Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/124240
Title: Inflammatory Gene Expression In Whole Peripheral Blood At Early Stage Of Sporadic Amyotrophic Lateral Sclerosis
Author: Andrés Benito, Pol
Moreno Castro, Jesús
Domínguez, Raúl
Asó, Ester
Povedano, Mònica
Ferrer, Isidro (Ferrer Abizanda)
Keywords: Esclerosi lateral amiotròfica
Citoquines
Amyotrophic lateral sclerosis
Cytokines
Issue Date: 13-Oct-2017
Publisher: Frontiers Media
Abstract: Objective: Characterization of altered expression of selected transcripts linked to inflammation in the peripheral blood of sporadic amyotrophic lateral sclerosis (sALS) patients at early stage of disease to increase knowledge about peripheral inflammatory response in sALS. Methods: RNA expression levels of 45 genes were assessed by RT-qPCR in 22 sALS cases in parallel with 13 age-matched controls. Clinical and serum parameters were assessed at the same time. Results: Upregulation of genes coding for factors involved in leukocyte extravasation (ITGB2, INPP5D, SELL, and ICAM1) and extracellular matrix remodeling (MMP9 and TIMP2), as well as downregulation of certain chemokines (CCL5 and CXC5R), antiinflammatory cytokines (IL10, TGFB2, and IL10RA), pro-inflammatory cytokines (IL-6), and T-cell regulators (CD2 and TRBC1) was found in sALS cases independently of gender, clinical symptoms at onset (spinal, respiratory, or bulbar), progression, peripheral leukocyte number, and integrity of RNA. MMP9 levels positively correlated with age, whereas CCR5, CCL5, and TRBC1 negatively correlated with age in sALS but not in controls. Relatively higher TNFA expression levels correlate with higher creatinine kinase protein levels in plasma. Conclusion: Present findings show early inflammatory responses characterized by upregulation of factors enabling extravasation of leukocytes and extracellular matrix remodeling in blood in sALS cases, in addition to increased TNFA levels paralleling skeletal muscle damage.
Note: Reproducció del document publicat a: https://doi.org/10.3389/fneur.2017.00546
It is part of: Frontiers in Neurology, 2017, vol. 8
URI: http://hdl.handle.net/2445/124240
Related resource: https://doi.org/10.3389/fneur.2017.00546
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Patologia i Terapèutica Experimental)

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