The Psychiatric Institute, University of Illinois at Chicago, Chicago, IL, USA.
Jesse Brown Veterans Affairs Medical Center, Chicago, IL, USA.
Clin Exp Immunol. 2019 Apr;196(1):67-75. doi: 10.1111/cei.13250. Epub 2019 Feb 3.
Epigenetic effects of anti-psychotic medications are poorly understood. We have appropriated a model whereby heterochromatin is established through 24- or 48-h lipopolysaccharide (LPS) treatment, and tested the epigenetic effects of risperidone along the adenylyl cyclase/protein kinase A (AC/PKA) pathway in human liposarcoma cells that express the LPS-sensitive Toll-like receptor (TLR)-4. Human SW872 cells were cultured with LPS and mRNA expression levels and epigenetic modifications of dimethylated lysine 9 of histone 2 (H3K9me2), geterochromatin protein 1γ (HP1γ) and phospho-H3S10 at promoters of interleukin (IL)-6, tumor necrosis factor (TNF)-α and IL1β were measured. Pharmacological manipulation of the AC/PKA pathway was achieved through treatment with a PKA inhibitor (H89), mitogen- and stress-activated kinase 1 (MSK1) inhibitor (SB-747651A) or forskolin. Twenty-four and 48-h LPS treatment establishes heterochromatin at selected promoters, corresponding to decreased mRNA expression. Concurrent risperidone treatment with LPS treatment can both 'block' and 'reverse' heterochromatin formation. Forskolin treatment resulted in a similar disassembling effect on heterochromatin. Conversely, inhibition of PKA by H89 or MSK1 both blocked 'normalizing' effects of risperidone on LPS-induced heterochromatin. Our results demonstrate that risperidone can disassemble heterochromatin, exerting this effect along the G-protein/AC/PKA pathway. This approach can also be utilized to investigate functional outcomes of single or combined pharmacological treatments on chromatin assemblies in human cells.
抗精神病药物的表观遗传效应知之甚少。我们采用了一种模型,即通过 24 或 48 小时脂多糖 (LPS) 处理建立异染色质,并在表达 LPS 敏感 Toll 样受体 (TLR)-4 的人脂肪肉瘤细胞中沿腺苷酸环化酶/蛋白激酶 A (AC/PKA) 途径测试利培酮的表观遗传效应。将人 SW872 细胞用 LPS 培养,测量 IL-6、TNF-α 和 IL1β 启动子上组蛋白 2 (H3) 赖氨酸 9 二甲基化 (H3K9me2)、异染色质蛋白 1γ (HP1γ) 和磷酸化 H3S10 的 mRNA 表达水平和表观遗传修饰。通过用 PKA 抑制剂 (H89)、丝裂原和应激激活激酶 1 (MSK1) 抑制剂 (SB-747651A) 或 forskolin处理来实现 AC/PKA 途径的药理学操作。24 和 48 小时 LPS 处理在选定的启动子上建立异染色质,对应于 mRNA 表达的减少。同时用 LPS 处理利培酮治疗既可以“阻断”又可以“逆转”异染色质形成。forskolin 处理导致异染色质类似的解体作用。相反,H89 或 MSK1 抑制 PKA 均阻断利培酮对 LPS 诱导的异染色质的“正常化”作用。我们的结果表明,利培酮可以解聚异染色质,沿 G 蛋白/AC/PKA 途径发挥此作用。这种方法还可用于研究单一或联合药物处理对人细胞染色质组装的功能结果。