Parenchymal trafficking of pleural mesothelial cells in idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is characterised by myofibroblast proliferation leading to architectural destruction. Neither the origin nor the continued proliferation of myofibroblasts is well understood. Explanted human IPF lungs were stained by immunohistochemistry for calretinin, a marker o...

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Veröffentlicht in:	The European respiratory journal 2012-01, Vol.39 (1), p.133-140
Hauptverfasser:	MUBARAK, K. K, MONTES-WORBOYS, A, NATHAN, S. D, ANTONY, V. B, REGEV, D, NASREEN, N, MOHAMMED, K. A, FARUQI, I, HENSEL, E, BAZ, M. A, AKINDIPE, O. A, FERNANDEZ-BUSSY, S
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Animals Biological and medical sciences Calbindin 2 Cell Nucleus - metabolism Child Cystic Fibrosis - metabolism Epithelial-Mesenchymal Transition Epithelium - pathology Female GPI-Linked Proteins - blood Humans Idiopathic Pulmonary Fibrosis - physiopathology Immunohistochemistry - methods Lung - metabolism Male Medical sciences Mice Mice, Inbred C57BL Middle Aged Myofibroblasts - cytology Pleura - metabolism Pneumology Pulmonary Disease, Chronic Obstructive - metabolism Respiratory system : syndromes and miscellaneous diseases S100 Calcium Binding Protein G - blood
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