| 研究実績の概要 |
The purpose of this research is to further understand regulatory T cell (Tregs) function in the skin during steady state and inflammatory conditions. Briefly, Treg behavior was visualized via a two-photon microscope in the ear skin of a live mouse using various Treg-specific fluorescent reporter mice during the contact hypersensitivity skin inflammatory response. Treg colocalization and interactions with dermal dendritic cells (DCs) was investigated via immunohistochemistry, and the combination of Treg and DC reporter mice.
The Treg-Cre recombinase mouse (Foxp3-Cre) was also crossed with a R26-LSL-Gi-DREADD mouse to enable chemical inactivation of chemokine signaling to inhibit Treg migration in the skin. However issues with stochastic activity in the Foxp3-Cre mouse rendered the newly generated mouse unreliable as Gi-DREADD insertion was no longer Treg specific.
While studying the relationship between sensory nerves and the immune system, we made a novel observation that chemical denervation with resiniferatoxin (RTX) induced hair loss in mice. Subsequent regrown hair in these bald areas were permenantly pigmented, suggesting a dysfunction in melanocyte stem cells of the affected hair follicles. As Tregs are known to reside around the hair follicle and support hair follicle cycling, we depleted Tregs prior to and during RTX-administration. Surprisingly, Treg-depleted mice had delayed hair regrowth, but regrown hair was still depigmented. This suggests that while Tregs may be important for hair follicle stem cells, they do not affect melanocyte stem cells in the follicle.
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