Department of Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida School of Medicine, Tampa, Florida.
Department of Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida School of Medicine, Tampa, Florida.
Am J Pathol. 2024 Apr;194(4):574-598. doi: 10.1016/j.ajpath.2023.08.017. Epub 2023 Oct 12.
This study sought to define key molecules and signals controlling major steps in vascular morphogenesis, and how these signals regulate pericyte recruitment and pericyte-induced basement membrane deposition. The morphogenic impact of endothelial cell (EC) expression of activating mutants of Kirsten rat sarcoma virus (kRas), mitogen-activated protein kinase 1 (Mek1), phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA), Akt serine/threonine kinase 1 (Akt1), Ras homolog enriched in brain (Rheb) Janus kinase 2 (Jak2), or signal transducer and activator of transcription 3 (Stat3) expression versus controls was evaluated, along with EC signaling events, pharmacologic inhibitor assays, and siRNA suppression experiments. Primary stimulators of EC lumen formation included kRas, Akt1, and Mek1, whereas PIK3CA and Akt1 stimulated a specialized type of cystic lumen formation. In contrast, the key drivers of EC sprouting behavior were Jak2, Stat3, Mek1, PIK3CA, and mammalian target of rapamycin (mTor). These conclusions are further supported by pharmacologic inhibitor and siRNA suppression experiments. EC expression of active Akt1, kRas, and PIK3CA led to markedly dysregulated lumen formation coupled to strongly inhibited pericyte recruitment and basement membrane deposition. For example, activated Akt1 expression in ECs excessively stimulated lumen formation, decreased EC sprouting behavior, and showed minimal pericyte recruitment with reduced mRNA expression of platelet-derived growth factor-BB, platelet-derived growth factor-DD, and endothelin-1, critical EC-derived factors known to stimulate pericyte invasion. The study identified key signals controlling fundamental steps in capillary morphogenesis and maturation and provided mechanistic details on why EC activating mutations induced a capillary deficiency state with abnormal lumens, impaired pericyte recruitment, and basement deposition: predisposing stimuli for the development of vascular malformations.
这项研究旨在确定控制血管形态发生主要步骤的关键分子和信号,以及这些信号如何调节周细胞募集和周细胞诱导的基底膜沉积。评估了内皮细胞 (EC) 表达激活型 Kirsten 大鼠肉瘤病毒 (kRas)、丝裂原活化蛋白激酶 1 (Mek1)、磷脂酰肌醇-4,5-二磷酸 3-激酶催化亚单位 α (PIK3CA)、Akt 丝氨酸/苏氨酸激酶 1 (Akt1)、 Ras 同源物富集于脑 (Rheb) Janus 激酶 2 (Jak2) 或信号转导和转录激活因子 3 (Stat3) 表达相对于对照的形态发生影响,以及 EC 信号事件、药理抑制剂测定和 siRNA 抑制实验。kRas、Akt1 和 Mek1 是初级刺激物,促进 EC 管腔形成,而 PIK3CA 和 Akt1 则刺激特殊类型的囊性管腔形成。相反,EC 发芽行为的关键驱动因素是 Jak2、Stat3、Mek1、PIK3CA 和哺乳动物雷帕霉素靶蛋白 (mTor)。这些结论得到了药理抑制剂和 siRNA 抑制实验的进一步支持。EC 中活性 Akt1、kRas 和 PIK3CA 的表达导致明显失调的管腔形成,同时强烈抑制周细胞募集和基底膜沉积。例如,EC 中激活的 Akt1 表达过度刺激管腔形成,减少 EC 发芽行为,并显示出最小的周细胞募集,同时血小板衍生生长因子-BB、血小板衍生生长因子-DD 和内皮素-1 的 mRNA 表达减少,这些是已知刺激周细胞侵袭的关键 EC 衍生因子。该研究确定了控制毛细血管形态发生和成熟基本步骤的关键信号,并提供了机制细节,说明为什么 EC 激活突变导致毛细血管缺陷状态,具有异常管腔、受损的周细胞募集和基底沉积:这是血管畸形发展的倾向性刺激因素。