4.8 Article

Cyclophilins A, B, and C Role in Human T Lymphocytes Upon Inflammatory Conditions

Journal

FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.609196

Keywords

cyclophilin; inflammation; cyclophilin A inhibitors; CD147 receptor; T lymphocyte; migration

Categories

Funding

  1. FEDER
  2. Conselleria de Cultura, Educacion e Ordenacion Universitaria, Xunta de Galicia, Spain [2017 GRC GI-1682 (ED431C 2017/01)]
  3. Ministerio de Economia, Industria y Competitividad, Spain [ISCIII/PI19/01248, ISCIII/PI19/00879]
  4. European Union [Interreg AlertoxNet EAPA-317-2016, Interreg Agritox EAPA-998-2018, H2020 778069EMERTOX]
  5. FIDIS, Spain

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The study found that increased levels of CypA and CypB in T lymphocytes led to upregulation of the CD147 receptor, causing cell migration towards circulating CypA and CypB as chemoattractants, thus exacerbating the inflammatory response.
Cyclophilins (Cyps) are a group of peptidyl-prolyl cis/trans isomerases that play crucial roles in regulatory mechanisms of cellular physiology and pathology in several inflammatory conditions. Their receptor, CD147, also participates in the development and progression of the inflammatory response. Nevertheless, the main function of Cyps and their receptor are yet to be deciphered. The release of CypA and the expression of the CD147 receptor in activated T lymphocytes were already described, however, no data are available about other Cyps in these cells. Therefore, in the present work intra and extracellular CypA, B and C levels were measured followed by induced inflammatory conditions. After activation of T lymphocytes by incubation with concanavalin A, both intra and extracellular Cyps levels and the CD147 membrane receptor expression were increased leading to cell migration towards circulating CypA and CypB as chemoattractants. When CypA was modulated by natural and synthetic compounds, the inflammatory cascade was avoided including T cell migration. Our results strengthen the relationship between CypA, B, and C, their receptor, and the inflammatory process in human T lymphocytes, associating CypC with these cells for the first time.

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