» Articles » PMID: 25896280

Left-right Patterning in Xenopus Conjoined Twin Embryos Requires Serotonin Signaling and Gap Junctions

Overview
Journal Int J Dev Biol
Date 2015 Apr 22
PMID 25896280
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

A number of processes operating during the first cell cleavages enable the left-right (LR) axis to be consistently oriented during Xenopus laevis development. Prior work showed that secondary organizers induced in frog embryos after cleavage stages (i.e. conjoined twins arising from ectopic induced primary axes) correctly pattern their own LR axis only when a primary (early) organizer is also present. This instructive effect confirms the unique LR patterning functions that occur during early embryogenesis, but leaves open the question: which mechanisms that operate during early stages are also involved in the orientation of later-induced organizers? We sought to distinguish the two phases of LR patterning in secondary organizers (LR patterning of the primary twin and the later transfer of this information to the secondary twin) by perturbing only the latter process. Here, we used reagents that do not affect primary LR patterning at the time secondary organizers form to inhibit each of 4 mechanisms in the induced twin. Using pharmacological, molecular-genetic, and photo-chemical tools, we show that serotonergic and gap-junctional signaling, but not proton or potassium flows, are required for the secondary organizer to appropriately pattern its LR axis in a multicellular context. We also show that consistently-asymmetric gene expression begins prior to ciliary flow. Together, our data highlight the importance of physiological signaling in the propagation of cleavage-derived LR orientation to multicellular cell fields.

Citing Articles

Serotonin Inhibition of Claustrum Projection Neurons: Ionic Mechanism, Receptor Subtypes and Consequences for Claustrum Computation.

Wong K, Graf M, Augustine G Cells. 2024; 13(23).

PMID: 39682728 PMC: 11640313. DOI: 10.3390/cells13231980.


Integrating Bioelectrical Currents and Ca Signaling with Biochemical Signaling in Development and Pathogenesis.

Li A, Zhou J, Widelitz R, Chow R, Chuong C Bioelectricity. 2021; 2(3):210-220.

PMID: 34476353 PMC: 8370337. DOI: 10.1089/bioe.2020.0001.


First Evidence of Function for and RIOK-1.

Mughal M, Ye Q, Zhao L, Grevelding C, Li Y, Di W Pathogens. 2021; 10(7).

PMID: 34358012 PMC: 8308690. DOI: 10.3390/pathogens10070862.


Bioelectric signaling in regeneration: Mechanisms of ionic controls of growth and form.

McLaughlin K, Levin M Dev Biol. 2018; 433(2):177-189.

PMID: 29291972 PMC: 5753428. DOI: 10.1016/j.ydbio.2017.08.032.


Bioelectric gene and reaction networks: computational modelling of genetic, biochemical and bioelectrical dynamics in pattern regulation.

Pietak A, Levin M J R Soc Interface. 2017; 14(134).

PMID: 28954851 PMC: 5636277. DOI: 10.1098/rsif.2017.0425.


References
1.
Hyatt B, Yost H . The left-right coordinator: the role of Vg1 in organizing left-right axis formation. Cell. 1998; 93(1):37-46. DOI: 10.1016/s0092-8674(00)81144-7. View

2.
Vandenberg L, Lemire J, Levin M . Serotonin has early, cilia-independent roles in Xenopus left-right patterning. Dis Model Mech. 2012; 6(1):261-8. PMC: 3529356. DOI: 10.1242/dmm.010256. View

3.
Lobikin M, Wang G, Xu J, Hsieh Y, Chuang C, Lemire J . Early, nonciliary role for microtubule proteins in left-right patterning is conserved across kingdoms. Proc Natl Acad Sci U S A. 2012; 109(31):12586-91. PMC: 3412009. DOI: 10.1073/pnas.1202659109. View

4.
Danos M, Yost H . Linkage of cardiac left-right asymmetry and dorsal-anterior development in Xenopus. Development. 1995; 121(5):1467-74. DOI: 10.1242/dev.121.5.1467. View

5.
Klar A . A model for specification of the left-right axis in vertebrates. Trends Genet. 1994; 10(11):392-6. DOI: 10.1016/0168-9525(94)90055-8. View