Embryos extend their anterior-posterior (AP) axis in a conserved process known as axis elongation. Drosophila axis elongation occurs in an epithelial monolayer, the germband, and is driven by cell intercalation, cell shape changes, and oriented cell divisions at the posterior germband. Anterior germband cells also divide during axis elongation. We developed image analysis and pattern-recognition methods to track dividing cells from confocal microscopy movies in a generally applicable approach. Mesectoderm cells, forming the ventral midline, divided parallel to the AP axis, while lateral cells displayed a uniform distribution of division orientations. Mesectoderm cells did not intercalate and sustained increased AP strain before cell division. After division, mesectoderm cell density increased along the AP axis, thus relieving strain. We used laser ablation to isolate mesectoderm cells from the influence of other tissues. Uncoupling the mesectoderm from intercalating cells did not affect cell division orientation. Conversely, separating the mesectoderm from the anterior and posterior poles of the embryo resulted in uniformly oriented divisions. Our data suggest that mesectoderm cells align their division angle to reduce strain caused by mechanical forces along the AP axis of the embryo.
Transcriptional profiling has revealed a diverse range of cell states in cancer, but the function of these various states remains elusive. Using a combination of zebrafish melanoma modeling and human validation, we have identified a conserved stress-like state that confers intrinsic drug resistance and is associated with poor patient survival. Single cell sequencing of a series of transgenic zebrafish melanoma tumors revealed 3 distinct cell states that correspond to a neural crest, melanocyte or stress-like state. The existence of these 3 states was confirmed using spatial transcriptomics, a method that does not require tissue dissociation or cell sorting. The stress-like state expresses genes such as fos, hsp70 and ubb, proteins which are all required for adaptation to diverse cellular stresses. A transgenic reporter of the stress like state demonstrates that it has higher tumor seeding capabilities compared to non-stressed cells, and confers intrinsic resistance to MEK inhibitors, a commonly used melanoma therapeutic. The stress program can be induced by extrinsic processes such as heat shock, and confers resistance to MEK inhibitors in both zebrafish and human melanomas. Our study identifies a population of stress-like cells that are present from the time of tumor initiation, suggesting that the transcriptional seeds of therapeutic failure are established during the earliest steps of tumorigenesis. Citation Format: Maayan Baron, Mohita Tagore, Miranda Hunter, Isabella S. Kim, Reuben Moncada, Yun Yan, Nathaniel R. Campbell, Richard M. White, Itai Yanai. Cell state mapping reveals a role for a stress program in melanoma [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 1502.
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