Literature DB >> 8340814

Vacuole dynamics in growth cones: correlated EM and video observations.

M E Dailey1, P C Bridgman.   

Abstract

The neuronal growth cone is a major site of surface membrane dynamics associated with uptake and release of materials, motility, and axon extension. Although intracellular membrane organelles are thought to mediate surface membrane addition and retrieval at the growth cone, membrane events are fleeting and therefore difficult to study directly. In an effort to capture transient interactions between intracellular membrane organelles and the plasmalemma at the growth cone, embryonic rat sympathetic neuron cultures were prepared for whole-mount electron microscopy (EM) by rapid freezing and freeze substitution. We identified a set of vacuole-like organelles (> or = 150 nm in diameter) that appeared to interact directly with the plasmalemma. In stereo-pair EM images the bounding membrane of some of these vacuoles had an orifice at sites where the organelle was adjoining the plasmalemma, suggesting that the organelle and surface membranes were confluent. Since this population of organelles could be labeled with cationized ferritin or HRP when added to living cultures just prior to freezing or chemical fixation, they were probably derived from the plasmalemma. Combined light microscopy and EM of individual growth cones showed that these same vacuoles had a conspicuous reverse shadowcast appearance in differential interference contrast images. Thus, we used real-time video microscopy to follow these organelles in living growth cones. Many of these vacuoles spontaneously appeared, remained visible for several minutes, and then disappeared. Reverse shadowcast vacuoles were formed at various sites throughout the growth cone, including surface membrane ruffles at the leading edge [P (peripheral)-domain] as well as quiescent and retracting regions at the growth cone base [C (central)-domain]. Vacuoles in the P-domain moved centripetally and rarely grew in size. In contrast, those in the C-domain exhibited Brownian-like movements and sometimes appeared to increase in size, raising the possibility that new membrane may be added to these organelles. Vacuoles within both the P- and C-domains shrank before rapidly disappearing, but rarely vesiculated, suggesting that they had fused with the plasmalemma. The results indicate that vacuoles are a highly dynamic population of organelles that directly communicate with the plasma membrane at the growth cone; they provide a major route of surface membrane uptake and may also play a role in membrane recycling.

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Year:  1993        PMID: 8340814      PMCID: PMC6576535     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  16 in total

1.  Recycling of the cell adhesion molecule L1 in axonal growth cones.

Authors:  H Kamiguchi; V Lemmon
Journal:  J Neurosci       Date:  2000-05-15       Impact factor: 6.167

2.  The spectrin skeleton of newly-invaginated plasma membrane.

Authors:  T L Herring; P Juranka; J Mcnally; H Lesiuk; C E Morris
Journal:  J Muscle Res Cell Motil       Date:  2000-01       Impact factor: 2.698

3.  Membrane recycling in the neuronal growth cone revealed by FM1-43 labeling.

Authors:  T J Diefenbach; P B Guthrie; H Stier; B Billups; S B Kater
Journal:  J Neurosci       Date:  1999-11-01       Impact factor: 6.167

4.  TUC-4b, a novel TUC family variant, regulates neurite outgrowth and associates with vesicles in the growth cone.

Authors:  Christopher C Quinn; Esteban Chen; Tashi G Kinjo; Gail Kelly; Alexander W Bell; Robert C Elliott; Peter S McPherson; Susan Hockfield
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

5.  The soluble N-ethylmaleimide-sensitive factor attached protein receptor complex in growth cones: molecular aspects of the axon terminal development.

Authors:  M Igarashi; M Tagaya; Y Komiya
Journal:  J Neurosci       Date:  1997-02-15       Impact factor: 6.167

6.  Polymerizing microtubules activate site-directed F-actin assembly in nerve growth cones.

Authors:  M W Rochlin; M E Dailey; P C Bridgman
Journal:  Mol Biol Cell       Date:  1999-07       Impact factor: 4.138

7.  Particles move along actin filament bundles in nerve growth cones.

Authors:  L L Evans; P C Bridgman
Journal:  Proc Natl Acad Sci U S A       Date:  1995-11-21       Impact factor: 11.205

8.  Discrete and reversible vacuole-like dilations induced by osmomechanical perturbation of neurons.

Authors:  C Reuzeau; L R Mills; J A Harris; C E Morris
Journal:  J Membr Biol       Date:  1995-05       Impact factor: 1.843

9.  Dynamic organization of endocytic pathways in axons of cultured sympathetic neurons.

Authors:  C C Overly; P J Hollenbeck
Journal:  J Neurosci       Date:  1996-10-01       Impact factor: 6.167

10.  Studies on the development and behavior of the dystrophic growth cone, the hallmark of regeneration failure, in an in vitro model of the glial scar and after spinal cord injury.

Authors:  Veronica J Tom; Michael P Steinmetz; Jared H Miller; Catherine M Doller; Jerry Silver
Journal:  J Neurosci       Date:  2004-07-21       Impact factor: 6.167

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