# Paradoxes in the Ontological Classification of Glia—Evidence for an Important New Class of Brain Cells with Primary Functions in Iron Regulation

**Authors:** Adrienne E. Milward, Rebecca J. Hood, Chan-An Lin, Conceição Bettencourt, Elvis Acquah, Jake Brooks, Joanna F. Collingwood, Yoshiteru Kagawa, Samantha J. Richardson, Yuting Wu, Yi Lu, Mirella Dottori, Daniel M. Johnstone

PMC · DOI: 10.3390/cells15060511 · 2026-03-13

## TL;DR

This paper proposes a new class of brain cells called 'ferriglia' that primarily regulate iron, challenging existing classifications of glial cells.

## Contribution

The paper introduces 'ferriglia' as a novel class of glial cells with primary functions in iron regulation.

## Key findings

- Current glial paradigms show discrepancies in empirical, evolutionary, and pragmatic perspectives.
- A subset of iron-rich glial cells may have primary functions in iron regulation rather than myelination.
- Ferriglia may play a role in various neurological and psychiatric disorders.

## Abstract

The ontological categorization of the cellular elements of the brain was proposed over a century ago by Santiago Ramón y Cajal (neurons, astroglia) and Pío del Río-Hortega (oligodendroglia, microglia). It combines histochemical observations of morphology with allied inferences about the specialized functions and origins (ectoderm or mesoderm) of each cellular element. This ontology shapes modern neuroscience, with the main non-neuronal cells—astroglia, oligodendroglia and microglia—viewed as having distinct primary roles relating respectively to the metabolic support, myelination and immunoprotection of neurons, the information signaling cells. Yet contemporary techniques, ranging from electrophysiology to single-cell transcriptomics and ultrahigh resolution spectroscopy, are revealing intersecting molecular profiles and functional capacities of these cell groups, for example metabolic support, neuroimmune and signaling functions in oligodendroglia. Here we identify discrepancies in current glial paradigms, from empirical, evolutionary and pragmatic perspectives. We suggest a subset of small, iron-rich glial cells, usually with few processes, often viewed as oligodendroglia with myelin-related primary functions, instead have iron-related primary functions that are central to all aspects of brain activity. We call these ‘ferriglia’. We discuss implications for pathogenesis across the spectrum of neuropsychiatric and neurological disorders, including neurodegenerative conditions such as Alzheimer’s disease and other less common cognitive, movement and neurobehavioral disorders, stroke and cerebrovascular disease, glioblastoma and other brain cancers and neuroimmune conditions. We also briefly address the question of where ferriglia may reside within existing glial compartments and lineages, implications for the ontological classification of other glial cells, and research challenges that must be overcome going forward.

## Linked entities

- **Chemicals:** iron (PubChem CID 23925)
- **Diseases:** Alzheimer’s disease (MONDO:0004975), glioblastoma (MONDO:0018177), stroke (MONDO:0005098), cerebrovascular disease (MONDO:0011057)

