Bibliografías temáticas / Membrane lysosomale

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Literatura académica sobre el tema "Membrane lysosomale"

Autor: Grafiati
Publicado: 1 de febrero de 2025
Última modificación: 31 de julio de 2025

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Artículos de revistas sobre el tema "Membrane lysosomale"

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Li, Yuan, Baohui Chen, Wei Zou, et al. "The lysosomal membrane protein SCAV-3 maintains lysosome integrity and adult longevity." Journal of Cell Biology 215, no. 2 (2016): 167–85. http://dx.doi.org/10.1083/jcb.201602090.

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Lysosomes degrade macromolecules and recycle metabolites as well as being involved in diverse processes that regulate cellular homeostasis. The lysosome is limited by a single phospholipid bilayer that forms a barrier to separate the potent luminal hydrolases from other cellular constituents, thus protecting the latter from unwanted degradation. The mechanisms that maintain lysosomal membrane integrity remain unknown. Here, we identified SCAV-3, the Caenorhabditis elegans homologue of human LIMP-2, as a key regulator of lysosome integrity, motility, and dynamics. Loss of scav-3 caused rupture
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Stark, Michal, Tomás F. D. Silva, Guy Levin, Miguel Machuqueiro, and Yehuda G. Assaraf. "The Lysosomotropic Activity of Hydrophobic Weak Base Drugs is Mediated via Their Intercalation into the Lysosomal Membrane." Cells 9, no. 5 (2020): 1082. http://dx.doi.org/10.3390/cells9051082.

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Lipophilic weak base therapeutic agents, termed lysosomotropic drugs (LDs), undergo marked sequestration and concentration within lysosomes, hence altering lysosomal functions. This lysosomal drug entrapment has been described as luminal drug compartmentalization. Consistent with our recent finding that LDs inflict a pH-dependent membrane fluidization, we herein demonstrate that LDs undergo intercalation and concentration within lysosomal membranes. The latter was revealed experimentally and computationally by (a) confocal microscopy of fluorescent compounds and drugs within lysosomal membrane
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Mangalanathan, Malathi, Tamiloli Devendhiran, Saraswathi Uthamaramasamy, et al. "Isolation and characterization of mitochondria and lysosome from isoproterenol induced cardiotoxic rats." South Asian Journal of Engineering and Technology 8, no. 1 (2019): 12–18. http://dx.doi.org/10.26524/sajet190804.

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Mitochondrial and lysosomal membranes are prominent membranes of cardiac cells and are the factors that determine membrane function in myocardial ischemia. In this study, isolation of mitochondria and lysosome from heart tissue under the control, isoproterenol (ISO) (8.5mg/100g) induced cardiotoxic rats and oral pretreatment with Z. armatum fruit (200, 400mg/kg body weight) treated rats. Further characterization of marker enzymes was done. A decreased in the activity of all the mitochondrial and lysosomal marker enzymes in ISO administered cardiotoxic rats when compared to control rats which i
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Boonen, Marielle, Isabelle Hamer, Muriel Boussac, et al. "Intracellular localization of p40, a protein identified in a preparation of lysosomal membranes." Biochemical Journal 395, no. 1 (2006): 39–47. http://dx.doi.org/10.1042/bj20051647.

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Unlike lysosomal soluble proteins, few lysosomal membrane proteins have been identified. Rat liver lysosomes were purified by centrifugation on a Nycodenz density gradient. The most hydrophobic proteins were extracted from the lysosome membrane preparation and were identified by MS. We focused our attention on a protein of approx. 40 kDa, p40, which contains seven to ten putative transmembrane domains and four lysosomal consensus sorting motifs in its sequence. Knowing that preparations of lysosomes obtained by centrifugation always contain contaminant membranes, we combined biochemical and mo
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Tang, Tuoxian, Boshuo Jian, and Zhenjiang Liu. "Transmembrane Protein 175, a Lysosomal Ion Channel Related to Parkinson’s Disease." Biomolecules 13, no. 5 (2023): 802. http://dx.doi.org/10.3390/biom13050802.

