Literature DB >> 2351964

Developmental maps of acetylcholinesterase and G4-antigen of the early chicken brain: long-distance tracts originate from AChE-producing cell bodies.

T Weikert1, F G Rathjen, P G Layer.   

Abstract

After approaching the outer surface of the neuroepithelium, postmitotic cell bodies abruptly start to synthesize acetylcholinesterase (AChE). Their easy histochemical detection allows us to trace sensitively spatiotemporal patterns of differentiation processes of the chicken nervous system. To investigate the relationship between postmitotic AChE production and the first formation of neurites, AChE histochemistry is combined here with immunohistochemistry using the neurite-specific G4-antibody. Spatial computer reconstructions from double-stained serial sections of whole brains of H.H. stages 10-20 demonstrate that G4-neurite expression spatio-temporally follows the expression of AChE in its complex polycentric pattern closely, the details of which have been described earlier. By comparing both differentiative steps at the single cell level reveals that a great majority (if not all) of the G4-positive neurites originate from AChE-positive cell bodies. Based on both the computer reconstructions as well as single cell analysis, including [3H]-thymidine pulse-experiments followed by autoradiography, we conclude, that AChE expression precedes formation of G4-neurites by about 15 h. In addition, the reconstructions provide the first detailed maps of G4-fiber tract formation and shows that G4-neurites form fascicles, most of which travel over long distances to targets within or without the central nervous system (CNS). This is the first demonstration for the entire young chicken brain which verifies that AChE-expressing cells, generally, are those that will establish efferents to distant targets.

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Year:  1990        PMID: 2351964     DOI: 10.1002/neu.480210309

Source DB:  PubMed          Journal:  J Neurobiol        ISSN: 0022-3034


  9 in total

1.  Contraction and stress-dependent growth shape the forebrain of the early chicken embryo.

Authors:  Kara E Garcia; Ruth J Okamoto; Philip V Bayly; Larry A Taber
Journal:  J Mech Behav Biomed Mater       Date:  2016-08-15

2.  Cranial nerve growth in birds is preceded by cholinesterase expression during neural crest cell migration and the formation of an HNK-1 scaffold.

Authors:  P G Layer; S Kaulich
Journal:  Cell Tissue Res       Date:  1991-09       Impact factor: 5.249

Review 3.  Cholinesterases during development of the avian nervous system.

Authors:  P G Layer
Journal:  Cell Mol Neurobiol       Date:  1991-02       Impact factor: 5.046

4.  Chicken retinospheroids as developmental and pharmacological in vitro models: acetylcholinesterase is regulated by its own and by butyrylcholinesterase activity.

Authors:  P G Layer; T Weikert; E Willbold
Journal:  Cell Tissue Res       Date:  1992-06       Impact factor: 5.249

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

Authors:  P G Layer; T Weikert; R Alber
Journal:  Cell Tissue Res       Date:  1993-08       Impact factor: 5.249

6.  Cholinesterases and peanut agglutinin binding related to cell proliferation and axonal growth in embryonic chick limbs.

Authors:  R Alber; O Sporns; T Weikert; E Willbold; P G Layer
Journal:  Anat Embryol (Berl)       Date:  1994-11

7.  Morphogenic role for acetylcholinesterase in axonal outgrowth during neural development.

Authors:  J W Bigbee; K V Sharma; J J Gupta; J L Dupree
Journal:  Environ Health Perspect       Date:  1999-02       Impact factor: 9.031

8.  Fish E587 glycoprotein, a member of the L1 family of cell adhesion molecules, participates in axonal fasciculation and the age-related order of ganglion cell axons in the goldfish retina.

Authors:  M Bastmeyer; H Ott; C A Leppert; C A Stuermer
Journal:  J Cell Biol       Date:  1995-08       Impact factor: 10.539

9.  Acetylcholinesterase Regulates Skeletal In Ovo Development of Chicken Limbs by ACh-Dependent and -Independent Mechanisms.

Authors:  Janine Spieker; Anica Ackermann; Anika Salfelder; Astrid Vogel-Höpker; Paul G Layer
Journal:  PLoS One       Date:  2016-08-30       Impact factor: 3.240

  9 in total

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