Neural crest origin of sympathetic neurons at the dawn of vertebrates
Abstract
The neural crest is an embryonic stem cell population unique to vertebrates1 whose expansion and diversification are thought to have promoted vertebrate evolution by enabling emergence of new cell types and structures such as jaws and peripheral ganglia2. Although jawless vertebrates have sensory ganglia, convention has it that trunk sympathetic chain ganglia arose only in jawed vertebrates3,4,5,6,7,8. Here, by contrast, we report the presence of trunk sympathetic neurons in the sea lamprey, Petromyzon marinus, an extant jawless vertebrate. These neurons arise from sympathoblasts near the dorsal aorta that undergo noradrenergic specification through a transcriptional program homologous to that described in gnathostomes. Lamprey sympathoblasts populate the extracardiac space and extend along the length of the trunk in bilateral streams, expressing the catecholamine biosynthetic pathway enzymes tyrosine hydroxylase and dopamine β-hydroxylase. CM-DiI lineage tracing analysis further confirmed that these cells derive from the trunk neural crest. RNA sequencing of isolated ammocoete trunk sympathoblasts revealed gene profiles characteristic of sympathetic neuron function. Our findings challenge the prevailing dogma that posits that sympathetic ganglia are a gnathostome innovation, instead suggesting that a late-developing rudimentary sympathetic nervous system may have been characteristic of the earliest vertebrates.
Copyright and License
© The Author(s), under exclusive licence to Springer Nature Limited 2024.
Acknowledgement
We thank A. Collazo and G. Spigolon for microscopy training and assistance; I. Antoshechkin for discussion and assistance with library preparation and sequencing; G. Shin and N. Pierce for discussion and assistance with HCR probe design; and J. Stundlova, R. Fraser and D. Mayorga for lamprey husbandry. This work was supported by the grants NIH R35NS111564 to M.E.B., NIH F32HD106627 to B.M.E. and NIH F31DE031154 to H.A.U. J.S. is supported by a Marie Skłodowska-Curie grant, agreement no. 897949.
Contributions
The project was conceived of and designed by B.M.E. and M.E.B. Descriptive and transcriptomic analyses were carried out by B.M.E. CM-DiI labelling was carried out by J.S. and H.A.U. Preparation and sectioning of all T21 and T30 CM-DiI-labelled embryos was carried out by J.S. Lamprey husbandry and spawning were led by J.S. Writing and interpretation were carried out by B.M.E. and M.E.B. All authors approved the manuscript.
Data Availability
All raw RNA-sequencing data generated from this study are publicly available through the National Center for Biotechnology Information’s Gene Expression Omnibus database under the accession number GSE246248. RNA-sequencing data used for comparison to mouse sympathetic neurons were published previously41 and are available under the accession number GSE78845. Raw data can be made available upon request. Source data are provided with this paper.
Extended Data Fig. 1 Expression of sympathoadrenal genes at early embryonic stages.
Extended Data Fig. 3 Early expression of catecholamine biosynthetic enzymes.
Conflict of Interest
The authors declare no competing interests.
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Additional details
- ISSN
- 1476-4687
- URL
- https://rdcu.be/dE8z9
- National Institutes of Health
- R35NS111564
- National Institutes of Health
- NIH Postdoctoral Fellowship F32HD106627
- National Institutes of Health
- NIH Postdoctoral Fellowship F31DE031154
- European Research Council
- 897949 Marie Skłodowska-Curie Fellowship
- Caltech groups
- Division of Biology and Biological Engineering, Tianqiao and Chrissy Chen Institute for Neuroscience