4.2 Article

Biglycan: A Multivalent Proteoglycan Providing Structure and Signals

Journal

JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
Volume 60, Issue 12, Pages 963-975

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1369/0022155412456380

Keywords

extracellular matrix; proteoglycan; Toll-like receptor; inflammasome; TGF beta; inflammation; bone; skeletal muscle; Duchenne's muscular dystrophy; sepsis; Wnt

Categories

Funding

  1. German Research Council [SFB 815]
  2. SCHA [1082/2-1]
  3. Excellence Cluster ECCPS
  4. Division of Intramural Research, NIDCR of the Intramural Program NIH, Department of Health and Human Services
  5. [GRK1172]

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Research over the past few years has provided fascinating results indicating that biglycan, besides being a ubiquitous structural component of the extracellular matrix (ECM), may act as a signaling molecule. Proteolytically released from the ECM, biglycan acts as a danger signal signifying tissue stress or injury. As a ligand of innate immunity receptors and activator of the inflammasome, biglycan stimulates multifunctional proinflammatory signaling linking the innate to the adaptive immune response. By clustering several types of receptors on the cell surface and orchestrating their downstream signaling events, biglycan is capable to autonomously trigger sterile inflammation and to potentiate the inflammatory response to microbial invasion. Besides operating in a broad biological context, biglycan also displays tissue-specific affinities to certain receptors and structural components, thereby playing a crucial role in bone formation, muscle integrity, and synapse stability at the neuromuscular junction. This review attempts to provide a concise summary of recent data regarding the involvement of biglycan in the regulation of inflammation and the musculoskeletal system, pointing out both a signaling and a structural role for this proteoglycan. The potential of biglycan as a novel therapeutic target or agent for the treatment of inflammatory diseases and skeletal muscular dystrophies is also addressed. (J Histochem Cytochem 60:963-975, 2012)

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