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Slice Cultures for Study of Microglia

  • Carol A. Colton
  • Meggan Czapiga
  • Toby N. Behar
Protocol
  • 2.8k Downloads
Part of the Springer Protocols Handbooks book series (SPH)

Abstract

Culture of isolated microglia from dissociated cortical tissue has promoted the in vitro study of microglial function and morphological characteristics (Giulian and Baker, 1986; Streit and Kincaid-Colton, 1995). However, cultures prepared in this manner demonstrate characteristic “ameboid” morphology, and are generally considered to be more activated than the normal, resting microglia found in situ (Sedgwick et al., 1991). To reduce this problem, as well as to recreate a cellular architecture more typical of in vivo conditions, we have utilized an organotypic tissue slice method for culture of microglia (Czapiga and Colton, 1999; Gahwiler et al., 1997). This technique allows visualization of microglial morphology and the determination of certain microglial functional parameters, in a culture environment more reminiscent of the in vivo brain.

Keywords

Slice Culture Multiwell Plate Membrane Insert Propidium Iodide Solution Microglial Function 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Further Reading

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Copyright information

© Humana Press Inc., Totowa, NJ 2001

Authors and Affiliations

  • Carol A. Colton
    • 1
  • Meggan Czapiga
    • 2
  • Toby N. Behar
    • 3
  1. 1.Division of NeurologyDuke University Medical CenterDurham
  2. 2.Physiology DepartmentGeorgetown University Medical SchoolWashington, DC
  3. 3.Laboratory of Neurophysiology, National Institute for Neurological Disorders and StrokeNational Institutes of HealthBethesda

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