Department of Pathology, University of California San Diego, La Jolla, CA, USA.
Department of Ophthalmology, University of California San Diego, La Jolla, CA, USA.
EMBO Mol Med. 2022 Jan 11;14(1):e14511. doi: 10.15252/emmm.202114511. Epub 2021 Nov 15.
In the course of our studies aiming to discover vascular bed-specific endothelial cell (EC) mitogens, we identified leukemia inhibitory factor (LIF) as a mitogen for bovine choroidal EC (BCE), although LIF has been mainly characterized as an EC growth inhibitor and an anti-angiogenic molecule. LIF stimulated growth of BCE while it inhibited, as previously reported, bovine aortic EC (BAE) growth. The JAK-STAT3 pathway mediated LIF actions in both BCE and BAE cells, but a caspase-independent proapoptotic signal mediated by cathepsins was triggered in BAE but not in BCE. LIF administration directly promoted activation of STAT3 and increased blood vessel density in mouse eyes. LIF also had protective effects on the choriocapillaris in a model of oxidative retinal injury. Analysis of available single-cell transcriptomic datasets shows strong expression of the specific LIF receptor in mouse and human choroidal EC. Our data suggest that LIF administration may be an innovative approach to prevent atrophy associated with AMD, through protection of the choriocapillaris.
在我们旨在发现血管床特异性内皮细胞 (EC) 有丝分裂原的研究过程中,我们发现白血病抑制因子 (LIF) 是牛脉络膜 EC (BCE) 的有丝分裂原,尽管 LIF 主要被表征为 EC 生长抑制剂和抗血管生成分子。LIF 刺激 BCE 生长,而如先前报道的那样,抑制牛主动脉 EC (BAE) 生长。JAK-STAT3 途径介导了 BCE 和 BAE 细胞中的 LIF 作用,但 caspase 非依赖性的组织蛋白酶介导的促凋亡信号在 BAE 中触发,但在 BCE 中未触发。LIF 的给药直接促进了 STAT3 的激活,并增加了小鼠眼睛中的血管密度。LIF 对氧化视网膜损伤模型中的脉络膜毛细血管也有保护作用。对现有单细胞转录组数据集的分析表明,特异性 LIF 受体在小鼠和人脉络膜 EC 中表达强烈。我们的数据表明,通过保护脉络膜毛细血管,LIF 的给药可能是预防与 AMD 相关的萎缩的一种创新方法。