Hick Anne-Christine, van Eyll Jonathan M, Cordi Sabine, Forez Céline, Passante Lara, Kohara Hiroshi, Nagasawa Takashi, Vanderhaeghen Pierre, Courtoy Pierre J, Rousseau Guy G, Lemaigre Frédéric P, Pierreux Christophe E
Université catholique de Louvain, de Duve Institute, Brussels, Belgium.
BMC Dev Biol. 2009 Dec 14;9:66. doi: 10.1186/1471-213X-9-66.
The exocrine pancreas is composed of a branched network of ducts connected to acini. They are lined by a monolayered epithelium that derives from the endoderm and is surrounded by mesoderm-derived mesenchyme. The morphogenic mechanisms by which the ductal network is established as well as the signaling pathways involved in this process are poorly understood.
By morphological analyzis of wild-type and mutant mouse embryos and using cultured embryonic explants we investigated how epithelial morphogenesis takes place and is regulated by chemokine signaling. Pancreas ontogenesis displayed a sequence of two opposite epithelial transitions. During the first transition, the monolayered and polarized endodermal cells give rise to tissue buds composed of a mass of non polarized epithelial cells. During the second transition the buds reorganize into branched and polarized epithelial monolayers that further differentiate into tubulo-acinar glands. We found that the second epithelial transition is controlled by the chemokine Stromal cell-Derived Factor (SDF)-1. The latter is expressed by the mesenchyme, whereas its receptor CXCR4 is expressed by the epithelium. Reorganization of cultured pancreatic buds into monolayered epithelia was blocked in the presence of AMD3100, a SDF-1 antagonist. Analyzis of sdf1 and cxcr4 knockout embryos at the stage of the second epithelial transition revealed transient defective morphogenesis of the ventral and dorsal pancreas. Reorganization of a globular mass of epithelial cells in polarized monolayers is also observed during submandibular glands development. We found that SDF-1 and CXCR4 are expressed in this organ and that AMD3100 treatment of submandibular gland explants blocks its branching morphogenesis.
In conclusion, our data show that the primitive pancreatic ductal network, which is lined by a monolayered and polarized epithelium, forms by remodeling of a globular mass of non polarized epithelial cells. Our data also suggest that SDF-1 controls the branching morphogenesis of several exocrine tissues.
外分泌胰腺由与腺泡相连的分支导管网络组成。它们由单层上皮细胞衬里,该上皮细胞起源于内胚层,并被中胚层衍生的间充质所包围。导管网络建立的形态发生机制以及该过程中涉及的信号通路尚不清楚。
通过对野生型和突变小鼠胚胎的形态学分析以及使用培养的胚胎外植体,我们研究了上皮形态发生如何发生以及受趋化因子信号传导的调控。胰腺发生表现出两个相反上皮转变的序列。在第一次转变期间,单层极化的内胚层细胞产生由大量非极化上皮细胞组成的组织芽。在第二次转变期间,芽重新组织成分支状和极化的上皮单层,进一步分化为管状腺泡腺。我们发现第二次上皮转变受趋化因子基质细胞衍生因子(SDF)-1控制。后者由间充质表达,而其受体CXCR4由上皮表达。在SDF-1拮抗剂AMD3100存在下,培养的胰腺芽重组为单层上皮被阻断。在第二次上皮转变阶段对sdf1和cxcr4基因敲除胚胎的分析显示腹侧和背侧胰腺存在短暂的形态发生缺陷。在颌下腺发育过程中也观察到上皮细胞球状团块重组为极化单层。我们发现SDF-1和CXCR4在该器官中表达,并且AMD3100处理颌下腺外植体可阻断其分支形态发生。
总之,我们的数据表明,由单层极化上皮衬里的原始胰腺导管网络是通过非极化上皮细胞球状团块的重塑形成的。我们的数据还表明SDF-1控制几种外分泌组织的分支形态发生。