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Small Leucine-Rich Proteoglycans in Renal Inflammation: Two Sides of the Coin.

Abstract
It is now well-established that members of the small leucine-rich proteoglycan (SLRP) family act in their soluble form, released proteolytically from the extracellular matrix (ECM), as danger-associated molecular patterns (DAMPs). By interacting with Toll-like receptors (TLRs) and the inflammasome, the two SLRPs, biglycan and decorin, autonomously trigger sterile inflammation. Recent data indicate that these SLRPs, besides their conventional role as pro-inflammatory DAMPs, additionally trigger anti-inflammatory signaling pathways to tightly control inflammation. This is brought about by selective employment of TLRs, their co-receptors, various adaptor molecules, and through crosstalk between SLRP-, reactive oxygen species (ROS)-, and sphingolipid-signaling. In this review, the complexity of SLRP signaling in immune and kidney resident cells and its relevance for renal inflammation is discussed. We propose that the dichotomy in SLRP signaling (pro- and anti-inflammatory) allows for fine-tuning the inflammatory response, which is decisive for the outcome of inflammatory kidney diseases.
AuthorsMadalina V Nastase, Andrea Janicova, Heiko Roedig, Louise Tzung-Harn Hsieh, Malgorzata Wygrecka, Liliana Schaefer
JournalThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society (J Histochem Cytochem) Vol. 66 Issue 4 Pg. 261-272 (04 2018) ISSN: 1551-5044 [Electronic] United States
PMID29290137 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Biglycan
  • Decorin
  • Inflammasomes
  • Small Leucine-Rich Proteoglycans
  • Transforming Growth Factor beta
Topics
  • Animals
  • Autophagy
  • Biglycan (immunology)
  • Decorin (immunology)
  • Fibrosis
  • Humans
  • Immunity, Innate
  • Inflammasomes (immunology)
  • Inflammation (immunology, pathology)
  • Kidney (cytology, immunology, pathology)
  • Kidney Diseases (immunology, pathology)
  • Signal Transduction
  • Small Leucine-Rich Proteoglycans (immunology)
  • Transforming Growth Factor beta (immunology)

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