sirt1-null mice develop an autoimmune-like condition

Exp Cell Res. 2008 Oct 1;314(16):3069-74. doi: 10.1016/j.yexcr.2008.07.011. Epub 2008 Jul 23.


The sirt1 gene encodes a protein deacetylase with a broad spectrum of reported substrates. Mice carrying null alleles for sirt1 are viable on outbred genetic backgrounds so we have examined them in detail to identify the biological processes that are dependent on SIRT1. Sera from adult sirt1-null mice contain antibodies that react with nuclear antigens and immune complexes become deposited in the livers and kidneys of these animals. Some of the sirt1-null animals develop a disease resembling diabetes insipidus when they approach 2 years of age although the relationship to the autoimmunity remains unclear. We interpret these observations as consistent with a role for SIRT1 in sustaining normal immune function and in this way delaying the onset of autoimmune disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology*
  • Cells, Cultured
  • Diabetes Insipidus / genetics
  • Diabetes Insipidus / immunology
  • Disease Models, Animal
  • Endotoxins / immunology
  • Female
  • Humans
  • Immunity, Innate
  • Immunoglobulins / immunology
  • Kidney / cytology
  • Kidney / metabolism
  • Liver / cytology
  • Liver / immunology
  • Mice
  • Mice, Knockout
  • Sirtuin 1
  • Sirtuins / genetics
  • Sirtuins / metabolism*
  • Urine


  • Endotoxins
  • Immunoglobulins
  • Sirt1 protein, mouse
  • Sirtuin 1
  • Sirtuins