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NB 06: From a simple lysosomotropic aSMase inhibitor to tools for elucidating the role of lysosomes in signaling apoptosis and LPS-induced inflammation.
Blaess, Markus; Bibak, Nelly; Claus, Ralf A; Kohl, Matthias; Bonaterra, Gabriel A; Kinscherf, Ralf; Laufer, Stefan; Deigner, Hans-Peter.
Afiliación
  • Blaess M; Furtwangen University, Medical and Life Sciences Faculty, Institute of Precision Medicine, Jakob-Kienzle-Str. 17, D-78054 Villingen-Schwenningen, Germany; Clinic for Anesthesiology and Intensive Care, Jena University Hospital, Am Klinikum 1, D-07747 Jena, Germany.
  • Bibak N; Furtwangen University, Medical and Life Sciences Faculty, Institute of Precision Medicine, Jakob-Kienzle-Str. 17, D-78054 Villingen-Schwenningen, Germany.
  • Claus RA; Clinic for Anesthesiology and Intensive Care, Jena University Hospital, Am Klinikum 1, D-07747 Jena, Germany; Center for Sepsis Control and Care (CSCC), Jena University Hospital, Am Klinikum 1, D-07747 Jena, Germany.
  • Kohl M; Furtwangen University, Medical and Life Sciences Faculty, Institute of Precision Medicine, Jakob-Kienzle-Str. 17, D-78054 Villingen-Schwenningen, Germany.
  • Bonaterra GA; Institute of Anatomy and Cell Biology, Department of Medical Cell Biology, University of Marburg, Robert-Koch-Straße 8, D-35032 Marburg, Germany.
  • Kinscherf R; Institute of Anatomy and Cell Biology, Department of Medical Cell Biology, University of Marburg, Robert-Koch-Straße 8, D-35032 Marburg, Germany.
  • Laufer S; Pharmaceutical Institute, Department of Pharmaceutical Chemistry, University of Tuebingen, Auf der Morgenstelle 8, D-72076 Tuebingen, Germany.
  • Deigner HP; Furtwangen University, Medical and Life Sciences Faculty, Institute of Precision Medicine, Jakob-Kienzle-Str. 17, D-78054 Villingen-Schwenningen, Germany; Fraunhofer Institute IZI, Leipzig, EXIM Department, Schillingallee 68, D-18057 Rostock, Germany. Electronic address: hans-peter.deigner@hs-furtwa
Eur J Med Chem ; 153: 73-104, 2018 Jun 10.
Article en En | MEDLINE | ID: mdl-29031494
Ceramide generation is involved in signal transduction of cellular stress response, in particular during stress-induced apoptosis in response to stimuli such as minimally modified Low-density lipoproteins, TNFalpha and exogenous C6-ceramide. In this paper we describe 48 diverse synthetic products and evaluate their lysosomotropic and acid sphingomyelinase inhibiting activities in macrophages. A stimuli-induced increase of C16-ceramide in macrophages can be almost completely suppressed by representative compound NB 06 providing an effective protection of macrophages against apoptosis. Compounds like NB 06 thus offer highly interesting fields of application besides prevention of apoptosis of macrophages in atherosclerotic plaques in vessel walls. Most importantly, they can be used for blocking pH-dependent lysosomal processes and enzymes in general as well as for analyzing lysosomal dependent cellular signaling. Modulation of gene expression of several prominent inflammatory messengers IL1B, IL6, IL23A, CCL4 and CCL20 further indicate potentially beneficial effects in the field of (systemic) infections involving bacterial endotoxins like LPS or infections with influenza A virus.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esfingomielina Fosfodiesterasa / Apoptosis / Inhibidores Enzimáticos / Lisosomas Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2018 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esfingomielina Fosfodiesterasa / Apoptosis / Inhibidores Enzimáticos / Lisosomas Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2018 Tipo del documento: Article País de afiliación: Alemania