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Kriska, J.

Publications and source records attributed to Kriska, J..

4 recordsLinked to original sources

Canonical Wnt signaling controls the fate and plasticity of NG2 glia in the healthy and ischemic adult mouse cortex

NG2 glia, also known as oligodendrocyte precursor cells (OPCs), exhibit unexpected plasticity in the adult brain after injury, yet the molecular cues guiding their fate remain poorly defined. Wnt signaling contributes to tissue responses following ischemic stroke, but its precise role in post-injury glial remodeling is not fully understood. Here, we define how Wnt/{beta}-catenin signaling shapes NG2 glial behavior after focal cerebral ischemia. Using genetic mouse models enabling cell-specific Wnt pathway activation or inhibition, combined with single-cell RNA sequencing, immunohistochemistry, and electrophysiological recording, we disclosed a central role for Wnt signaling in post-injury fate specification. We identified 12 transcriptionally distinct subpopulations within the oligodendroglial lineage, including a subset with an astrocyte-like transcriptional profile. Wnt signaling strongly influenced the balance between OPC proliferation and differentiation: pathway hyperactivation impaired oligodendrocyte maturation and expanded astrocyte-like NG2-derived cells, likely through concomitant activation of the Notch pathway. Remarkably, Wnt hyperactivation also induced the appearance of cholinergic neuron-like cells derived from NG2-expressing cells exclusively in the somatosensory cortex; these cells generated action potentials and exhibited sodium conductance characteristic of functional neurons. Together, these findings demonstrate that NG2 glia undergo distinct fate transitions after stroke and that their lineage plasticity is highly sensitive to Wnt pathway dynamics. Targeted fine-tuning of Wnt/{beta}-catenin signaling may enable directed redirection of NG2 glia toward specific reparative outcomes, including neuronal reprogramming, in the injured adult brain. TEASERWnt activation promotes neuronal conversion of NG2 glia, while impairing oligodendrocyte maturation.

neuroscience↗

PU.1-driven enrichment enables microglia profiling from frozen brain tissue using the high-throughput Smart-seq3xpress method

Single-cell transcriptomics has revealed the central role of microglia in brain development, homeostasis, and disease, particularly in the context of neuroinflammation. While single-cell RNA-sequencing enables targeted microglial analysis from fresh tissue, studying these cells in cryopreserved or archival samples remains challenging due to the lack of protocols for their specific enrichment. We introduce a method for the selective isolation of microglial nuclei from fresh-frozen brain tissue using the transcription factor PU.1 as a nuclear marker. To stabilize PU.1 for reliable detection, a brief formaldehyde fixation step is applied. The protocol is fully compatible with Smart-seq3xpress, a high-sensitivity, full-length transcriptomic method offering isoform- and allele-level resolution, making the workflow scalable and cost-efficient. We benchmarked the method in a mouse model of ischemic stroke, evaluating both technical performance and its ability to capture biologically meaningful microglial states. Compared to standard single-nucleus protocols, our approach yielded higher gene and UMI counts and a greater proportion of coding reads. Transcriptomic profiles closely matched those from whole-cell RNA-sequencing including the detection of activation markers and diverse microglial subpopulations. This approach addresses key limitations of single-nucleus RNA - sequencing and opens new possibilities for studying microglial states in cryopreserved and archival brain tissue, broadening access to cellular insights in both basic and translational research.

neuroscience↗

Astrocyte-like subpopulation of NG2 glia in the adult mouse cortex exhibits characteristics of neural progenitor cells and is capable of forming neuron-like cells after ischemic injury

Glia cells expressing neuron-glial antigen 2 (NG2) play a critical role as oligodendrocyte precursor cells (OPCs) in the healthy brain; however, their differentiation potential after ischemic injury remains an unresolved question. Here, we aimed to elucidate the heterogeneity and role of NG2 glia in the ischemic brain. We used transgenic mice to label NG2-expressing cells and their progeny with red fluorescent protein tdTomato in the healthy brains and those after focal cerebral ischemia (FCI). Based on single-cell RNA sequencing, the labeled glial cells were divided into five distinct subpopulations. The identity of these subpopulations was determined based on gene expression patterns. In addition, membrane properties were further analyzed using the patch-clamp technique. Three of the observed subpopulations represented OPCs, whereas the fourth group exhibited characteristics of cells destined for oligodendrocyte fate. The fifth subpopulation of NG2 glia carried astrocytic markers. Importantly, we detected features of neural progenitors in these cells. This subpopulation was present in both healthy and post-ischemic tissue; however, its gene expression changed after ischemia, with genes related to neurogenesis being more abundant. Neurogenic gene expression was monitored over time and complemented by immunohistochemical staining, which showed increased numbers of Purkinje cell protein 4-positive NG2 cells at the edge of the ischemic lesion 12 days after FCI, and NeuN-positive NG2 cells 28 days after injury, indicating the existence of neuron-like cells that develop from NG2 glia in the ischemic tissue. Our results provide further insight into the differentiation plasticity and neurogenic potential of NG2 glia after stroke. Main PointsO_LIDifferent subpopulations of NG2 glia in the healthy and ischemic adult cortex were identified based on their gene expression and membrane properties. C_LIO_LIAstrocyte-like NG2 glia exhibit neurogenic gene expression and are more abundant in post-ischemic tissue. C_LIO_LIProgeny of NG2-positive cells carrying neuronal marker NeuN was observed at the edge of the ischemic lesion. C_LI

neuroscience↗

Decoding the transcriptional response to ischemic stroke in young and aged mouse brain

Ischemic stroke is one of the leading causes of mortality and major healthcare and economic burden. It is a well-recognized disease of aging, yet it is unclear how the age-dependent vulnerability occurs and what are the underlying mechanisms. To address these issues, we performed a comprehensive RNA-Seq analysis of aging, ischemic stroke and their interaction using a model of permanent middle cerebral artery occlusion (MCAO) in 3 and 18 month old female mice. We assessed differential gene expression across injury status and age, estimated cell type proportion changes, assayed the results against a range of transcriptional signatures from the literature and performed unsupervised co-expression analysis, identifying modules of genes with varying response to injury. We uncovered selective vulnerability of neuronal populations and increased activation of type-I interferon (IFN-I) signaling and several other inflammatory pathways in aged mice. We extended these findings via targeted expression analysis in tissue as well as acutely purified cellular populations to show differential temporal dynamics of IFN-I signaling between age groups and contribution of individual cell types. Together, these results paint a picture of ischemic stroke as a complex age-related disease and provide insights into interaction of aging and stroke on cellular and molecular level.\n\nGraphical summary\n\nO_FIG O_LINKSMALLFIG WIDTH=156 HEIGHT=200 SRC=\"FIGDIR/small/769331v1_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (46K):\norg.highwire.dtl.DTLVardef@1590c10org.highwire.dtl.DTLVardef@126fc76org.highwire.dtl.DTLVardef@88e20aorg.highwire.dtl.DTLVardef@b000d9_HPS_FORMAT_FIGEXP M_FIG C_FIG

genomics↗