Neural crest cells are a highly migratory pluripotent cell population that generates a wide array of different cell types and failure in their migration can result in severe birth defects and malformation syndromes. Neural crest migration is controlled by various means including chemotaxis, repellent guidance cues and cell-cell interaction. Non-canonical Wnt PCP (planar cell polarity) signaling has previously been shown to control cell-contact mediated neural crest cell guidance. PTK7 (protein tyrosine kinase 7) is a transmembrane pseudokinase and a known regulator of Wnt/PCP signaling, which is expressed in Xenopus neural crest cells and required for their migration. PTK7 functions as a Wnt co-receptor; however, it remains unclear by which means PTK7 affects neural crest migration. Expressing fluorescently labeled proteins in Xenopus neural crest cells we find that PTK7 co-localizes with the Ror2 Wnt-receptor. Further, co-immunoprecipitation experiments demonstrate that PTK7 interacts with Ror2. The PTK7/Ror2 interaction is likely relevant for neural crest migration, because Ror2 expression can rescue the PTK7 loss of function migration defect. Live cell imaging of explanted neural crest cells shows that PTK7 loss of function affects the formation of cell protrusions as well as cell motility. Co-expression of Ror2 can rescue these defects. In vivo analysis demonstrates that a kinase dead Ror2 mutant cannot rescue PTK7 loss of function. Thus, our data suggest that Ror2 can substitute for PTK7 and that the signaling function of its kinase domain is required for this effect.
Oxygen consumption allows measuring the metabolic activity of organisms. Here, we adopted the multi-well plate-based respirometry of the extracellular flux analyzer (Seahorse XF96) to investigate the effect of temperature on the bioenergetics of zebrafish embryos (Danio rerio) in situ. We show that the removal of the embryonic chorion is beneficial for oxygen consumption rates (OCR) and penetration of various mitochondrial inhibitors, and confirm that sedation reduces the variability of OCR. At 48h post-fertilization, embryos (maintained at a routine temperature of 28°C) were exposed to different medium temperatures ranging from 18°C to 37°C for 20h prior OCR measurement. Measurement temperatures from 18°C to 45°C in the XF96 were achieved by lowering the room temperature and active in-built heating. At 18°C assay temperature, basal OCR was low due to decreased ATP-linked respiration, which was not limited by mitochondrial power, as seen in substantial spare respiratory capacity. Basal OCR of the embryos increased with assay temperature and were stable up to 37°C assay temperature, with pre-exposure of 37°C resulting in more thermo-resistant basal OCR measured at 41°C. Adverse effects of the mitochondrial inhibitor oligomycin were seen at 37°C and chemical uncouplers disrupted substrate oxidation gradually with increasing assay temperature. Proton leak respiration increased at assay temperatures above 28°C and compromised the efficiency of ATP production, calculated as coupling efficiency. Thus, temperature impacts mitochondrial respiration by reduced cellular ATP turnover at lower temperatures and by increased proton leak at higher temperatures. This conclusion is coherent with the assessment of heart rate, an independent indicator of systemic metabolic rate, which increased with exposure temperature, peaking at 28°C, and decreased at higher temperatures. Collectively, plate-based respirometry allows assessing distinct parts of mitochondrial energy transduction in zebrafish embryos and investigating the effect of temperature and temperature acclimation on mitochondrial bioenergetics in situ.
No abstract
All species require bioenergetic adaptation to maintain life functions, especially in changing environmental conditions. Global warming and deteriorating water quality may pose threats to aquatic species by interfering with bioenergetic mechanisms. Mitochondrial oxidative metabolism is a key component for bioenergetic responses as it provides the major proportion of cellular energy in the form of adenosine triphosphate (ATP). In our studies, we aim to establish the assessment of zebrafish mitochondrial bioenergetics and investigate the mechanisms, adaptation, and plasticity to temperature, pollutants, and the combination of both to gain insights into the upcoming threats for their energy homeostasis and survival. Using plate‐based respirometry of the Seahorse XF96 analyzer, we measured zebrafish (Danio rerio) embryo oxygen consumption rates in situ. To understand how temperature alters oxidative phosphorylation, we exposed 48 hours post‐fertilization zebrafish embryos to five different water temperatures before measuring oxygen consumption at various assay temperatures. The oxygen consumption rates were challenged using respiratory chain inhibitors and chemical uncouplers to reveal bioenergetic mechanisms and adjustments of mitochondrial efficiency. We show that at 18°C assay temperature, basal oxygen consumption of the embryo is low due to decreased ATP‐linked respiration and not limited by maximum substrate oxidation. Basal oxygen consumption rates increase with assay temperature and remain stable up to 37°C, before rapidly deteriorating at 41°C and above. The pre‐exposure of embryos to 37°C, however, expands the thermal window to higher limits, indicated by stable basal oxygen consumption rates at 41°C. Proton leak respiration, which wastes nutrient energy in parallel to ATP production, increases at assay temperatures above 28°C, thereby reducing the efficiency of ATP synthesis. This is seen as a decrease in coupling efficiency, which is defined as the fraction of oxygen consumption that drives ATP synthesis. Collectively, temperature affects the performance of zebrafish embryos by reducing cellular ATP turnover at lower temperatures and by increasing proton leak at higher temperatures, resulting in an optimum energy conversion temperature that can be shifted by thermal adaptation. In current experiments, we measure how pollutants impact zebrafish bioenergetics and its relation to thermal adaptation.
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