Angelo Jesse R, Tremblay Kimberly D
Department of Veterinary&Animal Sciences, University of Massachusetts, Amherst, MA, USA.
Department of Veterinary&Animal Sciences, University of Massachusetts, Amherst, MA, USA.
Dev Biol. 2018 Mar 1;435(1):15-25. doi: 10.1016/j.ydbio.2018.01.003. Epub 2018 Jan 9.
The murine pancreas buds from the ventral embryonic endoderm at approximately 8.75 dpc and a second pancreas bud emerges from the dorsal endoderm by 9.0 dpc. Although it is clear that secreted signals from adjacent mesoderm-derived sources are required for both the appropriate emergence and further refinement of the pancreatic endoderm, neither the exact signals nor the requisite tissue sources have been defined in mammalian systems. Herein we use DiI fate mapping of cultured murine embryos to identify the embryonic sources of both the early inductive and later condensed pancreatic mesenchyme. Despite being capable of supporting pancreas induction from dorsal endoderm in co-culture experiments, we find that in the context of the developing embryo, the dorsal aortae as well as the paraxial, intermediate, and lateral mesoderm derivatives only transiently associate with the dorsal pancreas bud, producing descendants that are decidedly anterior to the pancreas bud. Unlike these other mesoderm derivatives, the axial (notochord) descendants maintain association with the dorsal pre-pancreatic endoderm and early pancreas bud. This fate mapping data points to the notochord as the likely inductive source in vivo while also revealing dynamic morphogenetic movements displayed by individual mesodermal subtypes. Because none of the mesoderm examined above produced the pancreatic mesenchyme that condenses around the induced bud to support exocrine and endocrine differentiation, we also sought to identify the mesodermal origins of this mesenchyme. We identify a portion of the coelomic mesoderm that contributes to the condensed pancreatic mesenchyme. In conclusion, we identify a portion of the notochord as a likely source of the signals required to induce and maintain the early dorsal pancreas bud, demonstrate that the coelomic mesothelium contributes to the dorsal and ventral pancreatic mesenchyme, and provide insight into the dynamic morphological rearrangements of mesoderm-derived tissues during early organogenesis stages of mammalian development.
小鼠胰腺在大约胚胎发育8.75天从腹侧胚胎内胚层出芽,第二个胰腺芽在胚胎发育9.0天从背侧内胚层出现。虽然很明显,来自相邻中胚层来源的分泌信号对于胰腺内胚层的适当出现和进一步细化是必需的,但在哺乳动物系统中,确切的信号和必需的组织来源都尚未明确。在此,我们使用培养的小鼠胚胎的DiI命运图谱来确定早期诱导性和后期凝聚性胰腺间充质的胚胎来源。尽管在共培养实验中能够支持背侧内胚层的胰腺诱导,但我们发现,在发育中的胚胎环境中,背主动脉以及轴旁、中间和外侧中胚层衍生物仅与背侧胰腺芽短暂关联,产生的后代明显位于胰腺芽的前方。与这些其他中胚层衍生物不同,轴(脊索)的后代与背侧胰腺前内胚层和早期胰腺芽保持关联。这种命运图谱数据表明脊索可能是体内的诱导源,同时也揭示了各个中胚层亚型所展示的动态形态发生运动。由于上述检查的中胚层均未产生围绕诱导芽凝聚以支持外分泌和内分泌分化的胰腺间充质,我们还试图确定这种间充质的中胚层起源。我们确定了一部分体腔中胚层对凝聚性胰腺间充质有贡献。总之,我们确定了一部分脊索是诱导和维持早期背侧胰腺芽所需信号的可能来源,证明体腔间皮对背侧和腹侧胰腺间充质有贡献,并深入了解了哺乳动物发育早期器官发生阶段中胚层来源组织的动态形态重排。