Evidence that ABC-transporter-mediated autocrine export of an eicosanoid signaling molecule enhances germ cell chemotaxis in the colonial tunicate Botryllus schlosseri
Autor: | Anthony W. De Tomaso, Delany Rodriguez, Susannah H. Kassmer |
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Rok vydání: | 2020 |
Předmět: |
0303 health sciences
biology fungi ATP-binding cassette transporter Chemotaxis Botryllus schlosseri biology.organism_classification Germline Cell biology 03 medical and health sciences 0302 clinical medicine medicine.anatomical_structure 030220 oncology & carcinogenesis medicine lipids (amino acids peptides and proteins) Autocrine signalling Molecular Biology Germ cell 030304 developmental biology Developmental Biology Chemotaxis assay Homing (hematopoietic) |
Zdroj: | Development. |
ISSN: | 1477-9129 0950-1991 |
DOI: | 10.1242/dev.184663 |
Popis: | The colonial ascidian Botryllus schlosseri 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 vitro. 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 in vivo. 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, gpr31, is expressed on GSCs and differentiating vasa+ 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. |
Databáze: | OpenAIRE |
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