English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Cholinesterases regulate neurite growth of chick nerve cells in vitro by means of a non-enzymatic mechanism

Layer, P., Weikert, T., & Alber, R. (1993). Cholinesterases regulate neurite growth of chick nerve cells in vitro by means of a non-enzymatic mechanism. Cell and Tissue Research, 273(2), 219-226. doi:10.1007/BF00312823.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Layer, PG1, Author           
Weikert, T1, Author           
Alber, R1, Author           
Affiliations:
1Department Molecular Biology Gierer, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3404872              

Content

show
hide
Free keywords: -
 Abstract: Cholinesterases present homologies with some cell adhesion molecules; however, it is unclear whether and how they perform adhesive functions. Here, we provide the first direct evidence showing that neurite growth in vitro from various neuronal tissues of the chick embryo can be modified by some, but not all, anticholinesterase agents. By quantifying the neuritic G4 antigen in tectal cell cultures, the effect of anticholinesterases on neurite growth is directly compared with their cholinesterase inhibitory action. BW 284C51 and ethopropazine, inhibiting acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), respectively, strongly decrease neurite growth in a dose-dependent manner. However, echothiophate which inhibits both cholinesterases, does not change neuritic growth. These quantitative data are supplemented by morphological observations in retinal explant cultures grown on striped laminin carpets, viz., defasciculation of neurite bundles by BW 284C51 and Bambuterol occurs, indicating that these drugs disturb adhesive mechanisms. These data strongly suggest that a) cholinesterases can participate in regulating axonal growth, b) both AChE and BChE can perform such a nonsynaptic function, and c) this function is not the result of the enzyme activity per se, since at least one drug was found that inhibits all cholinesterase activities but not neurite growth. Thus, a secondary site on cholinesterase molecules must be responsible for adhesive functions.

Details

show
hide
Language(s):
 Dates: 1993-08
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1007/BF00312823
PMID: 8103422
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Cell and Tissue Research
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Heidelberg : Springer-Verlag
Pages: - Volume / Issue: 273 (2) Sequence Number: - Start / End Page: 219 - 226 Identifier: ISSN: 0302-766X
CoNE: https://pure.mpg.de/cone/journals/resource/991042749577550