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Journal Article

IL-10 Deficiency Aggravates Renal Inflammation, Fibrosis and Functional Failure in High-Fat Dieted Obese Mice

Dae Hwan Kim; So Young Chun; EunHye Lee; Bomi Kim; BoHyun Yoon; Haejung Gil; Man-Hoon Han; Yun-Sok Ha; Jun Nyung Lee; Tae Gyun Kwon; Bum Soo Kim; Byung Ik Jang
Tissue Engineering and Regenerative Medicine · Vol. 18, Issue 3 · pp. 399-410 · 2021

Abstract

BACKGROUND: High-fat diet-induced obesity is one of the major cause of chronic renal failure. This obesity-related renal failure is mainly caused by inflammatory processes. However, the role of the major anti-inflammatory cytokine interleukin (IL)-10 has not been researched intensively. METHODS: To evaluate the effect of IL-10 deficiency on obesity-related renal failure, the in vivo study was carried with four animal groups; (1) Low-fat dieted C57BL/6 mice, (2) Low-fat dieted IL-10 knockout (KO) mice, (3) High‐fat dieted C57BL/6 mice and (4) High‐fat dieted IL-10 KO mice group. The analysis was carried with blood/urine chemistry, H&E, Oil-Red-O, periodic acid-Schiff and Masson’s trichrome staining immunohistochemistry and real-time PCR methods. RESULTS: At week 12, high‐fat dieted IL-10 KO mice showed 1) severe lipid accumulation in kidneys, cholesterol elevation (in total, serum kidney) and low-density lipoprotein increasion through the SCAP-SREBP2-LDLr pathway; (2) serious histopathologic alterations showing glomerulosclerosis, tubulointerstitial fibrosis and immune cell infiltration; (3) increased pro‐inflammatory cytokines and chemokines expression; (4) enhanced renal fibrosis; and (5) serious functional failure with high serum creatinine and BUN and proteinuria excretion compared to other groups. CONCLUSION: IL-10 deficiency aggravates renal inflammation, fibrosis and functional failure in high-fat dieted obese mice, thus IL-10 therapy could be applied to obesity-related chronic renal failure.

Bibliographic Information

JournalTissue Engineering and Regenerative Medicine
PublisherSpringer
Publication Date2021-06-01
Publication Year2021
Volume18
Issue3
Pages399-410
Document TypeJournal Article
Print ISSN1738-2696
eISSN2212-5469
DOI10.1007/s13770-020-00328-7

Access Information

NARA Access Coverage2012-01-01~Current
Journal Homepagehttps://www.springer.com/journal/13770
Publisher PageOpen Publisher Page
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