## Full-text entities

- **Genes:** AIF1 (allograft inflammatory factor 1) [NCBI Gene 199] {aka AIF-1, IBA1, IRT-1, IRT1}, SLC40A1 (solute carrier family 40 member 1) [NCBI Gene 30061] {aka FPN, FPN1, HFE4, IREG1, MST079, MSTP079}, MOBP (myelin associated oligodendrocyte basic protein) [NCBI Gene 4336], NEUROD1 (neuronal differentiation 1) [NCBI Gene 4760] {aka BETA2, BHF-1, MODY6, NEUROD, T2D, bHLHa3}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CCL14 (C-C motif chemokine ligand 14) [NCBI Gene 6358] {aka CC-1, CC-3, CKB1, HCC-1, HCC-1(1-74), HCC-1/HCC-3}, MELTF (melanotransferrin) [NCBI Gene 4241] {aka CD228, MAP97, MFI2, MTF1, MTf}, Olig2 (oligodendrocyte transcription factor 2) [NCBI Gene 50913] {aka Bhlhb1, Olg-2, Oligo2, RK17, bHLHe19}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, HFE (homeostatic iron regulator) [NCBI Gene 3077] {aka HFE1, HH, HLA-H, MVCD7, TFQTL2}, FXN (frataxin) [NCBI Gene 2395] {aka CyaY, FA, FARR, FRDA, X25}, TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}, CSPG4 (chondroitin sulfate proteoglycan 4) [NCBI Gene 1464] {aka CSPG4A, HMW-MAA, MCSP, MCSPG, MEL-CSPG, MSK16}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, Plp1 (proteolipid protein (myelin) 1) [NCBI Gene 18823] {aka DM20, Plp, jimpy, jp, msd, rsh}, Mbp (myelin basic protein) [NCBI Gene 17196] {aka Hmbpr, golli-mbp, jve, mld, shi}, PDGFRB (platelet derived growth factor receptor beta) [NCBI Gene 5159] {aka CD140B, IBGC4, IMF1, JTK12, KOGS, OPDKD}, NEO1 (neogenin 1) [NCBI Gene 4756] {aka IGDCC2, NGN, NTN1R2}, PHB2 (prohibitin 2) [NCBI Gene 11331] {aka BAP, BCAP37, Bap37, PNAS-141, REA, hBAP}, PDGFRA (platelet derived growth factor receptor alpha) [NCBI Gene 5156] {aka CD140A, PDGFR-2, PDGFR2}, GLUL (glutamate-ammonia ligase) [NCBI Gene 2752] {aka DEE116, GLNS, GS, PIG43, PIG59}, WNT2 (Wnt family member 2) [NCBI Gene 7472] {aka INT1L1, IRP}, NRF1 (nuclear respiratory factor 1) [NCBI Gene 4899] {aka ALPHA-PAL}, NKX2-2 (NK2 homeobox 2) [NCBI Gene 4821] {aka NKX2.2, NKX2B}, ACO1 (aconitase 1) [NCBI Gene 48] {aka ACONS, HEL60, IREB1, IREBP, IREBP1, IRP1}, Tsf1 (Transferrin 1) [NCBI Gene 32821] {aka 143958_at, CG6186, Dmel\CG6186, Tf, Trf, anon-EST:Posey265}, GTF2E1 (general transcription factor IIE subunit 1) [NCBI Gene 2960] {aka FE, TF2E1, TFIIE-A}, RTN4 (reticulon 4) [NCBI Gene 57142] {aka ASY, NI220/250, NOGO, NOGOA, NOGOB, NSP}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, Cnp (2',3'-cyclic nucleotide 3' phosphodiesterase) [NCBI Gene 12799] {aka CNPase, Cnp-1, Cnp1}, SLC11A1 (solute carrier family 11 member 1) [NCBI Gene 6556] {aka LSH, NRAMP, NRAMP1}, SLC11A2 (solute carrier family 11 member 2) [NCBI Gene 4891] {aka AHMIO1, DCT1, DMT1, NRAMP2}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, SOX10 (SRY-box transcription factor 10) [NCBI Gene 6663] {aka DOM, PCWH, SOX-10, WS2E, WS4, WS4C}, CNP (2',3'-cyclic nucleotide 3' phosphodiesterase) [NCBI Gene 1267] {aka CN37, CNP1, HLD20}, FECH (ferrochelatase) [NCBI Gene 2235] {aka EPP, EPP1, FCE}, OLIG2 (oligodendrocyte transcription factor 2) [NCBI Gene 10215] {aka BHLHB1, OLIGO2, PRKCBP2, RACK17, bHLHe19}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, FTH1 (ferritin heavy chain 1) [NCBI Gene 2495] {aka FHC, FTH, FTHL6, HFE5, NBIA9, PIG15}