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Lysosomes are membrane-bound organelles with an acidic lumen and are traditionally characterized as a recycling center in cells. Lysosomal ion channels are integral membrane proteins that form pores in lysosomal membranes and allow the influx and efflux of essential ions. Transmembrane protein 175 (TMEM175) is a unique lysosomal potassium channel that shares little sequence similarity with other potassium channels. It is found in bacteria, archaea, and animals. The prokaryotic TMEM175 consists of one six-transmembrane domain that adopts a tetrameric architecture, while the mammalian TMEM175 is
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Feng, Xinghua, Zhuangzhuang Zhao, Qian Li, and Zhiyong Tan. "Lysosomal Potassium Channels: Potential Roles in Lysosomal Function and Neurodegenerative Diseases." CNS & Neurological Disorders - Drug Targets 17, no. 4 (2018): 261–66. http://dx.doi.org/10.2174/1871527317666180202110717.

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Background & Objective: The lysosome is a membrane-enclosed organelle widely found in every eukaryotic cell. It has been deemed as the stomach of the cells. Recent studies revealed that it also functions as an intracellular calcium store and is a platform for nutrient-dependent signal transduction. Similar with the plasma membrane, the lysosome membrane is furnished with various proteins, including pumps, ion channels and transporters. So far, two types of lysosomal potassium channels have been identified: large-conductance and Ca2+-activated potassium channel (BK) and TMEM175. TMEM175 has
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Israels, S. J., E. M. McMillan, C. Robertson, S. Singhroy, and A. McNicol. "The Lysosomal Granule Membrane Protein, Lamp-2, Is also Present in Platelet Dense Granule Membranes." Thrombosis and Haemostasis 75, no. 04 (1996): 623–29. http://dx.doi.org/10.1055/s-0038-1650333.

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SummaryLysosomal Associated Membrane Protein-2 (LAMP-2) is an inherent component of lysosomal granule membranes in diverse cell types, including platelets. We examined platelets for evidence of LAMP-2 in dense granule membranes as CD63 has previously been shown to be present in both lysosomal and dense granule membranes. Immunological techniques were used to examine the localization of LAMP-2 in control platelets and those from an individual with Hermansky-Pudlak syndrome (HPS), a condition characterised by platelet dense granule deficiency. Immunoblotting studies demonstrated that LAMP-2 was
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Wang, Wuyang, Xiaoli Zhang, Qiong Gao, et al. "A voltage-dependent K+ channel in the lysosome is required for refilling lysosomal Ca2+ stores." Journal of Cell Biology 216, no. 6 (2017): 1715–30. http://dx.doi.org/10.1083/jcb.201612123.

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The resting membrane potential (Δψ) of the cell is negative on the cytosolic side and determined primarily by the plasma membrane’s selective permeability to K+. We show that lysosomal Δψ is set by lysosomal membrane permeabilities to Na+ and H+, but not K+, and is positive on the cytosolic side. An increase in juxta-lysosomal Ca2+ rapidly reversed lysosomal Δψ by activating a large voltage-dependent and K+-selective conductance (LysoKVCa). LysoKVCa is encoded molecularly by SLO1 proteins known for forming plasma membrane BK channels. Opening of single LysoKVCa channels is sufficient to cause
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Chen, J. W., T. L. Murphy, M. C. Willingham, I. Pastan, and J. T. August. "Identification of two lysosomal membrane glycoproteins." Journal of Cell Biology 101, no. 1 (1985): 85–95. http://dx.doi.org/10.1083/jcb.101.1.85.

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Two murine lysosome-associated membrane proteins, LAMP-1 of 105,000-115,000 D and LAMP-2 of 100,000-110,000 D, have been identified by monoclonal antibodies that bind specifically to lysosomal membranes. Both glycoproteins were distinguished as integral membrane components solubilized by detergent solutions but not by various chaotropic agents. The lysosome localization was demonstrated by indirect immunofluorescent staining, co-localization of the antigen to sites of acridine orange uptake, and immunoelectron microscopy. Antibody binding was predominantly located at the limiting lysosomal mem
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Wilson, J. M., J. A. Whitney, and M. R. Neutra. "Biogenesis of the apical endosome-lysosome complex during differentiation of absorptive epithelial cells in rat ileum." Journal of Cell Science 100, no. 1 (1991): 133–43. http://dx.doi.org/10.1242/jcs.100.1.133.

