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DOI 10.1369/0022155412456380

Медицинская библиотека · The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2012

Biglycan: a multivalent proteoglycan providing structure and signals.

Nastase Madalina V, Young Marian F, Schaefer Liliana

СтатьяResearch Support, N.I.H., IntramuralПоддержка исследования: вне правительства СШАОбзорПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Nastase Madalina V, Young Marian F, Schaefer Liliana. Biglycan: a multivalent proteoglycan providing structure and signals.. The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society. 2012. DOI: 10.1369/0022155412456380.

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