Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, CA 93106, USA
Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, CA 93106, USA.
Development. 2020 Aug 7;147(15):dev184663. doi: 10.1242/dev.184663.
The colonial ascidian regenerates the germline during repeated cycles of asexual reproduction. Germline stem cells (GSCs) circulate in the blood and migrate to new germline niches as they develop and this homing process is directed by a Sphigosine-1-Phosphate (S1P) gradient. Here, we find that inhibition of ABC transporter activity reduces migration of GSCs towards low concentrations of S1P In addition, inhibiting phospholipase A2 (PLA2) or lipoxygenase (Lox) blocks chemotaxis towards low concentrations of S1P. These effects can be rescued by addition of the 12-Lox product 12-S-HETE. Blocking ABC transporter, PLA2 or 12-Lox activity also inhibits homing of germ cells Using a live-imaging chemotaxis assay in a 3D matrix, we show that a shallow gradient of 12-S-HETE enhances chemotaxis towards low concentrations of S1P and stimulates motility. A potential homolog of the human receptor for 12-S-HETE, , is expressed on GSCs and differentiating germ cells. These results suggest that 12-S-HETE might be an autocrine signaling molecule exported by ABC transporters that enhances chemotaxis in GSCs migrating towards low concentrations of S1P.
殖民性海鞘在无性繁殖的反复循环中再生生殖线。生殖干细胞 (GSCs) 在血液中循环,并在发育过程中迁移到新的生殖线龛位,这个归巢过程由 Sphigosine-1-Phosphate (S1P) 梯度指导。在这里,我们发现抑制 ABC 转运体的活性会减少 GSCs 向低浓度 S1P 的迁移。此外,抑制磷脂酶 A2 (PLA2) 或脂氧合酶 (Lox) 会阻止向低浓度 S1P 的趋化作用。通过添加 12-Lox 产物 12-S-HETE 可以挽救这些效应。抑制 ABC 转运体、PLA2 或 12-Lox 的活性也会抑制生殖细胞的归巢。通过在 3D 基质中进行实时成像趋化性测定,我们表明 12-S-HETE 的浅梯度增强了对低浓度 S1P 的趋化性,并刺激了运动性。人类 12-S-HETE 受体的潜在同源物 在 GSCs 和分化的生殖细胞上表达。这些结果表明,12-S-HETE 可能是一种由 ABC 转运体输出的自分泌信号分子,可增强向低浓度 S1P 迁移的 GSCs 的趋化性。