» Articles » PMID: 217018

Induction of Neurite Outgrowth by a Conditioned-medium Factor Bound to the Culture Substratum

Overview
Specialty Science
Date 1978 Oct 1
PMID 217018
Citations 34
Authors
Affiliations
Soon will be listed here.
Abstract

Heart-cell conditioned medium (HCM) induces rapid neurite outgrowth from isolated neurons in culture. The following evidence indicates that this action of HCM is due to a trypsin-sensitive factor which attaches to the polyornithinecoated culture substratum: (i) Pretreatment of the culture substratum with HCM allows rapid neurite outgrowth to occur even in unconditioned media. The active factor remains bound to the substratum during the period of neurite outgrowth. (ii) The substratum-bound activity is destroyed by trypsin treatment, but is insensitive to collagenase, RNase, and DNase. (iii) The factor that binds to the substratum is essential for neurite outgrowth, because HCM is no longer active when the material that binds to the polyornithine substratum has been removed by passage of the HCM over a series of culture dishes. However, this "depleted" HCM is still able to support the growth of nonneuronal cells. (iv) Most significantly, when neurons are cultured in whole HCM, the extent of neurite outgrowth is proportional to the amount of substratum-bound activity and not to the amount in solution, indicating that the substratum-bound form of the factor is more active. Previous observations [Collins, F. (1978) Dev. Biol. 65, 50-57] suggest that HCM promotes neurite outgrowth by increasing the adhesion between nerve cell surface extensions and the polyornithine-coated culture substratum. It is possible, therefore, that the factor in HCM that binds to the substratum possesses sites to which nerve cell surface components adhere.

Citing Articles

Muscle reinnervation and IGF-I synthesis are affected by exposure to heparin: an effect partially antagonized by anti-growth hormone-releasing hormone.

Madaschi L, Di Giulio A, Gorio A Neurochem Res. 2003; 28(1):163-8.

PMID: 12587674 DOI: 10.1023/a:1021616716463.


Isolation of a neural chondroitin sulfate proteoglycan with neurite outgrowth promoting properties.

Faissner A, Clement A, Lochter A, Streit A, Mandl C, Schachner M J Cell Biol. 1994; 126(3):783-99.

PMID: 7519189 PMC: 2120143. DOI: 10.1083/jcb.126.3.783.


Rapid retraction of neurites by sensory neurons in response to increased concentrations of nerve growth factor.

GRIFFIN C, Letourneau P J Cell Biol. 1980; 86(1):156-61.

PMID: 7191423 PMC: 2110643. DOI: 10.1083/jcb.86.1.156.


Elongating nerve fibers are guided by a pathway of material released from embryonic nonneuronal cells.

Collins F, Garrett Jr J Proc Natl Acad Sci U S A. 1980; 77(10):6226-8.

PMID: 6934547 PMC: 350248. DOI: 10.1073/pnas.77.10.6226.


Isolation and characterization of a large, neurite-associated glycoconjugate from neuroblastoma cells.

Chernoff E, Maresh G, Culp L J Cell Biol. 1983; 96(3):661-8.

PMID: 6833376 PMC: 2112426. DOI: 10.1083/jcb.96.3.661.


References
1.
Helfand S, Riopelle R, Wessells N . Non-equivalence of conditioned medium and nerve growth factor for sympathetic, parasympathetic, and sensory neurons. Exp Cell Res. 1978; 113(1):39-45. DOI: 10.1016/0014-4827(78)90085-x. View

2.
Grinnell F . Cellular adhesiveness and extracellular substrata. Int Rev Cytol. 1978; 53:65-144. DOI: 10.1016/s0074-7696(08)62241-x. View

3.
Levenson R . A collagen film microassay for tissue collagenase. Anal Biochem. 1976; 76(2):579-88. DOI: 10.1016/0003-2697(76)90352-3. View

4.
Nishi R, Berg D . Dissociated ciliary ganglion neurons in vitro: survival and synapse formation. Proc Natl Acad Sci U S A. 1977; 74(11):5171-5. PMC: 432123. DOI: 10.1073/pnas.74.11.5171. View

5.
Collins F . Axon initiation by ciliary neurons in culture. Dev Biol. 1978; 65(1):50-7. DOI: 10.1016/0012-1606(78)90178-1. View