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Bloss, E.

Publications and source records attributed to Bloss, E..

2 recordsLinked to original sources

Conserved synaptic modifications by humanized tau through diverse isoform- and mutation-specific intracellular interactions

Mutations in the microtubule-binding protein tau are considered causal for a diverse group of neurodegenerative diseases collectively referred to as primary tauopathies. Specific tauopathies are associated with different mutations, distinct tau isoforms, manifest in unique cellular and circuit-wide patterns of degeneration, and present with specific clinical symptoms and trajectories. The mechanisms that link variations in the primary tau protein structure to distinct forms of neural circuit dysfunction remain largely unknown. Here, we created an orthogonal viral resource to systematically examine the impact of expressing humanized tau isoforms harboring different disease-relevant mutations in excitatory pyramidal cells from the mouse prelimbic cortex. We used these reagents to show that expression of mutant humanized tau (hTau) as either of two isoforms produced very similar patterns of circuit-specific synaptic disconnection on cortical projection neurons. However, mass spectrometry revealed that the interactomes of these different tau species varied markedly as functions of isoform, mutation, and subcellular location. We validated the functional relevance of increased hTau interactions with mitochondrial proteins in induced neurons differentiated from Ngn2-iPSCs expressing different hTau constructs. These results suggest different disease-relevant hTau proteins likely use distinct mechanisms to drive a highly stereotyped form of synapse loss in cortical neurons.

neuroscience↗

Activity-dependent subcellular compartmentalization of dendritic mitochondria structure in CA1 pyramidal neurons

Neuronal mitochondria play important roles beyond ATP generation, including Ca2+ uptake, and therefore have instructive roles in synaptic function and neuronal response properties. Mitochondrial morphology differs significantly in the axon and dendrites of a given neuronal subtype, but in CA1 pyramidal neurons (PNs) of the hippocampus, mitochondria within the dendritic arbor also display a remarkable degree of subcellular, layer- specific compartmentalization. In the dendrites of these neurons, mitochondria morphology ranges from highly fused and elongated in the apical tuft, to more fragmented in the apical oblique and basal dendritic compartments, and thus occupy a smaller fraction of dendritic volume than in the apical tuft. However, the molecular mechanisms underlying this striking degree of subcellular compartmentalization of mitochondria morphology are unknown, precluding the assessment of its impact on neuronal function. Here, we demonstrate that this compartment-specific morphology of dendritic mitochondria requires activity-dependent, Camkk2- dependent activation of AMPK and its ability to phosphorylate two direct effectors: the pro-fission Drp1 receptor Mff and the recently identified anti-fusion, Opa1-inhibiting protein, Mtfr1l. Our study uncovers a new activity- dependent molecular mechanism underlying the extreme subcellular compartmentalization of mitochondrial morphology in dendrites of neurons in vivo through spatially precise regulation of mitochondria fission/fusion balance.

cell biology↗