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Gaillard, A.-L.

Publications and source records attributed to Gaillard, A.-L..

2 recordsLinked to original sources

Hormonal gene expression changes in the zebrafish caudal neurosecretory system under acute environmental challenges

The caudal neurosecretory system (CNSS) is a neuroendocrine complex, found only in fishes, suggested to be involved in osmoregulation and thermo-adaptation. Although being discovered 70 years ago, the CNSS has been understudied and its physiological significance remains poorly understood. The zebrafish (Danio rerio) is a well-established model organism for functional studies, yet, so far, the role of the CNSS has not really been investigated in this species. In the present study, we attempted to identify environmental factors whose variations induce changes in CNSS activity. Juvenile zebrafish were submitted to acute (2 h, 8 h, and 24 h) pH, salinity, and temperature challenges, and CNSS activity was quantified by measuring the expression levels of peptide hormone-encoding genes using quantitative PCR. Our findings revealed that temperature challenge affected the expression of the largest number of gene, followed by salinity and pH challenges. This suggested that, in the zebrafish, the CNSS is involved in thermo-adaptation and osmoregulation, which is consistent with what has been reported in other species, and showed that the zebrafish is a relevant model to study the function of the CNSS.

physiology↗

Urp1 and Urp2 act redundantly to maintain spine shape in zebrafish larvae.

Urp1 and Urp2 are two neuropeptides, members of the Urotensin 2 family, that have been recently involved in the control of body axis morphogenesis in zebrafish. They are produced by a population of sensory spinal neurons, called cerebrospinal fluid contacting neurons (CSF-cNs), under the control of signals relying on the Reissner fiber, an extracellular thread bathing in the CSF. Here, we have investigated further the function of Urp1 and Urp2 (Urp1/2) in body axis formation and maintenance. We showed that urp1;urp2 double mutants develop strong body axis defects during larval growth, revealing the redundancy between the two neuropeptides. These defects were similar to those previously reported in uts2r3 mutants. We observed that this phenotype is not associated with bone formation defects nor with increased inflammation status but, by using specific inhibitors, we found that the action of Urp1/2 depends on myosin II contraction. Finally, we provide evidence that while the Urp1/2 signaling is functioning during larval growth but is dispensable for embryonic development. Taken together, our results show that Urp1/2 signaling is required in larvae to promote correct vertebral body axis, most likely by regulating muscle tone.

developmental biology↗