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Glial growth factor 2 induces proliferation and structural changes in ensheathing cells
M I Chuah1, J Cossins, E Woodhall
1Department of Anatomy and Physiology, University of Tasmania, Box 252-24, Hobart, Australia. inn.chuah@utas.edu.au
Brain Research
|March 4, 2000
Summary
Glial growth factor 2 (GGF2) modestly increased ensheathing cell proliferation at lower doses, promoting structural changes and extracellular matrix deposition. Ensheathing cells also appear to produce GGF2, suggesting an autocrine role.
Area of Science:
- Neuroscience
- Cell Biology
- Developmental Biology
Background:
- Olfactory bulb ensheathing cells play a crucial role in nerve development and myelination.
- Glial growth factor 2 (GGF2) is a known regulator of neural cell development.
Purpose of the Study:
- To investigate the effects of GGF2 on neonatal rat olfactory bulb ensheathing cell proliferation and structure.
- To determine if GGF2 acts as a chemoattractant for ensheathing cells.
- To explore the potential autocrine production of GGF2 by ensheathing cells.
Main Methods:
- Cell culture of neonatal rat olfactory bulb ensheathing cells.
- Proliferation assays to assess cell growth in response to GGF2.
- Chemotaxis assays and scanning electron microscopy to evaluate cell migration and structural changes.
- Reverse transcription-polymerase chain reaction (RT-PCR) to detect GGF2 gene expression.
Main Results:
- GGF2 induced a modest increase in ensheathing cell proliferation at concentrations up to 60 ng/ml, but not at higher doses.
- No chemotactic response of ensheathing cells to GGF2 was observed.
- GGF2 promoted structural changes, including increased extracellular matrix deposition and enhanced cytoskeletal support, leading to more rigid cell processes.
- RT-PCR confirmed the presence of GGF2 transcripts in ensheathing cells.
Conclusions:
- GGF2 influences the proliferation and structural integrity of olfactory bulb ensheathing cells.
- Ensheathing cells may utilize GGF2 in an autocrine manner for self-regulation.
- GGF2's role extends beyond chemoattraction, impacting cell morphology and support structures.