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Calpains Released by T Lymphocytes Cleave TLR2 To Control IL-17 Expression.
Perez, Joëlle; Dansou, Boris; Hervé, Roxane; Levi, Charlène; Tamouza, Houda; Vandermeersch, Sophie; Demey-Thomas, Emmanuelle; Haymann, Jean-Philippe; Zafrani, Lara; Klatzmann, David; Boissier, Marie-Christophe; Letavernier, Emmanuel; Baud, Laurent.
Affiliation
  • Perez J; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France;
  • Dansou B; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France;
  • Hervé R; UMR_S 1125, Université Paris 13, Sorbonne Paris Cité, F-93000 Bobigny, France; UMR_S 1125, INSERM, F-93000 Bobigny, France;
  • Levi C; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France;
  • Tamouza H; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France; Hôpital Tenon, Assistance Publique-Hôpitaux de Paris, F-75020 Paris, France;
  • Vandermeersch S; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France;
  • Demey-Thomas E; École supérieure de physique et de chimie industrielles de la ville de Paris/Spectrométrie de masse biologique et protéomique, F 75014 Paris, France;
  • Haymann JP; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France; Hôpital Tenon, Assistance Publique-Hôpitaux de Paris, F-75020 Paris, France;
  • Zafrani L; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France;
  • Klatzmann D; UMR_S 959 and Immunologie-Immunopathologie-Immunothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75005 Paris, France; Biotherapy and Département Inflammation-Immunopathologie-Biothérapie, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, F-75651 Paris, Fr
  • Boissier MC; UMR_S 1125, Université Paris 13, Sorbonne Paris Cité, F-93000 Bobigny, France; UMR_S 1125, INSERM, F-93000 Bobigny, France; Groupe Hospitalier Avicenne-Jean Verdier-René Muret, Assistance Publique-Hôpitaux de Paris, F-93000 Bobigny, France.
  • Letavernier E; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France; Hôpital Tenon, Assistance Publique-Hôpitaux de Paris, F-75020 Paris, France;
  • Baud L; UMR_S 1155 and Département Inflammation-Immunopathologie-Biothérapie, Université Pierre et Marie Curie Paris 06, Sorbonne Universités, F-75020 Paris, France; UMR_S 1155, INSERM, F-75020 Paris, France; Hôpital Tenon, Assistance Publique-Hôpitaux de Paris, F-75020 Paris, France; laurent.baud@tnn.aphp.
J Immunol ; 196(1): 168-81, 2016 Jan 01.
Article in En | MEDLINE | ID: mdl-26608921
ABSTRACT
Calpains are intracellular proteases that play a key role in inflammation/immunity. Rare studies show that they are partially externalized. However, the mechanism of this secretion and the functions of exteriorized calpains remain poorly understood. In this study, we found that mouse and human lymphocytes secreted calpains through an ABCA1-driven process. In turn, extracellular calpains inhibited IL-17A expression. We were able to attribute this function to a cleavage of the TLR2 extracellular domain, which prevented TLR2-induced transcription of molecules essential for IL-17A induction. Calpain exteriorization and TLR2 cleavage were critical for the control of IL-17A expression by low doses of IL-2. By using newly developed transgenic mice in which extracellular calpains are specifically inactivated, we provide evidence for the relevance of calpain externalization in vivo in regulating IL-17A expression and function in experimental sterile peritonitis and autoimmune arthritis, respectively. Thus, this study identifies calpain exteriorization as a potential target for immune modulation.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calpain / T-Lymphocytes / Interleukin-17 / Toll-Like Receptor 2 / ATP Binding Cassette Transporter 1 Type of study: Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: J Immunol Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calpain / T-Lymphocytes / Interleukin-17 / Toll-Like Receptor 2 / ATP Binding Cassette Transporter 1 Type of study: Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: J Immunol Year: 2016 Document type: Article