Nature Neuroscience

Nature Neuroscience, Published online: 08 September 2026; doi:10.1038/s41593-026-02418-6 Although Alzheimer’s disease (AD) is a disease of the brain, we demonstrate that it disrupts myeloid cell production in the bone marrow via a type I interferon signal, preventing protective monocyte-derived macrophages from reaching the brain. Blocking this signal in the 5xFAD mouse model of amyloidosis resto…

Nature Neuroscience, Published online: 08 September 2026; doi:10.1038/s41593-026-02428-4 Intestinal CD4+ T cells migrate to the dura and brain following gut infection with bacteria or parasites, establishing a long-lived memory population capable of proliferation and cytokine production following rechallenge with bloodborne pathogens.

Nature Neuroscience, Published online: 08 September 2026; doi:10.1038/s41593-026-02417-7 Alzheimer’s disease progression involves reduced bone marrow production of myeloid cells due to type I interferon signaling, which hampers the homing of protective immune cells to the affected brain. In a mouse model, inhibiting this pathway restored immune cell recruitment and halted disease progression.

Nature Neuroscience, Published online: 07 September 2026; doi:10.1038/s41593-026-02447-1 Implanted brain–computer interfaces hold great promise for restoring communication and other functions and for revealing new aspects of human brain physiology. Yet as the number of implantations in humans expands, ethical clarity must keep pace with technical ambition. We propose that this should involve dist…

Aaron P. Batista
4d ago

Nature Neuroscience, Published online: 04 September 2026; doi:10.1038/s41593-026-02442-6 Why some skills are easier to learn than others remains a central question in neuroscience. Busch and colleagues demonstrate that the intrinsic geometry of human brain activity shapes learning, thereby facilitating adaptation that remains within existing neural manifolds while limiting learning beyond them.

Nature Neuroscience, Published online: 01 September 2026; doi:10.1038/s41593-026-02419-5 The authors used whole-exome sequencing and analysis of rare coding variation in individuals with obsessive–compulsive disorder and chronic tic disorders, including Tourette disorder, to identify 36 large-effect risk genes, highlighting both shared genetic risks and convergent biology.

Nature Neuroscience, Published online: 25 August 2026; doi:10.1038/s41593-026-02413-x Social isolation recruits a basolateral amygdala–medial prefrontal cortex circuit to escalate alcohol drinking in male mice. This pathway reshapes prefrontal population dynamics, suppressing natural reward responses while amplifying alcohol-evoked activity.

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