Chemical Biology and Therapeutics Science Program, Broad Institute, Cambridge, MA.
Diabetes. 2024 Apr 1;73(4):585-591. doi: 10.2337/db23-0506.
Glucolipotoxicity (GLT), in which elevated levels of glucose and fatty acids have deleterious effects on β-cell biology, is thought to be one of the major contributors in progression of type 2 diabetes. In search of novel small molecules that protect β-cells against GLT, we previously discovered KD025, an inhibitor of Rho-associated coiled-coil-containing kinase isoform 2 (ROCK2), as a GLT-protective compound in INS-1E cells and dissociated human islets. To further understand the mechanism of action of KD025, we found that pharmacological and genetic inhibition of ROCK2 was not responsible for the protective effects of KD025 against GLT. Instead, kinase profiling revealed that KD025 potently inhibits catalytic subunits of casein kinase 2 (CK2), a constitutively active serine/threonine kinase. We experimentally verified that the inhibition of one of the catalytic subunits of casein kinase 2, CK2A1, but not CK2A2, improved cell viability when challenged with GLT. We conclude that KD025 inhibits CK2 to protect β-cells from GLT.
糖脂毒性(GLT),即升高的葡萄糖和脂肪酸水平对β细胞生物学产生有害影响,被认为是 2 型糖尿病进展的主要因素之一。为了寻找保护β细胞免受 GLT 损害的新型小分子化合物,我们之前在 INS-1E 细胞和分离的人胰岛中发现了 KD025,一种 Rho 相关卷曲螺旋激酶 2 同工型(ROCK2)的抑制剂,是一种 GLT 保护化合物。为了进一步了解 KD025 的作用机制,我们发现 ROCK2 的药理学和遗传抑制并不是 KD025 对抗 GLT 保护作用的原因。相反,激酶分析显示 KD025 能够强烈抑制酪蛋白激酶 2(CK2)的催化亚基,CK2 是一种组成性激活的丝氨酸/苏氨酸激酶。我们通过实验验证了当受到 GLT 挑战时,抑制其中一个酪蛋白激酶 2 的催化亚基,即 CK2A1,而非 CK2A2,可提高细胞活力。我们的结论是,KD025 通过抑制 CK2 来保护β细胞免受 GLT 损害。