# Spectrum and functions of ion channels and transporters in osteoclasts

**Authors:** Hongyu Chen, Yanli Zhang, Yulong Zhu, Xiang Xiao, Shanshan Huang, Xiaohong Duan

PMC · DOI: 10.1038/s41413-026-00513-9 · 2026-03-27

## TL;DR

This paper reviews ion channels and transporters in osteoclasts, highlighting their roles in bone function and disease, and potential for new therapies.

## Contribution

The paper systematically categorizes nearly 90 osteoclastic ion channels and transporters and discusses their roles in disease and potential therapeutic applications.

## Key findings

- Hydrogen, chloride, phosphate, and calcium transporters are critical for osteoclast function.
- Advanced techniques reveal more channels and transporters in osteoclasts than previously understood.
- Targeting these ion channels could lead to new therapies for bone disorders.

## Abstract

Osteoclasts are essential for bone resorption and interact with osteoblasts during bone remodeling. Ion channels and transporters located in the ruffled border or intracellular vesicles coordinate the transport of various ions and substrates, which is fundamental to the primary functions of osteoclasts. Numerous channels and transporters are implicated in bone metabolic disorders and genetic diseases. Among these, the voltage-gated chloride channel 7 (ClC-7) and vacuolar proton ATPases (V-ATPase) represent the most well-characterized examples in osteoclasts. Using the classification system of the Transporter Classification Database, we reviewed nearly 90 osteoclastic ion channels and transporters, categorizing them into six groups: ATPases, cation channels, anion channels, complex transporters, organic substance transporters, and ATP-binding cassette transporters. We summarized recent advances in their subcellular localization, transported substrates, associated diseases, and physiological roles in relevant biological functions and signaling pathways. Notably, transporters for hydrogen, chloride, phosphate, and calcium are particularly critical for osteoclast function. We also reviewed therapeutic candidates targeting these ion channels and discussed strategies for their future development. As transcriptome and other advanced techniques have identified more channels and transporters in osteoclasts, the diversity and unexplored functions of these molecules may exceed previous understanding. Increased attention to their widespread distributions and interactions could reveal new therapeutic targets for osteoclast-related and other bone disorders.

## Linked entities

- **Proteins:** CLCN7 (Cl-/H+ antiporter 7), VhaSFD (Vacuolar H[+]-ATPase SFD subunit)

