# Ion Channel Integration and Functional Coupling in Salivary Gland Fluid Secretion

**Authors:** Tarek Mohamed Abd El-Aziz, Brij B. Singh

PMC · DOI: 10.3390/cells15040369 · 2026-02-19

## TL;DR

This paper explains how ion channels work together in salivary glands to produce saliva through coordinated cellular processes.

## Contribution

The paper provides a unified framework of ion channel integration in salivary fluid secretion under physiological conditions.

## Key findings

- Salivary fluid secretion involves two stages: isotonic secretion by acinar cells and ionic modification in ductal epithelium.
- Calcium signaling activates chloride channels and potassium channels, which are critical for fluid secretion.
- Ion transport pathways in ductal epithelium modify primary saliva to produce hypotonic final saliva.

## Abstract

Salivary glands produce saliva through precisely coordinated epithelial ion transport processes. Ion channels are essential components of the molecular machinery that convert neural and hormonal signals into targeted ion and water flux. This review focuses on the integrated molecular and cellular mechanisms by which ion channels cooperate to generate salivary fluid under physiological conditions. Saliva formation proceeds through two sequential stages: isotonic primary fluid secretion by acinar cells, followed by ionic modification within the ductal epithelium. Parasympathetic stimulation activates muscarinic M1/3 receptors, initiating intracellular calcium signaling through inositol 1,4,5-trisphosphate-dependent release from the endoplasmic reticulum and sustained calcium entry via Orai1/TRPC channels. Elevated cytosolic calcium activates apical ANO1/TMEM16A chloride channels, the rate-limiting step in acinar fluid secretion, together with basolateral calcium-activated potassium channels that preserve the electrochemical driving force for chloride efflux. Chloride accumulation is maintained by Na+/K+-ATPase and the Na+-K+-2Cl− cotransporter, while osmotic gradients drive water movement through apical aquaporin-5 and basolateral aquaporin-1/3. As primary saliva traverses the ductal system, epithelial sodium channels, CFTR, and additional ion transport pathways reabsorb sodium and chloride and secrete potassium and bicarbonate, producing hypotonic final saliva. By synthesizing calcium signaling, chloride and potassium conductance, sodium handling, and epithelial polarity into a unified framework, this review establishes ion channel integration as the fundamental basis of salivary gland fluid secretion.

## Linked entities

- **Genes:** ANO1 (anoctamin 1) [NCBI Gene 55107], ANO1 (anoctamin 1) [NCBI Gene 55107], ORAI1 (ORAI calcium release-activated calcium modulator 1) [NCBI Gene 84876], trpC (indole-3-glycerol phosphate synthase) [NCBI Gene 882120], nrv1 (nervana 1) [NCBI Gene 33952], CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080], AQP5 (aquaporin 5) [NCBI Gene 431305]
- **Chemicals:** calcium (PubChem CID 5460341), chloride (PubChem CID 312), potassium (PubChem CID 813), sodium (PubChem CID 5360545), bicarbonate (PubChem CID 769), inositol 1,4,5-trisphosphate (PubChem CID 439456)

