[Immunosenescence: The Forefront of Infection and Trophic Control]

Yakugaku Zasshi. 2020;140(3):391-393. doi: 10.1248/yakushi.19-00193-3.
[Article in Japanese]

Abstract

Recently, aging is becoming an important social problem in many developed countries including Japan. It is socially and universally important to unveil the impact of aging and extend healthy life expectancy. Here we show our recent finding that dedicator of cytokinesis 11 (DOCK11, also known as Zizimin2) may be involved in immunosenescence of B cells. DOCK11 was identified as a guanine nucleotide exchange factor for a small GTPase called cell division cycle 42. Expression of DOCK11 is restricted to lymphoid tissues, and becomes downregulated with age. Thus we examined the involvement of DOCK11 in immunosenescence of B-1a B cells as an example. B-1a cells are the main source of antibodies at steady state, and function as the first line of defense against infection. Although DOCK11 was expressed by B-1a cells, the expression levels declined with age. Furthermore, production of anti-pneumococcal immunoglobulin M antibodies was suppressed in aged mice, and was recovered by adoptive transfer with B-1a cells in a DOCK11-dependent manner. Thus DOCK11 may be involved in immunosenescence of B-1a cells.

Keywords: B-1a B cell; dedicator of cytokinesis 11; immunosenescence.

Publication types

  • Review

MeSH terms

  • Aging / immunology*
  • Animals
  • B-Lymphocytes / immunology
  • Cytokinesis / immunology
  • Gene Expression
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / immunology
  • Guanine Nucleotide Exchange Factors / metabolism
  • Humans
  • Immunoglobulin M
  • Immunosenescence*
  • Mice
  • Nutritional Status
  • Streptococcus pneumoniae / immunology

Substances

  • Dock11 protein, mouse
  • Guanine Nucleotide Exchange Factors
  • Immunoglobulin M