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Karhula, J.

Publications and source records attributed to Karhula, J..

2 recordsLinked to original sources

Machine learning on magnetoencephalography data yields generalizable low-dimensional neural fingerprints that distinguish individuals across task conditions

Individual brains are unique in structure and function. Functional differences are captured by neural fingerprints, which reflect individual differences in behavior and cognition as well as group-level changes related to neurodegenerative diseases. Most research efforts so far have focused on fingerprints com-prising full functional connectomes. However, the high dimensionality of the connectomes can increase computational load and impede performance of machine learning methods in potential applications. A low-dimensional alternative that retains individual features of the full connectomes would thus be beneficial. The present study employed latent-noise Bayesian Reduced Rank Regression (lnBRRR) to learn low-dimensional latent spaces that capture individual features in functional connectivity and power spectral density data derived from MEG recordings. LnBRRR performance was assessed with low training set sizes (N=20-44), and against principal component analysis and linear discriminant analysis. Model performance was also assessed with task data, and the solutions were compared across task conditions with cosine similarity to establish whether individual features are altered by different cognitive processes. LnBRRR captured generalizable individual patterns already at N=20 but N=30-35 was needed to reach optimal test accuracies and to prevent potential overfitting. The model also achieved comparable performance to the alternative models. Latent fingerprints derived from task data attained comparable performance to resting-state latent fingerprints, and lnBRRR solutions were shown to generalize across conditions. Additionally, the model solutions for power spectral density data were discovered to be notably similar, yet differently rotated, over task conditions, suggesting that similar patterns of individual features were captured by the model regardless of the task condition. Altogether, the present results highlight lnBRRR as a potential tool for neuroimaging data analysis and demonstrate that individual differences in power spectral density are largely intrinsic and unaffected by varying cognitive processes.

neuroscience↗

Embryonic macrophages in brown adipose tissue are spatially associated with developing nerves

Brown adipose tissue (BAT) is a specialized adipose tissue that produces heat through sympathetic nerve-dependent thermogenesis and influences glucose and triglyceride metabolism, making it a potential target for obesity-related diseases. In mice, interscapular BAT (iBAT) emerges on embryonic days (E)14.5-15.5, with extensive vessel and nerve networks still maturing postnatally. These developmental stages are critical for BAT, impacting long-term BAT function. In adult mice, macrophages regulate sympathetic innervation and thermogenesis. However, research on BAT macrophage characters, ontogeny, and functions in early life is lacking. Using single-cell genomics and proteomics, fate-mapping techniques, and 3D imaging, we analyzed iBAT macrophages during early development. We discovered the presence of fetal liver-derived macrophages as early as E15.5, which are later fully replaced by bone marrow-derived macrophages. Transcriptomics data highlight mononuclear phagocyte subpopulations, from which most express macrophage-associated genes (Adgre1, Fcgr1, Csf1r) and monocytic markers (Ccr2, Ly6c2) together. Embryonic macrophages interact closely with developing neural networks, while postnatal bone marrow-derived macrophages associate with blood vessels. Lack of fetal liver-derived macrophages disrupts nerve and vessel development and causes downregulation of genes related to neuronal diseases and protein digestion pathways. Our data suggest that fetal liver-derived macrophages, interacting with BATs developing sympathetic neural network, guide the development of tissue morphology. Understanding further the mechanism behind these events can unravel novel targets for BAT immunomodulation.

immunology↗