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Protean proteases: at the cutting edge of lung diseases.
Taggart, Clifford; Mall, Marcus A; Lalmanach, Gilles; Cataldo, Didier; Ludwig, Andreas; Janciauskiene, Sabina; Heath, Nicole; Meiners, Silke; Overall, Christopher M; Schultz, Carsten; Turk, Boris; Borensztajn, Keren S.
Afiliação
  • Taggart C; Airway Innate Immunity Research group (AiiR), Centre for Experimental Medicine, Queen's University Belfast, UK.
  • Mall MA; Dept of Translational Pulmonology, University of Heidelberg, Heidelberg, Germany.
  • Lalmanach G; Division of Pediatric Pulmonology & Allergy and Cystic Fibrosis Center, Dept of Pediatrics, University of Heidelberg, Heidelberg, Germany.
  • Cataldo D; Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
  • Ludwig A; INSERM UMR1100 Centre d'Etude des Pathologies Respiratoires (CEPR), Equipe: Mécanismes Protéolytiques dans l'Inflammation, Université François Rabelais, Tours, France.
  • Janciauskiene S; Laboratory of Tumors and Development and Dept of Respiratory Diseases, University of Liege, Liege, Belgium.
  • Heath N; Inflammation Pharmacology Research Group, Institute of Pharmacology and Toxicology, RWTH Aachen University, Aachen, Germany.
  • Meiners S; Dept of Respiratory Medicine, a member of The German Center for Lung Research (DZL), Hannover Medical School, Hannover, Germany.
  • Overall CM; Division of Pediatric Pulmonology & Allergy and Cystic Fibrosis Center, Dept of Pediatrics, University of Heidelberg, Heidelberg, Germany.
  • Schultz C; Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
  • Turk B; European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
  • Borensztajn KS; Comprehensive Pneumology Center (CPC), University Hospital, Ludwig-Maximilians University, Helmholtz Zentrum München, Member of the German Center for Lung Research (DZL), Munich, Germany.
Eur Respir J ; 49(2)2017 02.
Article em En | MEDLINE | ID: mdl-28179435
Proteases were traditionally viewed as mere protein-degrading enzymes with a very restricted spectrum of substrates. A major expansion in protease research has uncovered a variety of novel substrates, and it is now evident that proteases are critical pleiotropic actors orchestrating pathophysiological processes. Recent findings evidenced that the net proteolytic activity also relies upon interconnections between different protease and protease inhibitor families in the protease web.In this review, we provide an overview of these novel concepts with a particular focus on pulmonary pathophysiology. We describe the emerging roles of several protease families including cysteine and serine proteases.The complexity of the protease web is exemplified in the light of multidimensional regulation of serine protease activity by matrix metalloproteases through cognate serine protease inhibitor processing. Finally, we will highlight how deregulated protease activity during pulmonary pathogenesis may be exploited for diagnosis/prognosis purposes, and utilised as a therapeutic tool using nanotechnologies.Considering proteases as part of an integrative biology perspective may pave the way for the development of new therapeutic targets to treat pulmonary diseases related to intrinsic protease deregulation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metaloproteinases da Matriz / Pulmão / Pneumopatias Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Eur Respir J Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metaloproteinases da Matriz / Pulmão / Pneumopatias Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Eur Respir J Ano de publicação: 2017 Tipo de documento: Article