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Absorptive cells of the neonatal rat ileum have an elaborate apical endocytic complex consisting of tubular and vesicular endosomes, multivesicular bodies (MVB), and a giant lysosomal vacuole. This system develops rapidly over the last 3 days (20–22) of gestation. We followed the assembly of this complex by ultrastructural analysis and immunocytochemistry using antigenic markers for microvilli, endosomal tubules and lysosomal membranes. At 19 days gestation, low levels of lactase appeared on microvilli but specialized apical endosomal tubules and lysosomes were absent. At 20 days, expression o
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Tesis sobre el tema "Membrane lysosomale"

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Jamal, Layal. "Structural and functional characterization of the lysosomal amino acid transporter PQLC2." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASL129.

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PQLC2, qui signifie protéine conte- nant des répétitions de boucle proline-glutamine 2, appartient à une famille de protéines de transport membranaires caractérisées par une topologie membranaire à sept hélices et deux motifs proline-glutamine. PQLC2 est localisé dans la membrane lysosomale des cellules mammifères, et des études utilisant du PQLC2 recombinant exprimé dans des ovocytes de Xenopus ont démontré que PQLC2 est un uniporteur qui transporte spécifiquement des acides aminés cationiques. Cependant, sa structure atomique en 3D n’a pas encore été déterminée. En plus de son rôle de transp
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SAMARANI, MAURA. "CELL DAMAGE INDUCED BY LYSOSOMAL IMPAIRMENT: STUDY OF THE ROLE OF PLASMA MEMBRANE SPHINGOLIPIDS." Doctoral thesis, Università degli Studi di Milano, 2017. http://hdl.handle.net/2434/482301.

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Lysosomes are the principal site of the catabolism of sphingolipids, a class of bioactive lipids mainly associated with the external leaflet of cell plasma membrane. Several lines of evidence support a direct correlation between modifications in sphingolipid pattern and the activation of specific signaling pathways, including apoptosis and autophagy. Loss-of-function mutations in genes coding for lysosomal enzymes involved in sphingolipid catabolism result in severe clinical manifestations called sphingolipidoses. These pathologies belong to the group of Lysosomal Storage Diseases and are char
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Schröder, Bernd. "Proteomanalyse der humanen lysosomalen Membran /." Marburg : Görich & Weiershäuser, 2007. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=016450683&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.

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Johansson, Ann-Charlotte. "Lysosomal membrane permeabilization : a cellular suicide strategy /." Linköping : Department of Clinical and Experimental Medicine, Linköping University, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-11614.

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Johansson, Ann-Charlotte. "Lysosomal Membrane Permeabilization : A Cellular Suicide Stragegy." Doctoral thesis, Linköpings universitet, Experimentell patologi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-11614.

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In the last decade, a tremendous gain in knowledge concerning the molecular events of apoptosis signaling and execution has been achieved. The aim of this thesis was to clarify the role of lysosomal membrane permeabilization and lysosomal proteases, cathepsins, in signaling for apoptosis. We identified cathepsin D as an important factor in staurosporine-induced human fibroblast cell death. After release to the cytosol, cathepsin D promoted mitochondrial release of cytochrome c by proteolytic activation of Bid. Cathepsin D-mediated cleavage of Bid generated two fragments with the apparent molec
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Schneede, Alexander [Verfasser]. "Leben ohne LAMPs : die Folgen des Fehlens der lysosomal assoziierten Membran Proteine LAMP-1 und LAMP-2 auf endosomale, lysosomale Prozesse / Alexander Schneede." Kiel : Universitätsbibliothek Kiel, 2009. http://d-nb.info/1019811161/34.

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Iveson, Graeme Paul. "Passive diffusion across the lysosome membrane." Thesis, Keele University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315231.

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Appelqvist, Hanna. "Lysosomal Membrande Stability and Cathepsins in Cell Death." Doctoral thesis, Linköpings universitet, Experimentell patologi, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-85008.

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Lysosomes are acidic organelles that are critically involved in a number of physiological processes, including macromolecule degradation, endocytosis, autophagy, exocytosis and cholesterol homeostasis. Several pathological conditions, such as cancer, neurodegenerative disorders and lysosomal storage diseases, involve lysosomal disturbances, indicating the importance of the organelle for correct cellular function. The aim of this thesis was to investigate the role of lysosomes in cell death signaling. Previous studies have shown that permeabilization of the lysosomal membrane and release of hyd
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Lachuer, Hugo. "Role of membrane tension in the spatial regulation of lysosomal exocytosis." Electronic Thesis or Diss., Université Paris sciences et lettres, 2022. http://www.theses.fr/2022UPSLS026.

