Measuring NLR Oligomerization II: Detection of ASC Speck Formation by Confocal Microscopy and Immunofluorescence

Methods Mol Biol. 2016:1417:145-58. doi: 10.1007/978-1-4939-3566-6_9.

Abstract

Inflammasome assembly results in the formation of a large intracellular protein scaffold driven by the oligomerization of the adaptor protein apoptosis-associated speck-like protein containing a CARD (ASC). Following inflammasome activation, ASC polymerizes to form a large singular structure termed the ASC "speck," which is crucial for recruitment of caspase-1 and its inflammatory activity. Hence, due to the considerably large size of these structures, ASC specks can be easily visualized by microscopy as a simple upstream readout for inflammasome activation. Here, we provide two detailed protocols for imaging ASC specks: by (1) live-cell imaging of monocyte/macrophage cell lines expressing a fluorescently tagged version of ASC and (2) immunofluorescence of endogenous ASC in cell lines and human immune cells. In addition, we outline a protocol for increasing the specificity of ASC antibodies for use in immunofluorescence.

Keywords: ASC; Confocal microscopy; Flow cytometry; Immunofluorescence; Inflammasome; Live-cell imaging; Speck.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CARD Signaling Adaptor Proteins / chemistry*
  • Caspase 1 / metabolism
  • Cells, Cultured
  • Fluorescent Antibody Technique
  • Humans
  • Inflammasomes / metabolism
  • Macrophages / cytology
  • Macrophages / metabolism
  • Mice
  • Microscopy, Confocal
  • Protein Multimerization
  • THP-1 Cells

Substances

  • CARD Signaling Adaptor Proteins
  • Inflammasomes
  • PYCARD protein, human
  • Pycard protein, mouse
  • Caspase 1