A herpes simplex viral vector expressing green fluorescent protein can be used to visualize morphological changes in high-density neuronal culture

Torsten Falk, Lori A. Strazdas, Rebecca S. Borders, Ramsey K. Kilani, Andrea J. Yool, Scott J Sherman

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

High-density cultures of mammalian neurons offer a model system for studies of brain development, but the morphological features of individual neurons is difficult to ascertain. We show that a herpes virus vector expressing a bioluminescent protein allows detailed morphometric analyses of living neurons in complex culture environments. Expression of enhanced green fluorescent protein (eGFP) was constitutively driven in neurons using the herpes simplex virus amplicon system. This system allowed us to make novel observations regarding development in high-density cultures from rat hippocampus and cerebellum. After the phase of initial neurite outgrowth, maturing neurons continue to show rapid remodeling of the neurite branches (0.79 ± 0.11 μm/h per neurite; mean ± SEM, n=8), and displacement of the soma within the neurite arbor (1.35 ± 0.74 μm/h). These results demonstrate that a substantial capacity for morphological plasticity persists in maturing mammalian CNS neurons after cessation of net neurite outgrowth in early development.

Original languageEnglish (US)
Pages (from-to)33-45
Number of pages13
JournalElectronic Journal of Biotechnology
Volume4
Issue number1
StatePublished - 2001

Fingerprint

Herpes Simplex
Green Fluorescent Proteins
Neurons
Neurites
Luminescent Proteins
Carisoprodol
Simplexvirus
Cerebellum
Hippocampus
Viruses
Brain

Keywords

  • Cerebellum
  • Green fluorescent protein
  • Hippocampus
  • Plasticity
  • Purkinje neuron

ASJC Scopus subject areas

  • Biotechnology
  • Applied Microbiology and Biotechnology

Cite this

A herpes simplex viral vector expressing green fluorescent protein can be used to visualize morphological changes in high-density neuronal culture. / Falk, Torsten; Strazdas, Lori A.; Borders, Rebecca S.; Kilani, Ramsey K.; Yool, Andrea J.; Sherman, Scott J.

In: Electronic Journal of Biotechnology, Vol. 4, No. 1, 2001, p. 33-45.

Research output: Contribution to journalArticle

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AU - Sherman, Scott J

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AB - High-density cultures of mammalian neurons offer a model system for studies of brain development, but the morphological features of individual neurons is difficult to ascertain. We show that a herpes virus vector expressing a bioluminescent protein allows detailed morphometric analyses of living neurons in complex culture environments. Expression of enhanced green fluorescent protein (eGFP) was constitutively driven in neurons using the herpes simplex virus amplicon system. This system allowed us to make novel observations regarding development in high-density cultures from rat hippocampus and cerebellum. After the phase of initial neurite outgrowth, maturing neurons continue to show rapid remodeling of the neurite branches (0.79 ± 0.11 μm/h per neurite; mean ± SEM, n=8), and displacement of the soma within the neurite arbor (1.35 ± 0.74 μm/h). These results demonstrate that a substantial capacity for morphological plasticity persists in maturing mammalian CNS neurons after cessation of net neurite outgrowth in early development.

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