B-cell lymphoma/leukaemia 10 and angiotensin II-induced kidney injury

Cardiovasc Res. 2020 Apr 1;116(5):1059-1070. doi: 10.1093/cvr/cvz169.

Abstract

Aims: B-cell lymphoma/leukaemia 10 (Bcl10) is a member of the CARMA-Bcl10-MALT1 signalosome, linking angiotensin (Ang) II, and antigen-dependent immune-cell activation to nuclear factor kappa-B signalling. We showed earlier that Bcl10 plays a role in Ang II-induced cardiac fibrosis and remodelling, independent of blood pressure. We now investigated the role of Bcl10 in Ang II-induced renal damage.

Methods and results: Bcl10 knockout mice (Bcl10 KO) and wild-type (WT) controls were given 1% NaCl in the drinking water and Ang II (1.44 mg/kg/day) for 14 days. Additionally, Bcl10 KO or WT kidneys were transplanted onto WT mice that were challenged by the same protocol for 7 days. Kidneys of Ang II-treated Bcl10 KO mice developed less fibrosis and showed fewer infiltrating cells. Nevertheless, neutrophil gelatinase-associated lipocalin (Ngal) and kidney injury molecule (Kim)1 expression was higher in the kidneys of Ang II-treated Bcl10 KO mice, indicating exacerbated tubular damage. Furthermore, albuminuria was significantly higher in Ang II-treated Bcl10 KO mice accompanied by reduced glomerular nephrin expression and podocyte number. Ang II-treated WT mice transplanted with Bcl10 KO kidney showed more albuminuria and renal Ngal, compared to WT- > WT kidney-transplanted mice, as well as lower podocyte number but similar fibrosis and cell infiltration. Interestingly, mice lacking Bcl10 in the kidney exhibited less Ang II-induced cardiac hypertrophy than controls.

Conclusion: Bcl10 has multi-faceted actions in Ang II-induced renal damage. On the one hand, global Bcl10 deficiency ameliorates renal fibrosis and cell infiltration; on the other hand, lack of renal Bcl10 aggravates albuminuria and podocyte damage. These data suggest that Bcl10 maintains podocyte integrity and renal function.

Keywords: Albuminuria; Angiotensin II; Bcl10; Kidney; Podocyte.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / chemically induced
  • Acute Kidney Injury / genetics
  • Acute Kidney Injury / metabolism*
  • Acute Kidney Injury / pathology
  • Albuminuria / chemically induced
  • Albuminuria / genetics
  • Albuminuria / metabolism
  • Angiotensin II*
  • Animals
  • B-Cell CLL-Lymphoma 10 Protein / deficiency
  • B-Cell CLL-Lymphoma 10 Protein / genetics
  • B-Cell CLL-Lymphoma 10 Protein / metabolism*
  • Cell Movement
  • Disease Models, Animal
  • Fibrosis
  • Hepatitis A Virus Cellular Receptor 1 / metabolism
  • Kidney / metabolism*
  • Kidney / pathology
  • Kidney Transplantation
  • Lipocalin-2 / metabolism
  • Macrophages / metabolism
  • Membrane Proteins / metabolism
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Podocytes / metabolism
  • Podocytes / pathology
  • T-Lymphocyte Subsets / metabolism
  • Time Factors

Substances

  • B-Cell CLL-Lymphoma 10 Protein
  • Bcl10 protein, mouse
  • Havcr1 protein, mouse
  • Hepatitis A Virus Cellular Receptor 1
  • Lipocalin-2
  • Membrane Proteins
  • nephrin
  • Angiotensin II
  • Lcn2 protein, mouse