Tlr2 deficiency is associated with enhanced elements of neuronal repair and caspase 3 activation following brain ischemia

Gorup, Dunja and Škokić, Siniša and Križ, Jasna and Gajović, Srećko (2019) Tlr2 deficiency is associated with enhanced elements of neuronal repair and caspase 3 activation following brain ischemia. Scientific Reports, 9 (1). p. 2821. ISSN 2045-2322

[img] PDF - Published Version
Download (2MB)

Abstract

The aim of this study was to apply multimodal in vivo imaging to assess the influence of altered innate immunity on brain repair after ischemic lesion. Tlr2-deficient mice were compared to wild type controls, as they lack Tlr2-mediated pro-inflammatory signaling triggered by postischemic necrosis. The ischemic lesion was induced by transient middle cerebral artery occlusion for 60 min, followed by brain imaging and analysis at four time points until 28 days after ischemia. Multimodal in vivo imaging involved a combination of 3 modalities: (1) magnetic resonance imaging by T2-weighted scans to assess brain lesion size, (2) bioluminescence imaging of Gap43-luc/gfp transgenic mice to visualize the axonal remodeling, and (3) caged-luciferin bioluminescence imaging of DEVD-luciferin allowing for visualization of caspase 3 and 7 activity in Gap43-luc/gfp mice. This enabled innovative correlation of the MRI-determined lesion size to photon fluxes obtained by bioluminescence imaging. Our data revealed that following ischemia, Tlr2-deficient mice had higher Gap43 expression and higher levels of caspases 3 and 7 activity, which was accompanied by enhanced levels of synaptic plasticity markers DLG4 and synaptophysin when compared to wild type controls. Altered inflammation in Tlr2-deficient mice was accompanied by enhanced elements of post-stroke repair, in particular during the chronic phase of recovery, but also with delayed final consolidation of the brain lesion.

Item Type: Article
Additional Information: © The Author(s) 2019. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Departments: Hrvatski institut za istraživanje mozga
Katedra za histologiju i embriologiju
Depositing User: Kristina Berketa
Status: Published
Creators:
CreatorsEmail
Gorup, DunjaUNSPECIFIED
Škokić, SinišaUNSPECIFIED
Križ, JasnaUNSPECIFIED
Gajović, SrećkoUNSPECIFIED
Date: 26 February 2019
Date Deposited: 25 Nov 2019 09:48
Last Modified: 25 Nov 2019 09:48
Subjects: /
Related URLs:
URI: http://medlib.mef.hr/id/eprint/3509

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year