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Koenigshofer, P.

Publications and source records attributed to Koenigshofer, P..

2 recordsLinked to original sources

Longitudinal investigation of spatial memory and retinal parameters in a 5xFAD model of Alzheimers disease reveals differences dependent on genotype and sex

SignificanceThe retinal phenotype of Alzheimers disease (AD) is poorly understood. The connection between spatial memory and retinal phenotype is poorly investigated. Additionally, the influence of sex on the disease in mouse models is not sufficiently clear and requires further investigation. AimTo investigate the retina and spatial memory of 5xFAD mouse models of AD by measuring retinal and behavioral parameters. ApproachA custom-built optical coherence tomography (OCT) system is used to image the retina of both eyes of 32 transgenic 5xFAD mice and 32 non-transgenic littermates over the course of 6 months (3-9 months of age) to investigate retinal parameters. The Morris Water Maze (MWM) test was performed to examine correlations between the retinal and spatial memory phenotype of the mouse model. ResultsData were acquired in the form of OCT reflectivity images and OCT angiograms as well as video recordings of the MWM test. Layer thickness and vascular density were calculated from the resulting data. Behavioral data was extracted from the videos acquired from the MWM. Total retinal and inner retinal layer thickness increased slightly over the measurement period, while outer retinal layer and retinal nerve fiber layer thickness showed no significant change. The correlation analysis between MWM and layer thickness data revelated a positive correlation between inner nuclear layer thickness and MWM test day parameters. ConclusionsOCT and MWM data revealed sex-based differences in the retinal phenotype of the 5xFAD mouse model, with changes in retinal thickness in different stages of the study and dissimilar correlations between retinal and spatial memory phenotype.

neuroscience↗

Transcriptomic signatures of progressive and regressive liver fibrosis and portal hypertension

Persistent liver injury triggers a fibrogenic program that causes pathologic remodelling of the hepatic microenvironment (i.e., liver fibrosis) and portal hypertension. The dynamics of gene regulation during liver disease progression and regression remain understudied. Here, we generated hepatic transcriptome profiles in two well-established liver disease models at peak fibrosis and during spontaneous regression after the removal of the inducing agents. We linked the dynamics of key liver disease readouts, such as portal pressure, collagen proportionate area, and transaminase serum levels, to most differentially expressed genes, enabling the identification of transcriptomic signatures of progressive vs. regressive liver fibrosis and portal hypertension. These candidate biomarkers (e.g., Scube1, Tcf4, Src, Hmga1, Trem2, Mafk, Mmp7) were also validated in RNA-seq datasets of patients with cirrhosis and portal hypertension. Finally, deconvolution analysis identified major cell types and suggested an association of macrophage and portal hepatocyte signatures with portal hypertension and fibrosis area in both models.

systems biology↗