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Biology subjects

Moraes, B. C.

Publications and source records attributed to Moraes, B. C..

2 recordsLinked to original sources

Automated compartment-based quantification reveals distinct patterns of cutaneous innervation with aging and microbial colonization

Cutaneous innervation is commonly quantified using measures such as intraepidermal nerve fiber density, but these approaches capture only selected anatomical regions or features of nerve structure. We developed an automated image-analysis pipeline to quantify nerve area and nerve-skeleton length across defined epidermal and dermal compartments in whole, stitched mouse plantar skin sections. Automated epidermis-dermis boundary detection showed agreement with manual tracing within the range of inter-observer variation and produced similar downstream measurements. We then applied the pipeline to skin from mice across age and distinct microbial environmental exposures. Conventionalized mice exposed to microbes had greater nerve area and length than germ-free mice in both the epidermis and dermis. In the aging cohort, aged mice had greater dermal nerve area and length than young mice, while epidermal measurements did not differ significantly. We also analyzed the epidermis and dermis together to assess whole-skin innervation. Whole-skin nerve area and length were higher in conventionalized mice than in germ-free mice but did not differ significantly between young and aged mice. These findings show that analyzing the epidermis and dermis separately helps identify where nerve measurements differ, including differences that may not be detected when both skin layers are analyzed together. Compartment-resolved quantification therefore provides a complementary approach for studying changes in cutaneous innervation across biological conditions and behavioral outcomes.

neuroscience↗

Sexually dimorphic regulatory T cell-derived enkephalin imparts pregnancy-induced analgesia

T cells have emerged as sex-dependent orchestrators of pain chronification but the sexually dimorphic mechanisms by which T cells control pain sensitivity is not resolved. Here, we demonstrate an influence of regulatory T cells (Tregs) on pain processing that is distinct from their canonical functions of immune regulation and tissue repair. Specifically, meningeal Tregs (mTregs) express the endogenous opioid, enkephalin, and mTreg-derived enkephalin exerts an antinociceptive action through a presynaptic opioid receptor signaling mechanism that is dispensable for immunosuppression. We demonstrate that mTregs are both necessary and sufficient to suppress mechanical pain sensitivity in female, but not male, mice, with this modulation reliant on sex hormones. These results uncover a fundamental sex-specific, and immunologically- derived endogenous opioid circuit for nociceptive regulation with critical implications for pain biology. Highlights1. Gating of allodynia by meningeal Tregs is sex hormone-dependent 3. Treg-derived enkephalin modulates mechanical pain sensitivity, not inflammation 4. Delta opioid receptor on MrgprD+ sensory neuron mediates pain processing by mTregs

immunology↗