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Relationship between Cellular Microenvironment and Idiopathic Pulmonary Fibrosis / 中国医学科学院学报
Acta Academiae Medicinae Sinicae ; (6): 410-416, 2020.
Article in Chinese | WPRIM | ID: wpr-826347
ABSTRACT
Idiopathic pulmonary fibrosis(IPF)is a progressive lung disease characterized by pulmonary interstitial fibrosis and pulmonary dysfunction.Cell microenvironment is mainly composed of cell components,extracellular matrix,extracellular regulators,and liquid substances.Changes in microenvironment components are closely related to IPF.This article elaborates the roles of cell microenvironments including cytokines,mesenchymal cells,extracellular matrix,and unfolded proteins in the pathogenesis of IPF.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Extracellular Matrix / Idiopathic Pulmonary Fibrosis / Cellular Microenvironment / Lung Limits: Humans Language: Chinese Journal: Acta Academiae Medicinae Sinicae Year: 2020 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Extracellular Matrix / Idiopathic Pulmonary Fibrosis / Cellular Microenvironment / Lung Limits: Humans Language: Chinese Journal: Acta Academiae Medicinae Sinicae Year: 2020 Type: Article