## Full-text entities

- **Genes:** Scnn1a (sodium channel, nonvoltage-gated 1 alpha) [NCBI Gene 20276] {aka ENaC, SCNEA, Scnn1, mENaC}, CLC [NCBI Gene 12735], Aqp3 (aquaporin 3) [NCBI Gene 11828] {aka AQP-2}, Trpc3 (transient receptor potential cation channel, subfamily C, member 3) [NCBI Gene 22065] {aka Mwk, Trcp3, Trp3, Trrp3}, Cftr (cystic fibrosis transmembrane conductance regulator) [NCBI Gene 12638] {aka Abcc7}, Slc9a3 (solute carrier family 9 (sodium/hydrogen exchanger), member 3) [NCBI Gene 105243] {aka 9030624O13Rik, NHE-3, NHE3}, Itpr3 (inositol 1,4,5-triphosphate receptor 3) [NCBI Gene 16440] {aka IP3R 3, IP3R-3, Ip3r3, Itpr-3, tf}, Stim1 (stromal interaction molecule 1) [NCBI Gene 20866] {aka SIM}, Ano1 (anoctamin 1, calcium activated chloride channel) [NCBI Gene 101772] {aka Tmem16a}, ITPR2 (inositol 1,4,5-trisphosphate receptor type 2) [NCBI Gene 3709] {aka ANHD, CFAP48, INSP3R2, IP3R2}, Itpr1 (inositol 1,4,5-trisphosphate receptor 1) [NCBI Gene 16438] {aka D6Pas2, Gm10429, IP3R 1, IP3R1, InsP3R, Ip3r}, Creb1 (cAMP responsive element binding protein 1) [NCBI Gene 12912] {aka 2310001E10Rik, 3526402H21Rik, Creb, Creb-1}, P2rx7 (purinergic receptor P2X, ligand-gated ion channel, 7) [NCBI Gene 18439] {aka P2X(7), P2X7R}, Brp1 (brain protein 1) [NCBI Gene 109667] {aka A1, Brp-1}, AQP1 (aquaporin 1 (Colton blood group)) [NCBI Gene 358] {aka AQP-CHIP, CHIP28, CO}, Ryr1 (ryanodine receptor 1, skeletal muscle) [NCBI Gene 20190] {aka RYR-1, Ryr, skrr}, Lrrc8a (leucine rich repeat containing 8A VRAC subunit A) [NCBI Gene 241296] {aka Lrrc8, SWELL1, ebo, mKIAA1437}, Ryr2 (ryanodine receptor 2, cardiac) [NCBI Gene 20191] {aka 9330127I20Rik, RYR-2}, Cacna1c (calcium channel, voltage-dependent, L type, alpha 1C subunit) [NCBI Gene 12288] {aka Cav1.2, Cchl1a1, D930026N18Rik, MBC, MELC-CC}, Piezo1 (piezo-type mechanosensitive ion channel component 1) [NCBI Gene 234839] {aka 9630020g22, Fam38a, mKIAA0233}, Kcnj2 (potassium inwardly-rectifying channel, subfamily J, member 2) [NCBI Gene 16518] {aka IRK1, Kcnf1, Kir2.1}, Gast (gastrin) [NCBI Gene 14459] {aka GAS}, Gnaq (guanine nucleotide binding protein, alpha q polypeptide) [NCBI Gene 14682] {aka 1110005L02Rik, 6230401I02Rik, Dsk1, Dsk10, Galphaq, Gq}, Aqp5 (aquaporin 5) [NCBI Gene 11830], Camk2b (calcium/calmodulin-dependent protein kinase II, beta) [NCBI Gene 12323] {aka CaMKII}, Camp (cathelicidin antimicrobial peptide) [NCBI Gene 12796] {aka CAP18, CLP, Cnlp, Cramp, FALL39, MCLP}, Ezr (ezrin) [NCBI Gene 22350] {aka Vil2, p81}, Sgk1 (serum/glucocorticoid regulated kinase 1) [NCBI Gene 20393] {aka Sgk}, Orai1 (ORAI calcium release-activated calcium modulator 1) [NCBI Gene 109305] {aka D730049H07Rik, Tmem142a, orai-1}, Slc4a4 (solute carrier family 4 (anion exchanger), member 4) [NCBI Gene 54403] {aka NBC, NBC1}, Aqp1 (aquaporin 1) [NCBI Gene 11826] {aka CHIP28}, EZR (ezrin) [NCBI Gene 7430] {aka CVIL, CVL, HEL-S-105, VIL2}, SLC12A1 (solute carrier family 12 member 1) [NCBI Gene 6557] {aka BSC, BSC-1, BSC1, CCC2, NKCC2}, Itpr2 (inositol 1,4,5-triphosphate receptor 2) [NCBI Gene 16439] {aka InsP3R-2, InsP3R-5, Ip3r2, Itpr5, insP3R2}, Nos1 (nitric oxide synthase 1, neuronal) [NCBI Gene 18125] {aka 2310005C01Rik, N-NOS, NC-NOS, NO, NOS, NOS-I}, Kcnma1 (potassium large conductance calcium-activated channel, subfamily M, alpha member 1) [NCBI Gene 16531] {aka 5730414M22Rik, BKCA alpha, BKCa, KCa1.1, MaxiK, Slo}, Mapk1 (mitogen-activated protein kinase 1) [NCBI Gene 26413] {aka 9030612K14Rik, ERK, Erk2, MAPK2, PRKM2, Prkm1}, Slc4a9 (solute carrier family 4, sodium bicarbonate cotransporter, member 9) [NCBI Gene 240215] {aka AE 