# A Subset of Circulating Hemocytes Expresses Genes Indicating Neural Precursor Identity

**Authors:** Thanapong Kruangkum, Kenneth Söderhäll, Irene Söderhäll

PMC · DOI: 10.1007/s10571-026-01686-x · Cellular and Molecular Neurobiology · 2026-02-09

## TL;DR

A small percentage of blood cells in crayfish express genes linked to neural development, suggesting they may act as neural precursors in adult neurogenesis.

## Contribution

First demonstration that neural lineage markers are expressed in a distinct population of crustacean hemocytes.

## Key findings

- Around 1% of circulating hemocytes express neural lineage marker transcripts.
- Neural marker transcripts co-express with serotonin receptor 1 in some hemocytes.
- Treatments like serotonin and brain injury increase the proportion of neural marker-positive hemocytes.

## Abstract

Adult neurogenesis in crayfish has been shown to require progenitors from an external source linked with the hematopoietic system, and some hemocyte (blood cell) types are attracted to a neurogenic niche in the brain. By using multiplex RNA-FISH techniques we have for the first time detected specific neural lineage marker transcripts expressed together in a small proportion of the circulating hemocytes (around 1%). This finding agrees with and confirms that there is only a small proportion of hemocytes which can develop further into neurons. Interestingly, these transcripts were co-expressed in the same cell as well as sometimes together with the transcript of the serotonin receptor 1 (5htr1+). Moreover, we could also show that several treatments, including serotonin, astakine, and lipopolysaccharide, as well as an acute brain injury, could induce a greater proportion of such neural marker positive hemocytes in the circulation as a response to these stimuli. Cells expressing neural lineage marker transcripts were also detected in the HPT, the hemocyte producing organ. Such neural lineage marker positive cells were shown to be present in the hemocyte-associated vascular plexus and the perineurial glia-like cells of the brain. These findings, therefore, for the first time demonstrate that the neural lineage markers are expressed in a distinct population of crustacean hemocytes, and provide additional molecular evidence that reinforces the hypothesis that these hemocytes may function as neural precursors in adult neurogenesis.

The online version contains supplementary material available at 10.1007/s10571-026-01686-x.

## Linked entities

- **Genes:** 5-HT7 (5-hydroxytryptamine (serotonin) receptor 7) [NCBI Gene 43669]
- **Chemicals:** serotonin (PubChem CID 5202)

## Full-text entities

- **Genes:** brat (brain tumor) [NCBI Gene 35197] {aka CG10719, Cf, Dmel\CG10719, E60, anon-37CDa, fs(2)ltoPM43}, PCNA (Proliferating cell nuclear antigen) [NCBI Gene 37290] {aka 53/13, CG9193, DmPCNA, DmPCNA1, Dmel\CG9193, MUS209}, NUMB (NUMB endocytic adaptor protein) [NCBI Gene 8650] {aka C14orf41, S171, c14_5527}, PCNA (proliferating cell nuclear antigen) [NCBI Gene 5111] {aka ATLD2}, Poxn (Pox neuro) [NCBI Gene 36741] {aka CG8246, Dmel\CG8246, P4, Pox-n, Poxn1, neuro}, N (Notch) [NCBI Gene 31293] {aka 1.1, 16-178, 16-55, Ax, CG3936, CT13012}, SoxN (SoxNeuro) [NCBI Gene 44275] {aka CG18024, DM64, Dmel\CG18024, SOX29F, SOXB1, Sox B1}, ast (asteroid) [NCBI Gene 33282] {aka CG4426, Dmel\CG4426, S[r], Star/asteroid}, pros (prospero) [NCBI Gene 41363] {aka 0244/09, 0320/10, 0441/16, 0451/09, 0563/18, 0585/13}, Hml (Hemolectin) [NCBI Gene 39529] {aka CG7002, CT21553, Dmel\CG7002, d-hml}, QSOX2 (quiescin sulfhydryl oxidase 2) [NCBI Gene 169714] {aka QSCN6L1, SOXN}, 5-HT7 (5-hydroxytryptamine (serotonin) receptor 7) [NCBI Gene 43669] {aka 5-HT-7, 5-HT-dro, 5-HT-dro1, 5-HT2A, 5-HT7Dro, 5-HT[7]Dro}, DCX-EMAP (Doublecortin-domain-containing echinoderm-microtubule-associated protein) [NCBI Gene 39617] {aka CG13466, CG13467, CG42247, Dmel\CG42247, Dmel_CG13466, Dmel_CG13467}, DCX (doublecortin) [NCBI Gene 1641] {aka DBCN, DC, LISX, SCLH, XLIS}, numb (numb) [NCBI Gene 34263] {aka CG3779, Dmel\CG3779, N7-1, Nb, d-numb, dNumb}, gcm (glial cells missing) [NCBI Gene 34277] {aka CG12245, Dmel\CG12245, GCM1, GCMa, N7-4, glide}, AstA (Allatostatin A) [NCBI Gene 42947] {aka ALLS, AS, ASA, AST, AST-1, AST-3}, 5-HT1A (5-hydroxytryptamine (serotonin) receptor 1A) [NCBI Gene 37196] {aka 5-HT, 5-HT-1a, 5-HT-dro2A, 5-HT1ADro, 5-HT[1A]Dro, 5-HT[[1ADro]]}
- **Diseases:** tissue (MESH:D017695), loss of mobility (MESH:D014086), brain damage (MESH:D001925), brain (MESH:D001927), Acute Brain Injury (MESH:D001930), HPT (MESH:D019337), bleeding (MESH:D006470), weakness (MESH:D018908), HS (MESH:C567159), traumatic brain injury (MESH:D000070642), neurodegeneration (MESH:D019636), injury (MESH:D014947)
- **Chemicals:** eosin (MESH:D004801), KCl (MESH:D011189), DAPI (MESH:C007293), 5-HT (MESH:D012701), Formaldehyde (MESH:D005557), paraformaldehyde (MESH:C003043), LPS (MESH:D008070), Hoechst 33342 (MESH:C017807), H&amp;E (MESH:D006371), NaHCO3 (MESH:D017693), MgCl2.6H2O (-), hematoxylin (MESH:D006416), CaCl2 (MESH:D002122), EdU (MESH:C022811), ethanol (MESH:D000431), Hoechst 33258 (MESH:D006690), water (MESH:D014867), xylene (MESH:D014992), NaCl (MESH:D012965), paraffin (MESH:D010232), phosphate (MESH:D010710), DEPC (MESH:D004047)
- **Species:** Drosophila melanogaster (fruit fly, species) [taxon 7227], Bos taurus (bovine, species) [taxon 9913], Procambarus clarkii (red swamp crayfish, species) [taxon 6728], Homo sapiens (human, species) [taxon 9606], Astacoidea (crayfish, superfamily) [taxon 6724], Ucides cordatus (species) [taxon 184468], Macrobrachium rosenbergii (giant freshwater prawn, species) [taxon 79674], Panulirus argus (Caribbean spiny lobster, species) [taxon 6737], Pacifastacus leniusculus (signal crayfish, species) [taxon 6720]
- **Cell lines:** 3Ci — Homo sapiens (Human), B-cell non-Hodgkin lymphoma, Cancer cell line (CVCL_1861)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12936283/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12936283/full.md

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Source: https://tomesphere.com/paper/PMC12936283