum neuron cultures showed differentiated morphology and a complex neurofibrillary network after 2 weeks in vitro. Specialized silver staining confirmed neuron structure and ramification over 18 days.

    Area of Science:

    • Neuroscience
    • Developmental Biology
    • Cell Culture

    Background:

    • Understanding neuronal development is crucial for neuroscience.
    • Primary neuronal cultures offer a model for studying neural differentiation.
    • Embryonic chick cerebrum provides a well-established system for neural development research.

    Purpose of the Study:

    • To characterize the morphological differentiation of primary neurons from embryonic chick cerebrum in vitro.
    • To investigate the development of the neurofibrillary network in cultured neurons.
    • To validate a modified silver impregnation technique for visualizing neuronal structures.

    Main Methods:

    • Dissociated explants of 8-day-old embryonic chick cerebrum were cultured for up to 18 days.
    • Morphological changes were observed over time.

    Related Experiment Videos

  • A modified silver impregnation method with potassium ferrocyanide was used for neuron visualization.
  • Main Results:

    • Primary neuron cultures exhibited characteristic differentiated morphology by the second week of culture.
    • An increasingly ramified and interconnecting neurofibrillary network developed over time.
    • Neurons of various morphologies (bipolar, tripolar, multipolar) were successfully stained.

    Conclusions:

    • Embryonic chick cerebrum neurons in primary culture undergo significant morphological differentiation.
    • A complex neurofibrillary network forms in vitro, mirroring in vivo development.
    • The modified silver impregnation technique is effective for demonstrating differentiated neuronal morphology.