| First Author | Lai L | Year | 2021 |
| Journal | Int J Biol Sci | Volume | 17 |
| Issue | 3 | Pages | 742-755 |
| PubMed ID | 33767585 | Mgi Jnum | J:324451 |
| Mgi Id | MGI:6753486 | Doi | 10.7150/ijbs.56424 |
| Citation | Lai L, et al. (2021) Bovine serum albumin aggravates macrophage M1 activation and kidney injury in heterozygous Klotho-deficient mice via the gut microbiota-immune axis. Int J Biol Sci 17(3):742-755 |
| abstractText | Klotho expression abnormalities induces kidney injury and chronic kidney disease, however, the underlying mechanism remains unclear. Here, Klotho(+/-) mice and wild-type mice were treated with low-dose bovine serum albumin (BSA). Pathological examination demonstrated that the area of glomerular collagen deposition and fibrosis in BSA-Kl(-/+) mice was significantly larger than that in BSA-WT mice. The serum levels of superoxide dismutase, malondialdehyde, creatinine, and urea in BSA-Kl(-/+) mice were significantly increased. Sequencing of gut microbiota 16S rRNA v3-v4 region indicated that BSA-Kl(-/+) mice showed a significantly higher relative abundance of the genera Dubosiella, Akkermansia, Alloprevotella, and Lachnospiraceae and a significantly lower relative abundance of the genera Allobaculum and Muribaculaceae than BSA-WT mice. KEGG analysis revealed that the metabolic pathways of signal transduction, xenobiotic biodegradation and metabolism, and lipid metabolism increased significantly in BSA-Kl(-/+) mice. Flow cytometry showed that the proportion of CD68(+)/CD11b(+) cells in the peripheral blood was significantly higher in BSA-KL(-/+) mice than that in BSA-WT mice. qPCR and western blot suggested that Klotho and Nrf2 expression in MPhi1 cells of BSA-KL(-/+) mice was significantly decreased. Thus, the findings suggest during the immune activation and chronic inflammation induced by the gut microbiota imbalance in Klotho-deficient mice treated to BSA, disrupted expression of proteins in the Nrf2/NF-kappaB signaling pathway in monocyte-derived macrophage M1 cells leads to the aggravation of inflammation and kidney injury. |
