4.7 Article

Developmental stages of tertiary lymphoid tissue reflect local injury and inflammation in mouse and human kidneys

期刊

KIDNEY INTERNATIONAL
卷 98, 期 2, 页码 448-463

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2020.02.023

关键词

follicular dendritic cell; renal aging; renal inflammation; tertiary lymphoid tissues

资金

  1. Japan Agency for Medical Research and Development (AMED) [JP18gm5010002, JP18gm0610011]
  2. TMK Project
  3. Ministry of Education, Culture, Sports, Science and Technology of Japan [26293202, 17H04187, 17H05642]
  4. Japan Society for the Promotion of Science
  5. AMED
  6. Uehara Memorial Foundation
  7. Takeda Science Foundation
  8. Sumitomo Foundation
  9. German Research Foundation [SFB TRR 57, SFB TRR 219, BO3755/3-1, BO3755/6-1]
  10. German Ministry of Education and Research [STOP-FSGS-01GM1518A]
  11. World Premier International Research Center Initiative, Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan
  12. [AMEDCREST19gm1210009]
  13. Grants-in-Aid for Scientific Research [26293202, 17H04187, 17H05642] Funding Source: KAKEN

向作者/读者索取更多资源

Tertiary lymphoid tissues (TLTs) are inducible ectopic lymphoid tissues in chronic inflammatory states and function as sites of priming local immune responses. We previously demonstrated that aged but not young mice exhibited multiple TLTs after acute kidney injury and that TLTs were also detected in human aged and diseased kidneys. However, the forms of progression and the implication for kidney injury remain unclear. To clarify this we analyzed surgically resected kidneys from aged patients with or without chronic kidney disease as well as kidneys resected for pyelonephritis, and classified TLTs into three distinct developmental stages based on the presence of follicular dendritic cells and germinal centers. In injury-induced murine TLT models, the stages advanced with the extent of kidney injury, and decreased with dexamethasone accompanied with improvement of renal function, fibrosis and inflammation. Kidneys from aged patients with chronic kidney disease consistently exhibited more frequent and advanced stages of TLTs than those without chronic kidney disease. Kidneys of patients with pyelonephritis exhibited more frequent TLTs with more advanced stages than aged kidneys. Additionally, TLTs in both cohorts shared similar locations and components, suggesting that TLT formation may not be a disease-specific phenomenon but rather a common pathological process. Thus, our findings provide the insights into biological features of TLT in the kidney and implicate TLT stage as a potential marker reflecting local injury and inflammation.

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