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L'exocytose lysosomale est impliquée dans plusieurs processus cellulaires, mais sa régulation spatio-temporelle est encore peu connue. En utilisant la microscopie de fluorescence à réflexion totale (TIRFM) et des outils de statistiques spatiales, nous avons observé que l’exocytose aléatoire n’était pas distribuée aléatoirement sur la face ventrale de la membrane plasmique de cellules RPE1, mais organisée en agglomérats sur plusieurs échelles de tailles. Même si le taux d’exocytose est régulé par le cytosquelette d’actine, des perturbations de l’actine ou des microtubules par des drogues n’altè
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Apfeldorfer, Coralie. "Lysosome biogenesis during osteoclastogenesis." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2006. http://nbn-resolving.de/urn:nbn:de:swb:14-1164801444532-19433.

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Lysosomes are acidic, hydrolase-rich vesicles capable of degrading most biological macromolecules. During the past several decades, much has been learned about different aspects of lysosome biogenesis. The selective phosphorylation of mannose residues on lysosomal enzymes, in conjunction with specific receptors for the mannose-6-phosphate recognition marker, has been found to be largely responsible for the targeting of newly synthesized lysosomal enzymes to lyzosomes. It is known that lysosomes receive input from both the endocytotic and biosynthetic pathways. Nevertheless the exact molecular
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Libros sobre el tema "Membrane lysosomale"

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Johansson, Ann-Charlotte. Lysosomal membrane permeabilization: A cellular suicide strategy. Department of Clinical and Experimental Medicine, Linköping University, 2008.

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A, Azzi, Drahota Z, Papa S, Unesco, and International Biomedical Institute, eds. Molecular basis of membrane-associated diseases. Springer-Verlag, 1989.

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Azzi, Angelo, Sergio Papa, and Zdenek Drahota. Molecular Basis of Membrane-Associated Diseases. Springer, 2011.

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Azzi, Angelo, Sergio Papa, and Zdenek Drahota. Molecular Basis of Membrane-Associated Diseases. Springer London, Limited, 2012.

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Capítulos de libros sobre el tema "Membrane lysosomale"

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Schwake, Michael, and Paul Saftig. "Lysosomal Membrane Defects." In Lysosomal Storage Disorders. John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118514672.ch17.

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Kuma, Akiko, and Tamotsu Yoshimori. "Pathways to Repair or Remove Lysosomes Damaged by Extracellular Fine Particles." In Extracellular Fine Particles. Springer Nature Singapore, 2025. https://doi.org/10.1007/978-981-97-7067-0_13.

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Abstract Exogenous and endogenous fine particles such as environmental materials (e.g., silica, asbestos, alum), toxic protein aggregates (e.g., α-synuclein, amyloid-β), and endogenous crystals (e.g., cholesterol crystals, uric acid crystals) are internalized into the cell by the endocytic pathway or phagocytosis. Because lysosomes are the terminal compartments of these pathways, lysosomes are known to be damaged by exocytosed extracellular fine particles. Lysosomal membrane damage allows the leakage of the lysosomal contents such as cathepsins, H+, Ca2+, and iron into the cytosol, which is ha
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Coninck, S. Wattiaux-De, M. M. Gonze, L. De Waele, et al. "LGP10D10, a Lysosomal Membrane Protein." In Endocytosis. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84295-5_29.

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Fukuda, Minoru. "Biogenesis of the Lysosomal Membrane." In Subcellular Biochemistry. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2401-4_7.

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Erickson, Ann H., Gail F. Mclntyre, Gene D. Godbold, and Richard L. Chapman. "A New Receptor for Lysosomal Proenzymes." In Molecular Mechanisms of Membrane Traffic. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-662-02928-2_73.

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Harikumar, P., and John P. Reeves. "The Lysosomal Proton Pump." In New Insights into Cell and Membrane Transport Processes. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5062-0_4.

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Williamson, Chad D., Carlos M. Guardia, Raffaella De Pace, Juan S. Bonifacino, and Amra Saric. "Measurement of Lysosome Positioning by Shell Analysis and Line Scan." In Membrane Trafficking. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2209-4_19.

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Verheijen, Frans W., and Grazia M. S. Mancini. "Lysosomal sialic acid transporter sialin (SLC17A5): sialic acid storage disease (SASD)." In Membrane Transporter Diseases. Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-9023-5_15.

