Cytoskeletal features of alveolar myofibroblasts and pericytes in normal human and rat lung
Frozen or paraffin-embedded human and rat lung specimens were stained with antibodies against total actin, alpha-smooth muscle (SM) actin, vimentin, desmin, or gelsolin. Alveolar interstitial myofibroblasts [i.e., contractile interstitial cells (CIC)] were labeled by total actin antibody but not by...
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Published in | The journal of histochemistry and cytochemistry Vol. 40; no. 12; pp. 1955 - 1963 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Los Angeles, CA
Histochemical Soc
01.12.1992
SAGE Publications Histochemical Society |
Subjects | |
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Abstract | Frozen or paraffin-embedded human and rat lung specimens were stained with antibodies against total actin, alpha-smooth muscle (SM) actin, vimentin, desmin, or gelsolin. Alveolar interstitial myofibroblasts [i.e., contractile interstitial cells (CIC)] were labeled by total actin antibody but not by alpha-SM actin antibody. They stained for vimentin and gelsolin and, in rat lungs, most of them for desmin. Pericytes located around venules at the junction of three alveolar septa were always positive for alpha-SM actin and never for desmin. Tissue samples were also immunostained by an alpha-SM actin antibody and studied by electron microscopy. With this technique we confirmed that cells, identified as pericytes on the basis of their location, were intensely labeled by alpha-SM actin antibodies, whereas alveolar myofibroblasts were not. We conclude that in the lung interstitium pericytes and alveolar myofibroblasts have distinct cytoskeletal features, alpha-SM actin antibody staining being a simple method to distinguish between them. Furthermore, it appears that alveolar myofibroblasts have a peculiar pattern of cytoskeletal protein composition which, in the rat, is similar to that previously described for stromal cells in uterine submucosa, liver sinusoids (Ito cells), or the core of intestinal villi. |
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AbstractList | Frozen or paraffin-embedded human and rat lung specimens were stained with antibodies against total actin, alpha-smooth muscle (SM) actin, vimentin, desmin, or gelsolin. Alveolar interstitial myofibroblasts [i.e., contractile interstitial cells (CIC)] were labeled by total actin antibody but not by alpha-SM actin antibody. They stained for vimentin and gelsolin and, in rat lungs, most of them for desmin. Pericytes located around venules at the junction of three alveolar septa were always positive for alpha-SM actin and never for desmin. Tissue samples were also immunostained by an alpha-SM actin antibody and studied by electron microscopy. With this technique we confirmed that cells, identified as pericytes on the basis of their location, were intensely labeled by alpha-SM actin antibodies, whereas alveolar myofibroblasts were not. We conclude that in the lung interstitium pericytes and alveolar myofibroblasts have distinct cytoskeletal features, alpha-SM actin antibody staining being a simple method to distinguish between them. Furthermore, it appears that alveolar myofibroblasts have a peculiar pattern of cytoskeletal protein composition which, in the rat, is similar to that previously described for stromal cells in uterine submucosa, liver sinusoids (Ito cells), or the core of intestinal villi. |
Author | Ribaux, C Kapanci, Y Chaponnier, C Gabbiani, G |
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Keywords | Human Vimentin Pericyte Rat Lung Myofibroblast Rodentia Contractile protein Actins Smooth muscle Respiratory system Desmin Proteins Vertebrata Mammalia Pulmonary alveolus Cytoskeleton Interstitial |
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SubjectTerms | Actins - analysis Actins - immunology Air breathing Animals Antibodies - immunology Arterioles - cytology Biological and medical sciences Calcium-Binding Proteins - analysis Calcium-Binding Proteins - immunology Cytoskeleton - chemistry Cytoskeleton - ultrastructure Desmin - analysis Desmin - immunology Fibroblasts - cytology Fibroblasts - ultrastructure Fluorescent Antibody Technique Fundamental and applied biological sciences. Psychology Gelsolin Humans Lung - cytology Lung - ultrastructure Microfilament Proteins - analysis Microfilament Proteins - immunology Microscopy, Immunoelectron Muscle, Smooth, Vascular - cytology Muscle, Smooth, Vascular - ultrastructure Pulmonary Alveoli - cytology Pulmonary Alveoli - ultrastructure Rats Respiratory system: anatomy, metabolism, gas exchange, ventilatory mechanics, respiratory hemodynamics Vertebrates: respiratory system Vimentin - analysis Vimentin - immunology |
Title | Cytoskeletal features of alveolar myofibroblasts and pericytes in normal human and rat lung |
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