# Slc6a9 is distributed in glial cells and neurons across several nervous system regions, whereas Slc6a5 is more restricted to neurons in the caudal brain

**Authors:** Mikaela M. Ceder, Malin C. Lagerström

PMC · DOI: 10.1186/s12868-026-00999-3 · BMC Neuroscience · 2026-02-17

## TL;DR

This study maps the distribution of two glycine transporter genes in mouse brains and peripheral organs, revealing differences in cell types and sex-related expression patterns.

## Contribution

The study provides new insights into the spatial and sex-dependent expression patterns of Slc6a9 and Slc6a5 in the mouse nervous system.

## Key findings

- Slc6a9 is broadly expressed in glial cells and neurons across multiple brain regions.
- Slc6a5 is more restricted to neurons in the caudal brain.
- Sex-dependent differences in expression were observed for both genes in various brain regions and organs.

## Abstract

The glycinergic system constitutes a main source of inhibitory regulation in the central nervous system. Glycine transporters (GLYT1 and GLYT2), encoded by Slc6a9 and Slc6a5, respectively, are responsible for glycine reuptake and clearance from the synaptic cleft, thereby maintaining neurotransmitter homeostasis. Emerging evidence from pharmacological and mechanistic studies has highlighted GLYTs as promising therapeutic targets for psychiatric disorders and persistent pain. Nevertheless, data on anatomical and cellular distribution of GLYTs and sex-dependent differences in GLYT expression remain limited.

To address this gap, the aim of this study was to examine the Slc6a9 and Slc6a5 mRNA expression across mouse brain regions and peripheral organs using three complementary approaches focusing on mRNA expression: re-analysis of single-cell RNA sequencing data, quantitative RT-PCR, and RNAscope.

Both genes were detected in multiple brain regions, with Slc6a9 exhibiting a broader distribution in both glial cells and neurons, while Slc6a5 was more restricted to neurons. Sex-dependent differences were detected for Slc6a9 in the amygdala and thalamus, liver, intestine, spleen, kidney and genitalia using quantitative RT-PCR, and for Slc6a5 in the cortex, striatum, hippocampus, and spinal cord using quantitative RT-PCR. Spatial analysis of the glycine transporters showed that Slc6a9 can be found in several brain regions spanning the rostral to the caudal axis, in both glial cells and neurons, while Slc6a5 was more restricted to the caudal brain regions.

In general, in regions where differences were detected using quantitative RT-PCR, higher expression levels were observed in male mice. Moreover, Slc6a9 expression was found to occur in both glial cells, such as astrocytes, oligodendrocytes and ependymal cells, as well as both excitatory and inhibitory neurons, while Slc6a5 mainly occurred in inhibitory neurons. These findings provide novel insights into the spatial and sex-dependent expression of glycine transporters.

The online version contains supplementary material available at 10.1186/s12868-026-00999-3.

## Linked entities

- **Genes:** SLC6A9 (solute carrier family 6 member 9) [NCBI Gene 6536], SLC6A5 (solute carrier family 6 member 5) [NCBI Gene 9152]
- **Proteins:** MGAT1 (alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase), GGTA1 (glycoprotein alpha-galactosyltransferase 1 (inactive))
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Ppia (peptidylprolyl isomerase A) [NCBI Gene 268373] {aka Cphn, CyP-18, CypA, SP18}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, Slc32a1 (solute carrier family 32 (GABA vesicular transporter), member 1) [NCBI Gene 22348] {aka VGAT, Viaat}, Glra3 (glycine receptor, alpha 3 subunit) [NCBI Gene 110304], Mbp (myelin basic protein) [NCBI Gene 17196] {aka Hmbpr, golli-mbp, jve, mld, shi}, SLC6A5 (solute carrier family 6 member 5) [NCBI Gene 9152] {aka GLYT-2, GLYT2, HKPX3, NET1}, Car4 (carbonic anhydrase 4) [NCBI Gene 12351] {aka Ca4}, Actr1b (ARP1 actin-related protein 1B, centractin beta) [NCBI Gene 226977] {aka 2310066K23Rik, Arp1b}, Wnt1 (wingless-type MMTV integration site family, member 1) [NCBI Gene 22408] {aka Int-1, Wnt-1, sw, swaying}, Slc17a6 (solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6) [NCBI Gene 140919] {aka 2900073D12Rik, DNPI, VGLUT2}, Gpr158 (G protein-coupled receptor 158) [NCBI Gene 241263] {aka 5330427M13Rik, mGlyR, mKIAA1136}, Rbfox3 (RNA binding protein, fox-1 homolog (C. elegans) 3) [NCBI Gene 52897] {aka Fox-3, Hrnbp3, NeuN, Neuna60}, Sdtq11 (skull development traits QTL 11) [NCBI Gene 100035930] {aka L19}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Slc6a5 (solute carrier family 6 (neurotransmitter transporter, glycine), member 5) [NCBI Gene 104245] {aka Glyt2, prestin}, Rpl19 (ribosomal protein L19) [NCBI Gene 19921], SLC6A9 (solute carrier family 6 member 9) [NCBI Gene 6536] {aka GCENSG, GLYT1, IS6}, Foxj1 (forkhead box J1) [NCBI Gene 15223] {aka FKHL-13, HFH-4, Hfh4}, Slc6a9 (solute carrier family 6 (neurotransmitter transporter, glycine), member 9) [NCBI Gene 14664] {aka Glyt-1, Glyt1}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580]
- **Diseases:** respiratory failure (MESH:D012131), essential hypertension (MESH:D000075222), major depressive disorder (MESH:D003865), adolescent idiopathic scoliosis (OMIM:181800), pain (MESH:D010146), schizophrenia (MESH:D012559), psychiatric disorders (MESH:D001523), chronic pain (MESH:D059350), dislocation (MESH:D004204), hyperekplexia (MESH:D000071017), mechanical allodynia (MESH:D006930), encephalopathy (MESH:D001927), MCL (MESH:C535516), hypotonia (MESH:D009123), startle (MESH:D016750)
- **Chemicals:** iron (MESH:D007501), water (MESH:D014867), Glycine (MESH:D005998), chloride (MESH:D002712), N-methyl-D-aspartate (MESH:D016202), glutamate (MESH:D018698), acid (MESH:D000143), Triton X-100 (MESH:D017830), FITC (MESH:D016650), Ketalar (MESH:D007649), formaldehyde (MESH:D005557), 4',6-diamidino-2-phenylindole (MESH:C007293), Cy5 (MESH:C085321), PBS (MESH:D007854), Tween-20 (MESH:D011136), sodium (MESH:D012964), Domitor (-), Medetomidine (MESH:D020926), isopentane (MESH:C067038), amino acid (MESH:D000596)
- **Species:** Pan troglodytes (chimpanzee, species) [taxon 9598], Sus scrofa (pig, species) [taxon 9823], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Mutations:** C in 0, rs4354668, rs2486001, rs2000959
- **Cell lines:** -1 — Mus musculus (Mouse), Hybridoma (CVCL_C7RB), /6J — Homo sapiens (Human), Cutaneous melanoma, Cancer cell line (CVCL_W797), C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12931055/full.md

## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12931055/full.md

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Source: https://tomesphere.com/paper/PMC12931055