Division of Genetic Medicine/Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Dev Biol. 2013 Nov 1;383(1):39-51. doi: 10.1016/j.ydbio.2013.08.027. Epub 2013 Sep 7.
Zebrafish gastrulation cell movements occur in the context of dynamic changes in extracellular matrix (ECM) organization and require the concerted action of planar cell polarity (PCP) proteins that regulate cell elongation and mediolateral alignment. Data obtained using Xenopus laevis gastrulae have shown that integrin-fibronectin interactions underlie the formation of polarized cell protrusions necessary for PCP and have implicated PCP proteins themselves as regulators of ECM. By contrast, the relationship between establishment of PCP and ECM assembly/remodeling during zebrafish gastrulation is unclear. We previously showed that zebrafish embryos carrying a null mutation in the four-pass transmembrane PCP protein vang-like 2 (vangl2) exhibit increased matrix metalloproteinase activity and decreased immunolabeling of fibronectin. These data implicated for the first time a core PCP protein in the regulation of pericellular proteolysis of ECM substrates and raised the question of whether other zebrafish PCP proteins also impact ECM organization. In Drosophila melanogaster, the cytoplasmic PCP protein Prickle binds Van Gogh and regulates its function. Here we report that similar to vangl2, loss of zebrafish prickle1a decreases fibronectin protein levels in gastrula embryos. We further show that Prickle1a physically binds Vangl2 and regulates both the subcellular distribution and total protein level of Vangl2. These data suggest that the ability of Prickle1a to impact fibronectin organization is at least partly due to effects on Vangl2. In contrast to loss of either Vangl2 or Prickle1a function, we find that glypican4 (a Wnt co-receptor) and frizzled7 mutant gastrula embryos with disrupted non-canonical Wnt signaling exhibit the opposite phenotype, namely increased fibronectin assembly. Our data show that glypican4 mutants do not have decreased proteolysis of ECM substrates, but instead have increased cell surface cadherin protein expression and increased intercellular adhesion. These data indicate that Wnt/Glypican4/Frizzled signaling regulates ECM assembly through effects on cadherin-mediated cell cohesion. Together, our results demonstrate that zebrafish Vangl2/Prickle1a and non-canonical Wnt/Frizzled signaling have opposing effects on ECM organization underlying PCP and gastrulation cell movements.
斑马鱼原肠胚细胞运动发生在外泌体基质(ECM)组织动态变化的背景下,需要平面细胞极性(PCP)蛋白的协同作用,这些蛋白调节细胞伸长和中侧对齐。使用非洲爪蟾原肠胚获得的数据表明,整合素-纤维连接蛋白相互作用是形成 PCP 所必需的极化细胞突起的基础,并暗示 PCP 蛋白本身是 ECM 的调节剂。相比之下,斑马鱼原肠胚中 PCP 的建立与 ECM 组装/重塑之间的关系尚不清楚。我们之前曾表明,携带四通道跨膜 PCP 蛋白vang-like 2(vangl2)缺失突变的斑马鱼胚胎表现出基质金属蛋白酶活性增加和纤维连接蛋白免疫标记减少。这些数据首次表明核心 PCP 蛋白参与 ECM 底物的细胞周蛋白酶解的调节,并提出了其他斑马鱼 PCP 蛋白是否也影响 ECM 组织的问题。在果蝇黑腹果蝇中,细胞质 PCP 蛋白 Prickle 与 Van Gogh 结合并调节其功能。在这里,我们报告说,类似于 vangl2,斑马鱼 prickle1a 的缺失降低了原肠胚胚胎中的纤维连接蛋白蛋白水平。我们进一步表明,Prickle1a 物理结合 Vangl2 并调节 Vangl2 的亚细胞分布和总蛋白水平。这些数据表明,Prickle1a 影响纤维连接蛋白组织的能力至少部分是由于对 Vangl2 的影响。与 Vangl2 或 Prickle1a 功能缺失相反,我们发现 Wnt 共受体 glypican4 和无 canonical Wnt 信号传导的 frizzled7 突变原肠胚胚胎表现出相反的表型,即纤维连接蛋白组装增加。我们的数据表明,glypican4 突变体没有 ECM 底物的蛋白水解减少,而是具有增加的细胞表面钙粘蛋白蛋白表达和增加的细胞间粘附。这些数据表明,Wnt/Glypican4/Frizzled 信号通过对钙粘蛋白介导的细胞粘着的影响调节 ECM 组装。总之,我们的结果表明,斑马鱼 Vangl2/Prickle1a 和非 canonical Wnt/Frizzled 信号对 PCP 和原肠胚细胞运动的 ECM 组织具有相反的影响。