Heather K Le Bleu, Rea G Kioussi, Astra L Henner, Victor M Lewis, Scott Stewart, Kryn Stankunas
{"title":"Voltage-gated calcium channels generate blastema Ca <sup>2+</sup> fluxes restraining zebrafish fin regenerative outgrowth.","authors":"Heather K Le Bleu, Rea G Kioussi, Astra L Henner, Victor M Lewis, Scott Stewart, Kryn Stankunas","doi":"10.1101/2024.08.21.608903","DOIUrl":null,"url":null,"abstract":"<p><p>Adult zebrafish fins regenerate to their original size regardless of damage extent, providing a tractable model of organ size and scale control. Gain-of-function of voltage-gated K <sup>+</sup> channels expressed in fibroblast-lineage blastema cells promotes excessive fin outgrowth, leading to a long-finned phenotype. Similarly, inhibition of the Ca <sup>2+</sup> -dependent phosphatase calcineurin during regeneration causes dramatic fin overgrowth. However, Ca <sup>2+</sup> fluxes and their potential origins from dynamic membrane voltages have not been explored or linked to fin size restoration. We used fibroblast-lineage GCaMP imaging of regenerating adult fins to identify widespread, heterogeneous Ca <sup>2+</sup> transients in distal blastema cells. Membrane depolarization of isolated regenerating fin fibroblasts triggered Ca <sup>2+</sup> spikes dependent on voltage-gated Ca <sup>2+</sup> channel activity. Single cell transcriptomics identified the voltage-gated Ca <sup>2+</sup> channels <i>cacna1c</i> (L-type channel), <i>cacna1ba</i> (N-type), and <i>cacna1g</i> (T-type) as candidate mediators of fibroblast-lineage Ca <sup>2+</sup> signaling. Small molecule inhibition revealed L- and/or N-type voltage-gated Ca <sup>2+</sup> channels act during regenerative outgrowth to restore fins to their original scale. Strikingly, <i>cacna1g</i> homozygous mutant zebrafish regenerated extraordinarily long fins due to prolonged outgrowth. The regenerated fins far exceeded their original length but with otherwise normal ray skeletons. Therefore, <i>cacna1g</i> mutants uniquely provide a genetic loss-of-function long-finned model that decouples developmental and regenerative fin outgrowth. Live GCaMP imaging of regenerating fins showed T-type Cacna1g channels enable Ca <sup>2+</sup> dynamics in distal fibroblast-lineage blastemal mesenchyme during the outgrowth phase. We conclude \"bioelectricity\" for fin size control likely entirely reflects voltage-modulated Ca <sup>2+</sup> dynamics in fibroblast-lineage blastemal cells that specifically and steadily decelerates outgrowth at a rate tuned to restore the original fin size.</p>","PeriodicalId":519960,"journal":{"name":"bioRxiv : the preprint server for biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11370486/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv : the preprint server for biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.21.608903","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Adult zebrafish fins regenerate to their original size regardless of damage extent, providing a tractable model of organ size and scale control. Gain-of-function of voltage-gated K + channels expressed in fibroblast-lineage blastema cells promotes excessive fin outgrowth, leading to a long-finned phenotype. Similarly, inhibition of the Ca 2+ -dependent phosphatase calcineurin during regeneration causes dramatic fin overgrowth. However, Ca 2+ fluxes and their potential origins from dynamic membrane voltages have not been explored or linked to fin size restoration. We used fibroblast-lineage GCaMP imaging of regenerating adult fins to identify widespread, heterogeneous Ca 2+ transients in distal blastema cells. Membrane depolarization of isolated regenerating fin fibroblasts triggered Ca 2+ spikes dependent on voltage-gated Ca 2+ channel activity. Single cell transcriptomics identified the voltage-gated Ca 2+ channels cacna1c (L-type channel), cacna1ba (N-type), and cacna1g (T-type) as candidate mediators of fibroblast-lineage Ca 2+ signaling. Small molecule inhibition revealed L- and/or N-type voltage-gated Ca 2+ channels act during regenerative outgrowth to restore fins to their original scale. Strikingly, cacna1g homozygous mutant zebrafish regenerated extraordinarily long fins due to prolonged outgrowth. The regenerated fins far exceeded their original length but with otherwise normal ray skeletons. Therefore, cacna1g mutants uniquely provide a genetic loss-of-function long-finned model that decouples developmental and regenerative fin outgrowth. Live GCaMP imaging of regenerating fins showed T-type Cacna1g channels enable Ca 2+ dynamics in distal fibroblast-lineage blastemal mesenchyme during the outgrowth phase. We conclude "bioelectricity" for fin size control likely entirely reflects voltage-modulated Ca 2+ dynamics in fibroblast-lineage blastemal cells that specifically and steadily decelerates outgrowth at a rate tuned to restore the original fin size.
成年斑马鱼的鳍能再生到原来的大小,而不受损伤程度的影响,这为器官大小和规模控制提供了一个可操作的模型。在成纤维细胞系胚芽细胞中表达的电压门控 K + 通道的功能增益会促进鳍的过度生长,从而导致长鳍表型。同样,在再生过程中抑制 Ca 2+ 依赖性磷酸酶钙调磷酸酶(calcineurin)也会导致鳍过度生长。然而,Ca 2+ 通量及其动态膜电压的潜在来源尚未被探索,也未与鳍的大小恢复联系起来。我们利用成纤维细胞系对再生成鳍的 GCaMP 成像来识别远端胚泡细胞中动态和异质的 Ca 2+ 瞬变。离体再生鳍成纤维细胞的膜去极化引发了依赖于电压门控 Ca 2+ 通道活性的 Ca 2+ 尖峰。单细胞转录组学发现电压门控 Ca 2+ 通道 cacna1c(L 型通道)、cacna1ba(N 型通道)和 cacna1g(T 型通道)是成纤维细胞线性 Ca 2+ 信号转导的候选介质。小分子抑制显示,L 型和/或 N 型电压门控 Ca 2+ 通道在再生生长过程中起作用,使鳍恢复到原来的大小。令人震惊的是,cacna1g 基因同源突变斑马鱼由于延长了鳍的生长时间,再生出了超长的鳍。再生的鳍远远超过了它们原来的长度,但鳍的骨骼却正常。因此,cacna1g 突变体提供了一个独特的遗传功能缺失长鳍模型,它能使发育和再生鳍的生长脱钩。再生鳍的实时 GCaMP 成像显示,T 型 Cacna1g 通道能在生长阶段使远端成纤维细胞系胚胎间充质中的 Ca 2+ 发生动态变化。我们的结论是,鳍大小控制的 "生物电 "可能完全反映了成纤维细胞期胚芽细胞中电压调制的 Ca 2+ 动态,这种动态特异且稳定地减慢了鳍的生长速度,从而恢复了鳍的原始大小。