Journalartikel
Autorenliste: Ahuja, Saket; Knudsen, Lars; Chillappagari, Shashi; Henneke, Ingrid; Ruppert, Clemens; Korfei, Martina; Gochuico, Bernadette R.; Bellusci, Saverio; Seeger, Werner; Ochs, Matthias; Guenther, Andreas; Mahavadi, Poornima
Jahr der Veröffentlichung: 2016
Seiten: L519-L531
Zeitschrift: American Journal of Physiology - Lung Cellular and Molecular Physiology
Bandnummer: 310
Heftnummer: 6
ISSN: 1040-0605
eISSN: 1522-1504
Open Access Status: Green
DOI Link: https://doi.org/10.1152/ajplung.00213.2015
Verlag: American Physiological Society
Abstract:
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, and some patients with HPS develop pulmonary fibrosis, known as HPS-associated interstitial pneumonia (HPSIP). We have previously reported that HPSIP is associated with severe surfactant accumulation, lysosomal stress, and alveolar epithelial cell type II (AECII) apoptosis. Here, we hypothesized that defective autophagy might result in excessive lysosomal stress in HPSIP. Key autophagy proteins, including LC3B lipidation and p62, were increased in HPS1/2 mice lungs. Electron microscopy demonstrated a preferable binding of LC3B to the interior of lamellar bodies in the AECII of HPS1/2 mice, whereas in wild-type mice it was present on the limiting membrane in addition to the interior of the lamellar bodies. Similar observations were noted in human HPS1 lung sections. In vitro knockdown of HPS1 revealed increased LC3B lipidation and p62 accumulation, associated with an increase in proapoptotic caspases. Overexpression of LC3B decreased the HPS1 knock-down-induced p62 accumulation, whereas rapamycin treatment did not show the same effect. We conclude that loss of HPS1 protein results in impaired autophagy that is restored by exogenous LC3B and that defective autophagy might therefore play a critical role in the development and progression of HPSIP.
Zitierstile
Harvard-Zitierstil: Ahuja, S., Knudsen, L., Chillappagari, S., Henneke, I., Ruppert, C., Korfei, M., et al. (2016) MAP1LC3B overexpression protects against Hermansky-Pudlak syndrome type-1-induced defective autophagy in vitro, American Journal of Physiology - Lung Cellular and Molecular Physiology, 310(6), pp. L519-L531. https://doi.org/10.1152/ajplung.00213.2015
APA-Zitierstil: Ahuja, S., Knudsen, L., Chillappagari, S., Henneke, I., Ruppert, C., Korfei, M., Gochuico, B., Bellusci, S., Seeger, W., Ochs, M., Guenther, A., & Mahavadi, P. (2016). MAP1LC3B overexpression protects against Hermansky-Pudlak syndrome type-1-induced defective autophagy in vitro. American Journal of Physiology - Lung Cellular and Molecular Physiology. 310(6), L519-L531. https://doi.org/10.1152/ajplung.00213.2015
Schlagwörter
alveolar epithelial cells; Hermansky-Pudlak syndrome; Hermansky-Pudlak syndrome-associated interstitial pneumonia; INTERSTITIAL PNEUMONIA; lung fibrosis; LYSOSOME-RELATED ORGANELLES; PULMONARY-FIBROSIS; QUALITY-CONTROL