- **Diseases:** alpha synucleinopathies (MESH:D000080874), neuronal atrophy (MESH:D001284), dystonia (MESH:D004421), iron overload (MESH:D019190), infarct (MESH:D007238), Amyloidosis (MESH:D000686), myelin disorders (MESH:D003711), synaptic degeneration (MESH:D012183), Stroke (MESH:D020521), neurosensory or motor impairment (MESH:D006319), FRDA (MESH:D005621), infection (MESH:D007239), cerebrovascular hemorrhage (MESH:D006470), injury to (MESH:D014947), ischemic stroke (MESH:D002544), Nervous System (MESH:D009422), CNS Infections (MESH:D002494), degenerative disease (MESH:D019636), toxicity (MESH:D064420), iron insufficiency (MESH:D000309), neuropsychiatric conditions (MESH:D001523), multiple system atrophy (MESH:D019578), cognitive impairment (MESH:D003072), PD (MESH:D010300), Brain Diseases (MESH:D001927), glioblastoma (MESH:D005909), motor disability (MESH:D009069), cancer (MESH:D009369), progressive supranuclear palsy (MESH:D013494), gliosis (MESH:D005911), parkinsonism (MESH:D010302), MSA (MESH:C537381), Cerebrovascular Disease (MESH:D002561), ataxia (MESH:D001259), ischemic (MESH:D002545), Neuroimmune Disorders (MESH:D009358), dementia (MESH:D003704), chorea (MESH:D002819), neuroimmune conditions (MESH:D020763), Siderosis (MESH:D012806), Gliomas (MESH:D005910), ischemic damage (MESH:D017202), iron (MESH:D000090463), cerebellar and sensory ataxia (MESH:D002524), NBIA (MESH:D006211), speech and swallowing deficits (MESH:D003680), inflammatory (MESH:D007249), genetic disease (MESH:D030342), cerebrovascular amyloid angiopathy (MESH:C538248), Brain Cancers (MESH:D001932), neurological disorders (MESH:D009461), Hereditary Neuroferritinopathy (MESH:D009386), Amyloid (MESH:C000718787), AD (MESH:D000544), impairment of the autonomic nervous system (MESH:D001342)
- **Chemicals:** oxygen (MESH:D010100), chitin (MESH:D002686), 3,3'-diaminobenzidine (MESH:D015100), citrate (MESH:D019343), hydrogen (MESH:D006859), GABA (MESH:D005680), sulfate (MESH:D013431), Fe2+ (-), K+ (MESH:D011188), Berlin blue (MESH:C000170), fat (MESH:D005223), Lipid (MESH:D008055), Fe (MESH:D007501), eosin (MESH:D004801), DAB (MESH:C000469), glutamate (MESH:D018698), phospholipid (MESH:D010743), glycogen (MESH:D006003), amino acids (MESH:D000596), formalin (MESH:D005557), iron carbides (MESH:C541825), dopamine (MESH:D004298), water (MESH:D014867), hydrocarbons (MESH:D006838), heme (MESH:D006418), Melanin (MESH:D008543), hemotoxylin (MESH:D006416), ATP (MESH:D000255), metal (MESH:D008670)
- **Species:** Myxine glutinosa (Atlantic hagfish, species) [taxon 7769], Cercopithecidae (monkey, family) [taxon 9527], Ctenophora (genus) [taxon 1003038], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Selachii (sharks, infraclass) [taxon 119203], Sepiidae (cuttlefishes, family) [taxon 6608], Hydra (genus) [taxon 6083], Mus musculus (house mouse, species) [taxon 10090], Drosophila melanogaster (fruit fly, species) [taxon 7227], Holothuroidea (holothurians, class) [taxon 7705], Deuterostomia (deuterostomes, clade) [taxon 33511], Ovis aries (domestic sheep, species) [taxon 9940], Porifera (sponges, phylum) [taxon 6040], Placozoa (placozoan, phylum) [taxon 10226], Actiniaria (actinians, order) [taxon 6103], Homo sapiens (human, species) [taxon 9606], Tripedalia (genus) [taxon 6140], Ascidiacea (sea squirts, class) [taxon 7713], Anthozoa (anthozoans, class) [taxon 6101], Rattus norvegicus (brown rat, species) [taxon 10116], Petromyzontidae (lampreys, family) [taxon 7746], Octopus (genus) [taxon 6643], Echinodermata (echinoderms, phylum) [taxon 7586], Protostomia (clade) [taxon 33317], Astacoidea (crayfish, superfamily) [taxon 6724], Nematostella vectensis (starlet sea anemone, species) [taxon 45351], Branchiostomatidae (amphioxi, family) [taxon 7736]
- **Mutations:** Tyr69His
- **Cell lines:** HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13025143/full.md

---
Source: https://tomesphere.com/paper/PMC13025143