Department of Medicine, Division of Cardiology.
Consortium for Fibrosis Research & Translation, and.
J Clin Invest. 2023 Oct 2;133(19):e168192. doi: 10.1172/JCI168192.
Stimulation of adipocyte β-adrenergic receptors (β-ARs) induces expression of uncoupling protein 1 (UCP1), promoting nonshivering thermogenesis. Association of β-ARs with a lysine-myristoylated form of A kinase-anchoring protein 12 (AKAP12, also known as gravin-α) is required for downstream signaling that culminates in UCP1 induction. Conversely, demyristoylation of gravin-α by histone deacetylase 11 (HDAC11) suppresses this pathway. Whether inhibition of HDAC11 in adipocytes is sufficient to drive UCP1 expression independently of β-ARs is not known. Here, we demonstrate that adipocyte-specific deletion of HDAC11 in mice leads to robust induction of UCP1 in adipose tissue (AT), resulting in increased body temperature. These effects are mimicked by treating mice in vivo or human AT ex vivo with an HDAC11-selective inhibitor, FT895. FT895 triggers biphasic, gravin-α myristoylation-dependent induction of UCP1 protein expression, with a noncanonical acute response that is posttranscriptional and independent of protein kinase A (PKA), and a delayed response requiring PKA activity and new Ucp1 mRNA synthesis. Remarkably, HDAC11 inhibition promotes UCP1 expression even in models of adipocyte catecholamine resistance where β-AR signaling is blocked. These findings define cell-autonomous, multimodal roles for HDAC11 as a suppressor of thermogenesis, and highlight the potential of inhibiting HDAC11 to therapeutically alter AT phenotype independently of β-AR stimulation.
脂肪细胞 β-肾上腺素能受体(β-ARs)的刺激会诱导解偶联蛋白 1(UCP1)的表达,促进非颤抖性产热。β-ARs 与蛋白激酶 A 锚定蛋白 12 的赖氨酸肉豆蔻酰化形式(AKAP12,也称为gravin-α)的关联是下游信号转导所必需的,该信号转导最终导致 UCP1 的诱导。相反,组蛋白去乙酰化酶 11(HDAC11)对 gravin-α 的去肉豆蔻酰化会抑制该途径。脂肪细胞中 HDAC11 的抑制是否足以独立于 β-AR 驱动 UCP1 的表达尚不清楚。在这里,我们证明了小鼠脂肪细胞特异性敲除 HDAC11 会导致脂肪组织(AT)中 UCP1 的强烈诱导,从而导致体温升高。体内或人体 AT 体外用 HDAC11 选择性抑制剂 FT895 处理会模拟这些效果。FT895 触发 UCP1 蛋白表达的两相、gravin-α 肉豆蔻酰依赖性诱导,具有非典型的急性反应,是转录后且独立于蛋白激酶 A(PKA)的,以及需要 PKA 活性和新的 Ucp1 mRNA 合成的延迟反应。值得注意的是,HDAC11 抑制即使在β-AR 信号阻断的脂肪细胞儿茶酚胺抵抗模型中也能促进 UCP1 的表达。这些发现定义了 HDAC11 作为产热抑制剂的细胞自主、多模式作用,并强调了抑制 HDAC11 独立于 β-AR 刺激治疗性改变 AT 表型的潜力。