## Full-text entities

- **Genes:** ATP6AP1 (ATPase H+ transporting accessory protein 1) [NCBI Gene 537] {aka 16A, ATP6IP1, ATP6S1, Ac45, CF2, VATPS1}, Trpv4 (transient receptor potential cation channel, subfamily V, member 4) [NCBI Gene 63873] {aka 0610033B08Rik, OTRPC4, Trp12, VR-OAC, VRL-2, VROAC}, Clcn1 (chloride channel, voltage-sensitive 1) [NCBI Gene 12723] {aka Clc-1, Clc1, SMCC1, adr, mto, myotonia}, Trpv2 (transient receptor potential cation channel, subfamily V, member 2) [NCBI Gene 22368] {aka GRC, OTRPC2, VRL-1, Vrl1}, Ppp2ca (protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform) [NCBI Gene 19052] {aka PP2A}, Pink1 (PTEN induced putative kinase 1) [NCBI Gene 68943] {aka 1190006F07Rik, BRPK, mFLJ00387}, Slc25a19 (solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19) [NCBI Gene 67283] {aka 2900089E13Rik, DNC, MUP1, TPC}, Tcirg1 (T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3) [NCBI Gene 27060] {aka ATP6N1C, ATP6a3, Atp6i, OC-116, OPTB1, Stv1}, Slc5a2 (solute carrier family 5 (sodium/glucose cotransporter), member 2) [NCBI Gene 246787] {aka Sglt2}, Slc1a3 (solute carrier family 1 (glial high affinity glutamate transporter), member 3) [NCBI Gene 20512] {aka B430115D02Rik, Eaat1, GLAST, GLAST-1, GLU-T, GluT-1}, Cacna1d (calcium channel, voltage-dependent, L type, alpha 1D subunit) [NCBI Gene 12289] {aka 8430418G19Rik, Cach3, Cacn4, Cacnl1a2, Cav1.3, Cchl1a}, Src (src proto-oncogene, non-receptor tyrosine kinase) [NCBI Gene 20779] {aka pp60c-src}, Trpv6 (transient receptor potential cation channel, subfamily V, member 6) [NCBI Gene 64177] {aka CAT, CaT1, Cac, Ecac2, Otrpc3}, Nfatc1 (nuclear factor of activated T-cells 1) [NCBI Gene 100361818], Clca3a1 (chloride channel accessory 3A1) [NCBI Gene 12722] {aka Cacc, Clca1}, Ano5 (anoctamin 5) [NCBI Gene 233246] {aka 9330162L24, Gdd1, Tmem16e}, Tfrc (transferrin receptor) [NCBI Gene 22042] {aka 2610028K12Rik, CD71, E430033M20Rik, Mtvr1, TFR, TFR1}, Ryr1 (ryanodine receptor 1, skeletal muscle) [NCBI Gene 20190] {aka RYR-1, Ryr, skrr}, Slc1a7 (solute carrier family 1 (glutamate transporter), member 7) [NCBI Gene 242607] {aka A930031E15Rik, Eaat5}, Sigmar1 (sigma non-opioid intracellular receptor 1) [NCBI Gene 18391] {aka Oprs1, Sig1R, sigma1R}, Ptk2b (protein tyrosine kinase 2 beta) [NCBI Gene 50646] {aka CAK beta, CAKB, CAKbeta, Pyk2}, P2rx7 (purinergic receptor P2X, ligand-gated ion channel, 7) [NCBI Gene 18439] {aka P2X(7), P2X7R}, Slc23a2 (solute carrier family 23 (nucleobase transporters), member 2) [NCBI Gene 54338] {aka NBTL1, SVCT2, Slc23a1, YSPL2, YSPL3, mKIAA0238}, Tcf3 (transcription factor 3) [NCBI Gene 21423] {aka A1, ALF2, E12, E12/E47, E2A, E47}, Ibsp (integrin-binding sialoprotein) [NCBI Gene 24477] {aka Bsp}, Slc9a6 (solute carrier family 9 (sodium/hydrogen exchanger), member 6) [NCBI Gene 236794] {aka 3732426M05, 6430520C02Rik, NHE-6, NHE6, mKIAA0267}, Slc12a4 (solute carrier family 12, member 4) [NCBI Gene 20498] {aka KCC1, RBCKCC1}, Fos (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 14281] {aka D12Rfj1, c-fos, cFos}, Fxyd5 (FXYD domain-containing ion transport regulator 5) [NCBI Gene 60338] {aka RIC}, CLIC4 (CLIC family member 4) [NCBI Gene 25932] {aka CLIC4L, H1, MTCLIC, huH1, p64H1}, CLC [NCBI Gene 12735], Itpr3 (inositol 1,4,5-triphosphate receptor 3) [NCBI Gene 16440] {aka IP3R 3, IP3R-3, Ip3r3, Itpr-3, tf}, Nherf2 (NHERF family PDZ scaffold protein 2) [NCBI Gene 65962] {aka 0610011L07Rik, 1200011K07Rik, 2010007A20Rik, E3karp, NHERF-2, Octs2}, Hcn1 (hyperpolarization activated cyclic