Tracking Plasma Cell Differentiation in Living Mice with Two-Photon Microscopy

Methods Mol Biol. 2017:1623:37-50. doi: 10.1007/978-1-4939-7095-7_3.

Abstract

Due to the multitude of cell types involved in the differentiation of plasma cells during the germinal center reaction, and due to a lack of in vitro systems, which recapitulate germinal centers, the most suitable way to study plasma cell generation in germinal centers is in vivo. In this chapter we describe how to induce humoral immune responses to defined model antigens and how to visualize and track plasma cells and their interactions with other cells in the lymph nodes of living mice.

Keywords: B cells; Fluorescent reporter mice; Germinal center; Intravital imaging; Lymph node; Plasma cells; Two-photon microscopy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • B-Lymphocytes / transplantation
  • Cell Differentiation*
  • Cell Tracking* / methods
  • Fluorescent Antibody Technique
  • Germinal Center / cytology
  • Germinal Center / immunology
  • Germinal Center / metabolism
  • Image Processing, Computer-Assisted
  • Lymph Nodes / cytology
  • Lymph Nodes / immunology
  • Lymph Nodes / metabolism
  • Mice
  • Mice, Transgenic
  • Microscopy* / methods
  • Plasma Cells / cytology*
  • Plasma Cells / immunology*
  • Plasma Cells / metabolism
  • Time Factors