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.
Artigo
em Chinês
| 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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Matriz Extracelular
/
Fibrose Pulmonar Idiopática
/
Microambiente Celular
/
Pulmão
Limite:
Humanos
Idioma:
Chinês
Revista:
Acta Academiae Medicinae Sinicae
Ano de publicação:
2020
Tipo de documento:
Artigo
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