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Published on: October 26, 2020
Protein level expression of Toll-like receptors 2, 4 and 9 in renal disease
Stephen Batsford1, Ursula Duermueller, Christian Seemayer
1Institute for Pathology, University Hospital Basel, Basel, Switzerland. stephen.batsford@uniklinik-freiburg.de
Background:
Toll-like receptors (TLR) recognize a variety of ligands, including pathogen-associated molecular patterns and link innate and adaptive immunity. Individual receptors can be up-regulated during infection and inflammation. We examined the expression of selected TLRs at the protein level in various types of renal disease.
Methods:
Frozen sections of renal biopsies were stained with monoclonal antibodies to TLR-2, -4 and -9.
Results:
Up-regulation of the three TLRs studied was seen, although the extent was modest. TLR-2- and -4-positive cells belonged to the population of infiltrating inflammatory cells; only in the case of TLR-9 were intrinsic glomerular cells positive in polyoma virus infection and haemolytic uraemic syndrome (HUS).
Conclusions:
Evidence for the involvement of the three TLRs tested in a variety of human renal diseases was found. These findings add to our understanding of the role of the innate immune system in kidney disease.
Insights
This study found increased expression of Toll-like receptors (TLRs) 2, 4, and 9 in various kidney diseases. These findings highlight the role of the innate immune system in renal pathology.
Area of Science:
- Immunology
- Nephrology
- Molecular Biology
Background:
- Toll-like receptors (TLRs) are crucial for innate immunity, recognizing pathogen-associated molecular patterns and bridging innate and adaptive immunity.
- TLR expression can increase during infection and inflammation.
- This study investigates the protein expression of selected TLRs in different types of renal disease.
Purpose of the Study:
- To examine the protein expression levels of Toll-like receptors (TLR)-2, -4, and -9 in various human renal diseases.
- To determine the cellular localization of these TLRs within kidney tissues.
Main Methods:
- Utilized monoclonal antibodies for immunohistochemical staining of TLR-2, -4, and -9 on frozen renal biopsy sections.
- Analyzed protein expression in different renal disease contexts.
Main Results:
- Modest up-regulation of TLR-2, -4, and -9 was observed across the studied renal diseases.
- TLR-2 and -4 positive cells were primarily infiltrating inflammatory cells.
- Intrinsic glomerular cells showed positivity for TLR-9 in polyoma virus infection and hemolytic uremic syndrome (HUS).
Conclusions:
- The study provides evidence for the involvement of TLR-2, -4, and -9 in human kidney diseases.
- These findings contribute to understanding the innate immune system's role in the pathogenesis of renal conditions.
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