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Repnik, Urška, and Boris Turk. "Lysosomal Membrane Permeabilization in Cell Death." In Lysosomes: Biology, Diseases, and Therapeutics. John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781118978320.ch8.

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Giraldo, Ana Maria Vilamill, Karin Öllinger, and Vesa Loitto. "Microscopic Analysis of Lysosomal Membrane Permeabilization." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6934-0_5.

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Actas de conferencias sobre el tema "Membrane lysosomale"

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Silva, Jordan Da, Celia Bienassis, and Sebastien Paris. "1092 Induction of lysosomal membrane permeabilization by radiotherapy-activated NBTXR3 nanoparticles." In SITC 38th Annual Meeting (SITC 2023) Abstracts. BMJ Publishing Group Ltd, 2023. http://dx.doi.org/10.1136/jitc-2023-sitc2023.1092.

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Dalzell, Danielle R., Caleb C. Roth, Joshua A. Bernhard, Jason A. Payne, Gerald J. Wilmink, and Bennett L. Ibey. "Lysosomal exocytosis in response to subtle membrane damage following nanosecond pulse exposure." In SPIE BiOS, edited by Thomas P. Ryan. SPIE, 2011. http://dx.doi.org/10.1117/12.874358.

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Mena, Salvador, Maria Rodriguez, Miguel Asensi, Jose M. Estrela, and Angel Ortega. "Abstract 4219: Lysosomal membrane permeabilization, a novel anticancer mechanism induced by pterostilbene." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-4219.

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Wiedmer, Tabea, Rasmus M. Frank, Mario P. Tschan, Aurel Perren, and Ilaria Marinoni. "Abstract 3159: Lysosomal membrane permeabilization as potential mediator of resistance in pancreatic neuroendocrine tumors." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3159.

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Purdon, A. D., and J. B. Smith. "ISOLATION OF A SOLUBLE PHOSPHOLIPASE A2 FROM HUMAN PLATELETS ACTIVE AGAINST 1-ACYL-2-ARACHIDONOYL GLYCEROPHOSPHOCHOLINE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644628.

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Previously, we have shown that 1-acyl-2-arachidonoyl glycero-phosphocholine (GPC) is the main source of arachidonic acid in thrombin-stimulated (5 U/ml) human platelets. Thus 1-acyl-2-3H-arachidonoyl GPC was dispersed in Tris buffer, 0.01 M, pH 7.5, 0.01 M CaCl2 for use a substrate for the assay of phospholipase A2 activity in human platelets. The released 3H-arachidonate(AA) was isolated by thin layer chromatography following Bligh and Dyer extraction of the enzyme-substrate incubate. Phospholipase A2 (PLA2) specific for this phospholipid was thought to be membrane bound and of low activity w
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Jia, Caixia, Jianmin Shi, Tao Han, Ping Cai, Alfred C. H. Yu, and Peng Qin. "Lysosome Exocytosis Involved in the Resealing of the Perforated Membrane by Acoustic Cavitation." In 2018 IEEE International Ultrasonics Symposium (IUS). IEEE, 2018. http://dx.doi.org/10.1109/ultsym.2018.8579659.

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Circu, Magdalena, James Cardelli, Glenn Mills, Martin Barr, and Hazem E. El-Osta. "Abstract 3511: Chloroquine-induced lysosomal membrane permeabilization restores sensitivity to cisplatin in refractory lung cancer cells." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-3511.

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Alvi, Mohammed, Rachel Nicoletto, Bayan A. Eshmawi, and Clyde M. Ofner. "Abstract 2091: Lysosomal targeting of doxorubicin induces different membrane permeabilization and cytotoxicity in two breast cancer cell lines." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-2091.

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Alvi, Mohammed, Rachel Nicoletto, Bayan A. Eshmawi, and Clyde M. Ofner. "Abstract 2091: Lysosomal targeting of doxorubicin induces different membrane permeabilization and cytotoxicity in two breast cancer cell lines." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-2091.

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Thirusangu, Prabhu, Christopher L. Pathoulas, Upasana Ray, et al. "Abstract 1937: Quinacrine-induced autophagy in ovarian cancer triggers cathepsin-L mediated lysosomal/mitochondrial membrane permeabilization and cell death." In Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-1937.

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