Access the full text.
Sign up today, get DeepDyve free for 14 days.
Alfred MacConkey (1914)
TETANUSBritish Medical Journal, 2
G. Lee, E. Grollman, S. Dyer, F. Beguinot, L. Kohn, W. Habig, M. Hardegree (1979)
Tetanus toxin and thyrotropin interactions with rat brain membrane preparations.The Journal of biological chemistry, 254 10
F. Ambesi-Impiombato, L. Parks, H. Coon (1980)
Culture of hormone-dependent functional epithelial cells from rat thyroids.Proceedings of the National Academy of Sciences of the United States of America, 77 6
K. McCarthy, J. Vellis (1980)
Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissueThe Journal of Cell Biology, 85
E. Yavin, Z. Yavin (1979)
Ganglioside Profiles during Neural Tissue DevelopmentDevelopmental Neuroscience, 2
E. Yavin, Z. Yavin, W. Habig, M. Hardegree, L. Kohn (1981)
Tetanus toxin association with developing neuronal cell cultures. Kinetic parameters and evidence for ganglioside-mediated internalization.The Journal of biological chemistry, 256 13
Dimpfel Dimpfel, Neale Neale, Haberman Haberman (1975)
125 I‐Labeled tetanus toxin as a neuronal marker in tissue culture derived from embryonic CNSNaunyn‐Schmiedebergs Arch Pharmakol Exp Pathol, 290
R. Mirsky, L. Wendon, Philippa Black, C. Stolkin, D. Bray (1978)
Tetanus toxin: a cell surface marker for neurones in cultureBrain Research, 148
C. Schengrund, M. Repman (1977)
Cell culture of sixteen‐day‐old rat embryo cerebra and associated changes in ganglioside patternJournal of Neurochemistry, 29
D. Price, Jack Griffin, A. Young, K. Peck, Adelaine Stocks (1975)
Tetanus toxin: direct evidence for retrograde intraaxonal transport.Science, 188 4191
J. Mellanby, D. Pope (1976)
The relationship between the action of tetanus toxin and its binding by membranes and gangliosides.Advances in experimental medicine and biology, 71
F. Ledley, G. Lee, L. Kohn, W. Habig, M. Hardegree (1977)
Tetanus toxin interactions with thyroid plasma membranes. Implications for structure and function of tetanus toxin receptors and potential pathophysiological significance.The Journal of biological chemistry, 252 12
Yavin Yavin, Yavin Yavin (1979)
Ganglioside profiles during neural tissue development: Acquisition in the prenatal rat brain and cerebral cell culturesDev Neurosci, 2
A. Turpin, M. Raynaud (1959)
[Tetanus toxin].Annales de l'Institut Pasteur, 97
W. Dimpfel, E. Habermann (1977)
Binding characteristics of 125I-labelled tetanus toxin to primary tissue cultures from mouse embryonic CNS.Journal of neurochemistry, 29 6
J. Bottenstein, G. Sato (1979)
Growth of a rat neuroblastoma cell line in serum-free supplemented medium.Proceedings of the National Academy of Sciences of the United States of America, 76 1
K. Burton (1968)
[105] Determination of DNA concentration with diphenylamineMethods in Enzymology, 12
Z. Yavin, E. Yavin (1980)
Survival and maturation of cerebral neurons on poly(L-lysine) surfaces in the absence of serum.Developmental biology, 75 2
T. Rogers, Solomon Snyder (1981)
High affinity binding of tetanus toxin to mammalian brain membranes.The Journal of biological chemistry, 256 5
A. Ben-Ze'ev, A. Duerr, F. Solomon, S. Penman (1979)
The outer boundary of the cytoskeleton: a lamina derived from plasma membrane proteinsCell, 17
K. Stöckel, M. Schwab, H. Thoenen (1975)
Comparison between the retrograde axonal transport of nerve growth factor and tetanus toxin in motor, sensory and adrenergic neuronsBrain Research, 99
P. Honegger, D. Lenoir, P. Favrod (1979)
Growth and differentiation of aggregating fetal brain cells in a serum-free defined mediumNature, 282
Cultivation of pure populations of cerebral cells and the unambiguous identification of the neuronal and glial elements is a prerequisite for studying biochemical parameters associated with the developing nervous system under in vitro controlled conditions. We now report on sequestration of tetanus toxin, an exclusive marker for the neuronal cell surface, into a cellular compartment which prevents its release by neuraminidase. This compartment is associated with cellular elements remaining after detergent extraction of neuronal cells grown in monolayer cultures. Toxin sequestration into this compartment is preceded by a neuraminidase‐sensitive receptor mediated binding process which can be correlated with the appearance of lipid‐bound sialic acid in developing neuronal cultures.
Journal of Neuroscience Research – Wiley
Published: Jan 1, 1982
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.