Lim Kah Jing, Brandt William D, Heth Jason A, Muraszko Karin M, Fan Xing, Bar Eli E, Eberhart Charles G
Department of Pathology, Johns Hopkins University, Baltimore, MD 21231, Maryland, USA.
Department of Neurosurgery, University of Michigan, Ann Arbor, MI 48109, Michigan, USA.
Oncotarget. 2015 Jan 30;6(3):1666-77. doi: 10.18632/oncotarget.2762.
During normal development, heterogeneous expression of Notch ligands can result in pathway suppression in the signal-sending cell, a process known as lateral inhibition. It is unclear if an analogous phenomenon occurs in malignant cells. We observed significant induction of Notch ligands in glioblastoma neurospheres and pancreatic carcinoma cells cultured in low oxygen, suggesting that this phenomenon could occur around hypoxic regions. To model lateral inhibition in these tumors, the ligand Jagged1 was overexpressed in glioblastoma and pancreatic carcinoma cells, resulting in overall induction of pathway targets. However, when ligand high and ligand low cells from a single line were co-cultured and then separated, we noted suppression of Notch pathway targets in the former and induction in the latter, suggesting that neoplastic lateral inhibition can occur. We also found that repression of Notch pathway targets in signal-sending cells may occur through the activity of a Notch ligand intracellular domain, which translocates into the nucleus. Understanding how this neoplastic lateral inhibition process functions in cancer cells may be important in targeting ligand driven Notch signaling in solid tumors.
在正常发育过程中,Notch配体的异质性表达可导致信号发送细胞中的信号通路受到抑制,这一过程称为侧向抑制。目前尚不清楚恶性细胞中是否会出现类似现象。我们观察到,在低氧条件下培养的胶质母细胞瘤神经球和胰腺癌细胞中,Notch配体有显著诱导,这表明这种现象可能发生在缺氧区域周围。为了模拟这些肿瘤中的侧向抑制,在胶质母细胞瘤和胰腺癌细胞中过表达配体Jagged1,导致信号通路靶点的整体诱导。然而,当将来自同一细胞系的配体高表达和配体低表达细胞共培养然后分离时,我们注意到前者中Notch信号通路靶点受到抑制,而后者中则被诱导,这表明肿瘤性侧向抑制可能会发生。我们还发现,信号发送细胞中Notch信号通路靶点的抑制可能是通过Notch配体细胞内结构域的活性发生的,该结构域会转移到细胞核中。了解这种肿瘤性侧向抑制过程在癌细胞中如何发挥作用,对于靶向实体瘤中配体驱动的Notch信号传导可能具有重要意义。