nucleotide gated potassium channel 1) [NCBI Gene 15165] {aka Bcng1, C630013B14Rik, HAC2}, Slc9a1 (solute carrier family 9 (sodium/hydrogen exchanger), member 1) [NCBI Gene 20544] {aka Apnh, Mir5122, Nhe1, mir-5122, swe}, Atp2b4 (ATPase, Ca++ transporting, plasma membrane 4) [NCBI Gene 381290] {aka Pmca4}, SLC1A5 (solute carrier family 1 member 5) [NCBI Gene 6510] {aka AAAT, ASCT2, ATBO, M7V1, M7VS1, R16}, Slc11a2 (solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2) [NCBI Gene 18174] {aka DCT1, DMT1, Nramp2, mk, van}, Slc4a8 (solute carrier family 4 (anion exchanger), member 8) [NCBI Gene 59033] {aka C230026C11, NDCBE, kNBC-3}, Tfeb (transcription factor EB) [NCBI Gene 21425] {aka Tcfeb, bHLHe35}, Zbtb8os (zinc finger and BTB domain containing 8 opposite strand) [NCBI Gene 67106] {aka 2010001H09Rik, 2310028N13Rik, Arch, Archm}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, Kcnma1 (potassium large conductance calcium-activated channel, subfamily M, alpha member 1) [NCBI Gene 16531] {aka 5730414M22Rik, BKCA alpha, BKCa, KCa1.1, MaxiK, Slo}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, Kcna3 (potassium voltage-gated channel, shaker-related subfamily, member 3) [NCBI Gene 16491] {aka Kca1-3, Kv1.3, Mk-3}, Abcb4 (ATP-binding cassette, sub-family B member 4) [NCBI Gene 18670] {aka Mdr2, Pgy-2, Pgy2, mdr-2}, Cacna1s (calcium channel, voltage-dependent, L type, alpha 1S subunit) [NCBI Gene 12292] {aka Cav1.1, Cchl1a3, DHPR, DHPR alpha1s, fmd, mdg}, Orai3 (ORAI calcium release-activated calcium modulator 3) [NCBI Gene 269999] {aka 9930124N15, Tmem142c}, Atp1a1 (ATPase, Na+/K+ transporting, alpha 1 polypeptide) [NCBI Gene 11928] {aka Atpa-1}, Slc12a7 (solute carrier family 12, member 7) [NCBI Gene 20499] {aka D13Ertd261e, Kcc4}, NKA [NCBI Gene 326405], Kcnk1 (potassium channel, subfamily K, member 1) [NCBI Gene 16525] {aka TWIK-1}, SLC25A10 (solute carrier family 25 member 10) [NCBI Gene 1468] {aka DIC, MTDPS19}, GLS (glutaminase) [NCBI Gene 2744] {aka AAD20, CASGID, DEE71, EIEE71, GAC, GAM}, Slc41a1 (solute carrier family 41, member 1) [NCBI Gene 98396] {aka B230315F01Rik}, Itpr1 (inositol 1,4,5-trisphosphate receptor 1) [NCBI Gene 16438] {aka D6Pas2, Gm10429, IP3R 1, IP3R1, InsP3R, Ip3r}, Atp2c2 (ATPase, Ca++ transporting, type 2C, member 2) [NCBI Gene 69047] {aka 1810010G06Rik, Spca2, mKIAA0703}, Trpm7 (transient receptor potential cation channel, subfamily M, member 7) [NCBI Gene 58800] {aka 2310022G15Rik, 4833414K03Rik, 5033407O22Rik, CHAK, CHAK1, LTrpC-7}, PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)) [NCBI Gene 9780] {aka DHS, ER, FAM38A, LMPH3, LMPHM6, Mib}, Mapk8 (mitogen-activated protein kinase 8) [NCBI Gene 26419] {aka JNK, JNK1, Prkm8, SAPK1}
- **Diseases:** Magnesium deficiency (MESH:D008275), Ehlers-Danlos syndrome (MESH:D004535), genetic diseases (MESH:D030342), mineralization defects (MESH:C537337), growth retardation (MESH:D006130), inflammation (MESH:D007249), fracture (MESH:D050723), multidrug (MESH:D018088), osteosarcoma (MESH:D012516), ion channel abnormalities (MESH:C538353), low back pain (MESH:D017116), Alzheimer's disease (MESH:D000544), hypoxic (MESH:D002534), osteoporosis (MESH:D010024), breast cancer (MESH:D001943), calcium dysregulation disorders (MESH:D002128), neurological disorders (MESH:D009461), renal stones (MESH:D007669), periodontitis (MESH:D010518), neurological pathologies (MESH:D005598), Parkinsonism (MESH:D010302), cancer (MESH:D009369), GDD (MESH:C536039), osteolytic destruction (MESH:D008105), blindness (MESH:D001766), glioma (MESH:D005910), autosomal recessive osteopetrosis (MESH:C536059), renal tubular acidosis (MESH:D000141), MLIV (MESH:D009081), hyperalgesia (MESH:D006930), skeletal deformities (MESH:D009140), lysosomal dysfunction (MESH:D016464), OA (MESH:D010003), skeletal abnormalities (MESH:D009139), neurodegeneration (MESH:D019636), osteolysis (MESH:D010014), reperfusion injury (MESH:D015427), diabetes (MESH:D003920), mitochondrial dysfunction (MESH:D028361), Deficiency (MESH:D007153), lipotoxic cardiomyopathy (MESH:D009202), autosomal dominant osteopetrosis type II (MESH:D010022), ischemia (MESH:D007511), hypophosphatasia (MESH:D007014), dental dysplasia (MESH:C536551), bone metabolic diseases (MESH:D001851), bone fragility (MESH:C536063), C1 deficiency (MESH:C565170), cytotoxicity (MESH:D064420), cardiovascular disorders (MESH:D002318), pain (MESH:D010146), intellectual disability (MESH:D008607), bone formation disorders (MESH:D058426), osteoporotic (MESH:D058866), bone defects (MESH:D001847), defective bone resorption (MESH:D001862), iron overload (MESH:D019190), epilepsy (MESH:D004827), diseases (MESH:D004194), bone metastasis (MESH:D009362)
- **Chemicals:** NS8593 (MESH:C515166), indole (MESH:C030374), AMG-517 (MESH:C523409), Glucose (MESH:D005947), MLT (MESH:D008550), cyclic nucleotides (MESH:D009712), Nucleotides (MESH:D009711), acetate (MESH:D000085), Copper (MESH:D003300), Nucleosides (MESH:D009705), phosphonoformic acid (MESH:D017245), Ti6Al4V (MESH:C031462), H2O (MESH:D014867), periplocoside P (MESH:C000599497), saliPhe (MESH:C574373), ZA (MESH:D000077211), cADPR (MESH:D036563), ryanodine (MESH:D012433), ATP (MESH:D000255), metal (MESH:D008670), LPS (MESH:D008070), Vitamin C (MESH:D001205), Thapsigargin (MESH:D019284), CO2 (MESH:D002245), phosphatidylethanolamine (MESH:C483858), HCO3- (MESH:D001639), sulfur (MESH:D013455), UTP (MESH:D014544), flavonoid (MESH:D005419), naringenin (MESH:C005273), diacylglycerol (MESH:D004075), OH- (MESH:C031356), advanced glycation end products (MESH:D017127), phoenixin 20 (MESH:C000705635), amino acid (MESH:D000596), cysteine (MESH:D003545), Pi (MESH:D010716), asparagine (MESH:D001216), luteolin (MESH:D047311), oligomycin A (MESH:C031004), isothiourea (MESH:D013890), H2O2 (MESH:D006861), Glutamate (MESH:D018698), purines (MESH:D011687), RN-1734 (MESH:C544743), hydroxyl radicals (MESH:D017665), BAYK8644 (MESH:D001498), reactive oxygen species (MESH:D017382), proton (MESH:D011522), Cepharanthine (MESH:C006947), AZ11645373 (MESH:C516674), ionomycin (MESH:D015759), macrolide (MESH:D018942), Phosphate (MESH:D010710), fluopicolide (MESH:C557577), carvacrol (MESH:C073316), NAADP (MESH:C024376), Diphyllin (MESH:C010130), ornithine (MESH:D009952), Magnesium (MESH:D008274)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Rattus norvegicus (brown rat, species) [taxon 10116], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Homo sapiens (human, species) [taxon 9606], Gallus gallus (bantam, species) [taxon 9031], Danio rerio (leopard danio, species) [taxon 7955], Mus musculus (house mouse, species) [taxon 10090], Rodentia (rodent, order) [taxon 9989]
- **Mutations:** R444L, alanine/serine, A through H, glutamine to glutamate
- **Cell lines:** RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), MG-63 — Homo sapiens (Human), Osteosarcoma, Cancer cell line (CVCL_0426), 4T1 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_0125)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13031503/full.md

---
Source: https://tomesphere.com/paper/PMC13031503