PLoS ONE (Jan 2022)

The hematopoietic compartment is sufficient for lupus development resulting from the POLB-Y265C mutation.

  • Tania Rahim,
  • Madison A Levinson,
  • Kelly E W Carufe,
  • Matthew Burak,
  • Rithy Meas,
  • Stephen Maher,
  • Alfred L M Bothwell,
  • Naomi Gades,
  • Joann B Sweasy

DOI
https://doi.org/10.1371/journal.pone.0267913
Journal volume & issue
Vol. 17, no. 4
p. e0267913

Abstract

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Systemic lupus erythematosus is a chronic disease characterized by autoantibodies, renal and cutaneous disease, and immune complex formation. Emerging evidence suggests that aberrant DNA repair is an underlying mechanism of lupus development. We previously showed that the POLBY265C/C mutation, which results in development of an aberrant immune repertoire, leads to lupus-like disease in mice. To address whether the hematopoietic compartment is sufficient for lupus development, we transplanted bone marrow cells from POLBY265C/C and POLB+/+ into wild-type congenic mice. Only mice transplanted with the POLBY265C/C bone marrow develop high levels of antinuclear antibodies and renal disease. In conclusion, we show that the hematopoietic compartment harvested from the POLBY265C/C mice is sufficient for development of autoimmune disease.