Microtubule-associated protein tau in murine kidney: role in podocyte architecture

• Published in: Cellular and molecular life sciences : CMLS 2022-02, Vol.79 (2), p.97-97, Article 97
• Main Authors: Vallés-Saiz, Laura, Peinado-Cahuchola, Rocio, Ávila, Jesús, Hernández, Félix
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Animals; Axonal transport; Biochemistry; Biomedical and Life Sciences; Biomedicine; Cell Biology; Central nervous system; Creatinine; Cytoskeleton; Cytoskeleton - metabolism; Green Fluorescent Proteins - genetics; Green Fluorescent Proteins - metabolism; Immunohistochemistry; Kidney - cytology; Kidney - metabolism; Kidney - ultrastructure; Kidney Glomerulus - metabolism; Kidney Glomerulus - ultrastructure; Kidneys; Life Sciences; Metabolism; Mice; Mice, 129 Strain; Mice, Knockout; Mice, Transgenic; Microscopy, Confocal; Microscopy, Immunoelectron; Microtubules - metabolism; Neurodegenerative diseases; Original; Original Article; Podocytes - metabolism; Proteins; Renal cortex; Tau protein; tau Proteins - genetics; tau Proteins - metabolism; Tauopathies - genetics; Tauopathies - metabolism; Transmission electron microscopy; Tubulin
• ISSN: 1420-682X; 1420-9071
• DOI: 10.1007/s00018-021-04106-z

Tau is a cytoskeletal protein that is expressed mainly in neurons and is involved in several cellular processes, such as microtubule stabilization, axonal maintenance, and transport. Altered tau metabolism is related to different tauopathies being the most important Alzheimer’s disease where aberrant hyperphosphorylated and aggregated tau is found in the central nervous system. Here, we have analyzed that function in kidney by using tau knockout mice generated by integrating GFP-encoding cDNA into exon 1 of MAPT (here referred to as Tau GFP/GFP ). IVIS Lumina from PerkinElmer demonstrated GFP expression in the kidney. We then demonstrated by qPCR that the main tau isoform in the kidney is Tau4R. The GFP reporter allowed us to demonstrate that tau is found in the glomeruli of the renal cortex, and specifically in podocytes. This was further confirmed by immunohistochemistry. Tau G FP/GFP mice present a podocyte cytoskeleton more dynamic as they contain higher levels of detyrosinated tubulin than wild-type mice. In addition, transmission electron microscopy studies demonstrated glomerular damage with a decrease in urinary creatinine. Our results prove that tau has an important role in kidney metabolism under normal physiological conditions.