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<i>Trpv1</i>-dependent <i>Cacna1b</i> gene inactivation reveals cell-specific functions of Ca<sub>V</sub>2.2 channels <i>in vivo</i>

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Taylor & Francis Group2025-12-22 更新2026-04-16 收录
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Voltage-gated Ca<sub>V</sub>2.2 channels underlie the N-type current, and they regulate calcium entry at many presynaptic nerve endings to control transmitter release. A role for Ca<sub>V</sub>2.2 channels has been well established in the transmission of sensory signals including noxious information using pharmacological and global gene knockout mouse models. However, investigation of the cell-specific actions of Ca<sub>V</sub>2.2 channels has been difficult due to the lack of gene-dependent knockout mouse models and particularly in dissecting behavioral responses that depend on Ca<sub>V</sub>2.2 channel activity. Here, we show the importance of Ca<sub>V</sub>2.2 channels in <i>Trpv1</i>-lineage neurons in behavioral responses to sensory stimuli using Cre-dependent inactivation of the <i>Cacna1b</i> gene. Our work shows the cell-type specificity of Ca<sub>V</sub>2.2 channels in mediating rapidly developing heat hypersensitivity and the utility of Cre-dependent inactivation of <i>Cacna1b</i> to discern cell-specific Ca<sub>V</sub>2.2 channel functions.

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2025-12-22
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