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Proteoglycans as Immunomodulators of the Innate Immune Response to Lung Infection.
Kang, Inkyung; Chang, Mary Y; Wight, Thomas N; Frevert, Charles W.
Affiliation
  • Kang I; Matrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington.
  • Chang MY; Comparative Pathology Program, Department of Comparative Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Wight TN; Matrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington.
  • Frevert CW; Center for Lung Biology, Division of Pulmonary/Critical Care Medicine, University of Washington School of Medicine, Seattle, Washington.
J Histochem Cytochem ; 66(4): 241-259, 2018 04.
Article in En | MEDLINE | ID: mdl-29328866
ABSTRACT
Proteoglycans (PGs) are complex, multifaceted molecules that participate in diverse interactions vital for physiological and pathological processes. As structural components, they provide a scaffold for cells and structural organization that helps define tissue architecture. Through interactions with water, PGs enable molecular and cellular movement through tissues. Through selective ionic interactions with growth factors, chemokines, cytokines, and proteases, PGs facilitate the ability of these soluble ligands to regulate intracellular signaling events and to influence the inflammatory response. In addition, recent findings now demonstrate that PGs can activate danger-associated molecular patterns (DAMPs) and other signaling pathways to influence production of many of these soluble ligands, indicating a more direct role for PGs in influencing the immune response and tissue inflammation. This review will focus on PGs that are selectively expressed during lung inflammation and will examine the novel emerging concept of PGs as immunomodulatory regulators of the innate immune responses in lungs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia / Proteoglycans / Immunity, Innate / Lung Limits: Animals / Humans Language: En Journal: J Histochem Cytochem Journal subject: HISTOCITOQUIMICA Year: 2018 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia / Proteoglycans / Immunity, Innate / Lung Limits: Animals / Humans Language: En Journal: J Histochem Cytochem Journal subject: HISTOCITOQUIMICA Year: 2018 Type: Article