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Biology subjects

Nakajo, H.

Publications and source records attributed to Nakajo, H..

3 recordsLinked to original sources

An orthogonal Cro/OR3 binary system for targeted gene expression

Precise spatiotemporal control of gene expression is essential for dissecting complex biological systems. Here, we introduce a phage-derived Cro/OR3 binary system for transcriptional activation that functions robustly in zebrafish and human cells. A Cro repressor fused to the VP16 activation domain efficiently drives expression of OR3 operator-linked genes, and its activity can be targeted to specific cell types using enhancer-trap and promoter-controlled zebrafish lines. As a proof of concept, we manipulate glutamate transporter Glast/Slc1a3b-expressing cells in the central nervous system by Cro/OR3-mediated expression of a human ataxia-associated, uptake-deficient Glast/Slc1a3b variant, causing spastic, uncoordinated movement and axial deformation. Concurrent Gal4/UAS-mediated visualization reveals substantially disrupted positioning of motor neurons, highlighting their selective sensitivity to extracellular glutamate homeostasis during spinal circuit assembly. Together, these results establish the Cro/OR3 system as an orthogonal platform for targeted gene expression, enabling precise mechanistic dissection of how specific cell types and their interactions underlie diverse biological processes.

bioengineering↗

Extracellular matrix proteolysis maintains synapse plasticity during brain development

Maintaining a dynamic neuronal synapse pool is critical to brain development. The extracellular matrix (ECM) regulates synaptic plasticity via mechanisms that are still being defined and are studied predominantly in adulthood. Using live imaging of excitatory synapses in zebrafish hindbrain we observed a bimodal distribution of short-lived (dynamic) and longer-lived (stable) synapses. Disruption of ECM via digestion or brevican deletion destabilized dynamic but not stable synapses and led to decreased synapse density. Conversely, loss of matrix metalloproteinase 14 (MMP14) led to accumulation of brevican and increased the stable synapse pool, resulting in increased synapse density. Microglial MMP14 was essential to these effects in both fish and human iPSC-derived cultures. Both MMP14 and brevican were required for experience-dependent synapse plasticity in a motor learning assay. These data, complemented by mathematical modeling, define an essential role of ECM remodeling in maintaining a dynamic subset of synapses during brain development.

neuroscience↗

Microglial cathepsin B promotes neuronal efferocytosis during brain development

Half of all newborn neurons in the developing brain are removed via efferocytosis - the phagocytic clearance of apoptotic cells. Microglia are brain-resident professional phagocytes that play important roles in neural circuit development including as primary effectors of efferocytosis. While the mechanisms through which microglia recognize potential phagocytic cargo are widely studied, the lysosomal mechanisms that are necessary for efficient digestion are less well defined. Here we show that the lysosomal protease cathepsin B promotes microglial efferocytosis of neurons and restricts the accumulation of apoptotic cells during brain development. We show that cathepsin B is microglia-specific and enriched in brain regions where neuronal turnover is high in both zebrafish and mouse. Myeloid-specific cathepsin B knockdown in zebrafish led to dysmorphic microglia containing undigested dead cells, as well as an accumulation of dead cells in surrounding tissue. These effects where phenocopied in mice globally deficient for Ctsb using markers for apoptosis. We also observed behavioral impairments in both models. Live imaging studies in zebrafish revealed deficits in phagolysosomal fusion and acidification, and live imaging of cultured mouse microglia reveal delayed phagocytosis consistent with impairments in digestion and resolution of phagocytosis rather than initial uptake. These data reveal a novel role for microglial cathepsin B in mediating neuronal efferocytosis during typical brain development.

neuroscience↗