Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (A.T., S.H., H.S.C., D.P.-C., M.A.H., A.J., S.A.S., M.A., P.B.Y., M.W.F., J.P.).
Harvard Medical School, Boston, MA (A.T., S.H., H.S.C., D.P.-C., M.A.H., A.J., S.A.S., M.A., P.B.Y., T.W., Y.S., M.W.F., J.P.).
Arterioscler Thromb Vasc Biol. 2024 Jan;44(1):143-155. doi: 10.1161/ATVBAHA.123.319909. Epub 2023 Nov 9.
BETs (bromodomain and extraterminal domain-containing epigenetic reader proteins), including BRD4 (bromodomain-containing protein 4), orchestrate transcriptional programs induced by pathogenic stimuli, as intensively studied in cardiovascular disease and elsewhere. In endothelial cells (ECs), BRD4 directs induced proinflammatory, proatherosclerotic transcriptional responses; BET inhibitors, like JQ1, repress these effects and decrease atherosclerosis. While BET effects in pathogenic conditions have prompted therapeutic BET inhibitor development, BET action under basal conditions, including ECs, has remained understudied. To understand BET action in basal endothelial transcriptional programs, we first analyzed EC RNA-Seq data in the absence versus presence of JQ1 before using BET regulation to identify novel determinants of EC biology and function.
RNA-Seq datasets of human umbilical vein ECs without and with JQ1 treatment were analyzed. After identifying C12orf34, also known as FAM222A (family with sequence similarity 222 member A), as a previously unreported, basally expressed, potently JQ1-induced EC gene, FAM222A was studied in endothelial and angiogenic responses in vitro using small-interference RNA silencing and lentiviral overexpression, in vitro, ex vivo and in vivo, including aortic sprouting, matrigel plug assays, and murine neonatal oxygen-induced retinopathy.
Resting EC RNA-Seq data indicate BETs direct transcriptional programs underlying core endothelial properties including migration, proliferation, and angiogenesis. BET inhibition in resting ECs also significantly induced a subset of mRNAs, including FAM222A-a unique BRD4-regulated gene with no reported EC role. Silencing endothelial FAM222A significantly decreased cellular proliferation, migration, network formation, aorta sprouting, and Matrigel plug vascularization through coordinated modulation of VEGF (vascular endothelial growth factor) and NOTCH mediator expression in vitro, ex vivo, in vivo; lentiviral FAM222A overexpression had opposite effects. In vivo, siFAM222A significantly repressed retinal revascularization in neonatal murine oxygen-induced retinopathy through similar angiogenic signaling modulation.
BET control over the basal endothelial transcriptome includes FAM222A, a novel, BRD4-regulated, key determinant of endothelial biology and angiogenesis.
BETs(溴结构域和末端结构域包含的表观遗传读取蛋白),包括 BRD4(含溴结构域蛋白 4),在心血管疾病和其他地方的致病性刺激诱导的转录程序中发挥协调作用。在血管内皮细胞(ECs)中,BRD4 指导诱导的促炎、促动脉粥样硬化的转录反应;BET 抑制剂,如 JQ1,抑制这些作用并减少动脉粥样硬化。虽然 BET 在致病条件下的作用促使了治疗性 BET 抑制剂的开发,但包括 ECs 在内的基础条件下 BET 的作用仍未得到充分研究。为了了解 BET 在基础内皮转录程序中的作用,我们首先分析了没有和有 JQ1 处理的人脐静脉 ECs 的 RNA-Seq 数据,然后利用 BET 调节来鉴定新的 EC 生物学和功能决定因素。
分析了没有和有 JQ1 处理的人脐静脉 ECs 的 RNA-Seq 数据集。在鉴定出 C12orf34(也称为 FAM222A(家族与序列相似性 222 成员 A))作为一个以前未报道的、基础表达的、强烈的 JQ1 诱导的 EC 基因后,使用小干扰 RNA 沉默和慢病毒过表达,在体外、离体和体内研究了 FAM222A 在血管生成反应中的作用,包括主动脉发芽、基质胶塞实验和小鼠新生氧诱导的视网膜病变。
静止期 EC 的 RNA-Seq 数据表明,BETs 指导着核心内皮特性的转录程序,包括迁移、增殖和血管生成。静止期 EC 中的 BET 抑制也显著诱导了一组 mRNA,包括 FAM222A-一个独特的 BRD4 调节基因,没有报道的 EC 作用。沉默内皮细胞中的 FAM222A 通过协调调节 VEGF(血管内皮生长因子)和 NOTCH 调节剂的表达,显著降低了细胞增殖、迁移、网络形成、主动脉发芽和基质胶塞血管生成,体外、离体、体内;慢病毒过表达 FAM222A 则有相反的效果。在体内,siFAM222A 通过类似的血管生成信号调节,显著抑制了新生氧诱导的视网膜病变中的视网膜新生血管化。
BET 对基础内皮转录组的控制包括 FAM222A,这是一个新的、BRD4 调节的、内皮生物学和血管生成的关键决定因素。