# Folate Receptor Alpha (FRα) and the Developing Brain: From Molecular Function to Neurodevelopmental Outcomes

**Authors:** Olga Egorova, Erik Domellöf, Maryam Ardalan, Carina Mallard

PMC · DOI: 10.1007/s12035-026-05813-z · Molecular Neurobiology · 2026-03-25

## TL;DR

This review explores how the Folate Receptor Alpha (FRα) influences brain development and function, linking folate metabolism to neurological outcomes.

## Contribution

The paper synthesizes current knowledge on FRα's roles in brain development and its implications for neurodevelopmental and neuropsychiatric conditions.

## Key findings

- FRα is essential for transporting folate into the CNS and regulating cellular processes.
- Impaired FRα function is linked to developmental abnormalities and neurological dysfunction.
- FRα autoantibodies and folate supplementation show potential for diagnosis and treatment.

## Abstract

Folate receptor alpha (FRα) is a high-affinity transporter responsible for delivering folate (vitamin B9) into the central nervous system (CNS), supporting the synthesis of nucleic acids, amino acids, lipids, and signaling molecules through one-carbon transfer pathways. Beyond its transport function, upon activation by folate, FRα modulates extracellular signaling, regulates membrane and cytosolic proteins, and gene transcription. Disruption of FRα, whether functional or structural, can impair CNS folate availability and lead to developmental abnormalities or neurological dysfunction, with the clinical consequences depending on the timing, severity, and presumably on the individual genetic background. Together, these insights position FRα as both a multifunctional regulator of cellular fate and a key molecular interface connecting folate metabolism, brain development, and neurobehavioral outcomes. This narrative review synthesizes the current state of knowledge on FRα, highlighting its roles in neuronal and glial differentiation, CNS maturation, and neural plasticity, while also examining the links between impaired FRα function and a spectrum of developmental and neuropsychiatric conditions. It also outlines the need for broader population-based studies to evaluate the diagnostic value of FRα autoantibodies and the therapeutic potential of folate supplementation.

## Linked entities

- **Proteins:** FOSL1 (FOS like 1, AP-1 transcription factor subunit)
- **Chemicals:** folate (PubChem CID 135405876), vitamin B9 (PubChem CID 135398658)

## Full-text entities

- **Genes:** LYN (LYN proto-oncogene, Src family tyrosine kinase) [NCBI Gene 4067] {aka JTK8, SAIDV, p53Lyn, p56Lyn}, MTHFR (methylenetetrahydrofolate reductase) [NCBI Gene 4524], FOLR1 (folate receptor alpha) [NCBI Gene 2348] {aka FBP, FOLR, FR-alpha, FRalpha, NCFTD}, FOLR3 (folate receptor gamma) [NCBI Gene 2352] {aka FR-G, FR-gamma, FRgamma, gamma-hFR}, Rabep2 (rabaptin, RAB GTPase binding effector protein 2) [NCBI Gene 70314] {aka 2610011A08Rik, Fra}, Shroom3 (shroom family member 3) [NCBI Gene 27428] {aka D5Ertd287e, Shrm, Shrm3}, GADD45A (growth arrest and DNA damage inducible alpha) [NCBI Gene 1647] {aka DDIT1, GADD45}, SLC46A1 (solute carrier family 46 member 1) [NCBI Gene 113235] {aka G21, HCP1, HsPCFT, PCFT, hPCFT}, Rho (rhodopsin) [NCBI Gene 212541] {aka Noerg1, Opn2, Ops, RP4}, SLC19A1 (solute carrier family 19 member 1) [NCBI Gene 6573] {aka CHMD, FOLT, IFC-1, IFC1, IMD114, MEGAF}, IZUMO1R (IZUMO1 receptor, JUNO) [NCBI Gene 390243] {aka FOLR4, FR-delta, Folbp3, JUNO}, FOSL1 (FOS like 1, AP-1 transcription factor subunit) [NCBI Gene 8061] {aka FRA, FRA1, fra-1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PAX3 (paired box 3) [NCBI Gene 5077] {aka CDHS, HUP2, PAX-3, WS1, WS3}, Pax3 (paired box 3) [NCBI Gene 18505] {aka Pax-3, Sp, Splchl2, splotch}, Src (src proto-oncogene, non-receptor tyrosine kinase) [NCBI Gene 20779] {aka pp60c-src}, FOLR2 (folate receptor beta) [NCBI Gene 2350] {aka BETA-HFR, FBP, FBP/PL-1, FR-BETA, FR-P3, FRbeta}, KITLG (KIT ligand) [NCBI Gene 4254] {aka DCUA, DFNA69, FPH2, FPHH, KL-1, Kitl}, FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, Matk (megakaryocyte-associated tyrosine kinase) [NCBI Gene 17179] {aka CHK, HYL, Ntk, p56ntk}
- **Diseases:** depression (MESH:D003866), ischemic brain injury (MESH:D001930), neurodevelopmental disorders (MESH:D002658), folate (MESH:C562799), schizophrenia (MESH:D012559), cognitive or behavioral dysfunction (MESH:D003072), neurodevelopmental and neuropsychiatric conditions (MESH:D001523), cancer (MESH:D009369), neural tube defects (MESH:D009436), brain disorders (MESH:D001927), ASD (MESH:D000067877), neurometabolic disorder (MESH:D009358), inflammation (MESH:D007249), developmental abnormalities (MESH:D006130), neuronal damage (MESH:D009410), embryonic lethality (MESH:D020964), neurological dysfunction (MESH:D009461), CFD (MESH:C567791)
- **Chemicals:** carbon (MESH:D002244), cholesterol (MESH:D002784), Ca2+ (-), GPI (MESH:D017261), calcium (MESH:D002118), 5-MTHF (MESH:C005984), lipid (MESH:D008055), N-methyl-D-aspartate (MESH:D016202), folinic acid (MESH:D002955), sphingomyelin (MESH:D013109), polyglutamate (MESH:D011099), amino acids (MESH:D000596), pteridine (MESH:D011621), glutamate (MESH:D018698), Folate (MESH:D005492), organic phosphate (MESH:D010755), lysine (MESH:D008239), nucleotide (MESH:D009711), Dopaminergic (MESH:D004298), p-aminobenzoic acid (MESH:D010129)
- **Species:** Danio rerio (leopard danio, species) [taxon 7955], Mus musculus (house mouse, species) [taxon 10090], Bos taurus (bovine, species) [taxon 9913], Homo sapiens (human, species) [taxon 9606], C. elegans [taxon 328850], Xenopus laevis (African clawed frog, species) [taxon 8355], Gallus gallus (bantam, species) [taxon 9031]
- **Mutations:** 1561C>T, 677C>T

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13018024/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC13018024/full.md

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Source: https://tomesphere.com/paper/PMC13018024