Department of Pediatrics, Section of Developmental Biology School of Medicine Aurora, University of Colorado, CO 80045.
eNeuro. 2017 May 26;4(3). doi: 10.1523/ENEURO.0378-16.2017. eCollection 2017 May-Jun.
The blood-brain barrier (BBB) is a multifaceted property of the brain vasculature that protects the brain and maintains homeostasis by tightly regulating the flux of ions, molecules, and cells across the vasculature. Blood vessels in the brain are formed by endothelial cells that acquire barrier properties, such as tight and adherens junctions, soon after the brain vasculature is formed. Endothelial WNT signaling is crucial to induce these BBB properties by regulating their expression and stabilization. Recent studies have implicated retinoic acid (RA) signaling in BBB development and shown that pharmacological concentrations of RA (≥5 µm) can induce BBB properties in cultured brain endothelial cells. However, a recent study demonstrated that RA inhibits endothelial WNT signaling during brain development, suggesting that RA does not promote BBB properties. We therefore investigated whether RA plays a physiological role in BBB development. We found that BBB function and junctional protein expression was unaffected in mouse mutants that have a reduced capacity to synthesize RA ( mutants). Furthermore, embryos exposed to a RA-enriched diet did not enhance BBB protein expression. Together, our data indicate that RA is not capable of inducing, nor is it required for, BBB protein expression . Like other studies, we found that pharmacological concentrations of RA induce BBB genes in cultured murine brain endothelial cells, and this may involve activation of the LXR/RXR signaling pathway. Our data do not support a role for RA in BBB development, but confirm reports that pharmacological RA is a robust tool to induce BBB properties in culture.
血脑屏障(BBB)是脑血管的一种多方面特性,通过紧密调节离子、分子和细胞穿过血管的通量来保护大脑并维持体内平衡。大脑中的血管由内皮细胞形成,这些内皮细胞在脑血管形成后不久就获得了屏障特性,如紧密连接和黏附连接。内皮细胞 WNT 信号对于通过调节其表达和稳定性来诱导这些 BBB 特性至关重要。最近的研究表明,视黄酸(RA)信号在 BBB 发育中起作用,并表明药理浓度的 RA(≥5 µm)可以在培养的脑内皮细胞中诱导 BBB 特性。然而,最近的一项研究表明,RA 在大脑发育过程中抑制内皮细胞 WNT 信号,表明 RA 不会促进 BBB 特性。因此,我们研究了 RA 是否在 BBB 发育中发挥生理作用。我们发现,在合成 RA 能力降低的小鼠突变体(突变体)中,BBB 功能和连接蛋白表达不受影响。此外,暴露于富含 RA 的饮食中的胚胎并未增强 BBB 蛋白表达。总之,我们的数据表明 RA 既不能诱导 BBB 蛋白表达,也不需要 BBB 蛋白表达。与其他研究一样,我们发现药理浓度的 RA 诱导培养的鼠脑内皮细胞中 BBB 基因的表达,这可能涉及 LXR/RXR 信号通路的激活。我们的数据不支持 RA 在 BBB 发育中的作用,但证实了药理 RA 是在培养物中诱导 BBB 特性的有力工具的报道。