4, AE4, D630003B07, D630024F24Rik}, AQP5 (aquaporin 5) [NCBI Gene 362] {aka AQP-5, PPKB}, Lrpap1 (low density lipoprotein receptor-related protein associated protein 1) [NCBI Gene 16976] {aka HBP44, RAP}, Slc9a1 (solute carrier family 9 (sodium/hydrogen exchanger), member 1) [NCBI Gene 20544] {aka Apnh, Mir5122, Nhe1, mir-5122, swe}, Syt17 (synaptotagmin XVII) [NCBI Gene 110058] {aka Bk, sytXVII}, Slc4a2 (solute carrier family 4 (anion exchanger), member 2) [NCBI Gene 20535] {aka Ae2, B3RP}, Slc9a2 (solute carrier family 9 (sodium/hydrogen exchanger), member 2) [NCBI Gene 226999] {aka 2210416H12Rik, 4932415O19Rik, NHE-2, NHE2}, Trpm2 (transient receptor potential cation channel, subfamily M, member 2) [NCBI Gene 28240] {aka 9830168K16Rik, LTRPC2, TRPC7, Trp7, Trrp7}, CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}, Ahcyl1 (S-adenosylhomocysteine hydrolase-like 1) [NCBI Gene 229709] {aka 1110034F20Rik, Ahcy-rs3, DCAL, Irbit}, Calm2 (calmodulin 2) [NCBI Gene 12314] {aka 1500001E21Rik, Cam2, CamC}, Casr (calcium-sensing receptor) [NCBI Gene 12374] {aka CaR, Gprc2a}, ITPR1 (inositol 1,4,5-trisphosphate receptor type 1) [NCBI Gene 3708] {aka ACV, CLA4, INSP3R1, IP3R, IP3R1, PPP1R94}, Plcb3 (phospholipase C, beta 3) [NCBI Gene 18797] {aka mKIAA4098}, mucin [NCBI Gene 100508689], Aqp4 (aquaporin 4) [NCBI Gene 11829] {aka WCH4}, Clcn3 (chloride channel, voltage-sensitive 3) [NCBI Gene 12725] {aka Clc3}, Slc12a2 (solute carrier family 12, member 2) [NCBI Gene 20496] {aka 9330166H04Rik, BSC2, Nkcc1, mBSC2, mNKCC1, sy-ns}, Trpv3 (transient receptor potential cation channel, subfamily V, member 3) [NCBI Gene 246788] {aka 1110036I10Rik, Nh, VRL3}, Rapgef3 (Rap guanine nucleotide exchange factor (GEF) 3) [NCBI Gene 223864] {aka 2310016P22Rik, 9330170P05Rik, Epac, Epac1}, St3gal5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5) [NCBI Gene 20454] {aka 3S-T, Siat9, [a]2}, Prkca (protein kinase C, alpha) [NCBI Gene 18750] {aka Pkca}, Tac1 (tachykinin 1) [NCBI Gene 21333] {aka 4930528L02Rik, NK-1, NK1, Nkna, PPT-A, PPTA}
- **Diseases:** Xerostomia (MESH:D014987), Radiation injury (MESH:D011832), sialolithiasis (MESH:D015494), autoimmune destruction (MESH:D008105), RVD (MESH:D009123), dental caries (MESH:D003731), NKCC1 deficiency (MESH:D014813), salivary (MESH:D012466), oral infections (MESH:D007239), autoimmune disease (MESH:D001327), mitochondrial dysfunction (MESH:D028361), growth impairment (MESH:D006130), inflammatory (MESH:D007249), injury to (MESH:D014947), swelling (MESH:D004487), CF (MESH:D003550), head and neck cancers (MESH:D006258), Sjogren's syndrome (MESH:D012859), water channel abnormalities (MESH:D000069578), salivary gland hypofunction (MESH:D000309), deafness (MESH:D003638)
- **Chemicals:** ruthenium red (MESH:D012430), lipid (MESH:D008055), Capsaicin (MESH:D002211), ouabain (MESH:D010042), ATP (MESH:D000255), CFTRinh-172 (MESH:C482900), isoproterenol (MESH:D007545), ROS (MESH:D017382), Calcium (MESH:D002118), ryanodine (MESH:D012433), heparin (MESH:D006493), H+ (MESH:D006859), DAG (MESH:D004075), amiloride (MESH:D000584), pilocarpine (MESH:D010862), glycerol (MESH:D005990), caffeine (MESH:D002110), Na+ (MESH:D012964), K+ (MESH:D011188), NO (MESH:D009614), 3Na+ (-), Bicarbonate (MESH:D001639), piperine (MESH:C008922), Cl- (MESH:D002713), MitoTEMPO (MESH:C555916), forskolin (MESH:D005576), urea (MESH:D014508), RU486 (MESH:D015735), Acetylcholine (MESH:D000109), cardiac glycoside (MESH:D002301), luminal (MESH:D010634), Water (MESH:D014867), IP3 (MESH:D015544), Chloride (MESH:D002712), Cyclic adenosine monophosphate (MESH:D000242), Nitric Oxide (MESH:D009569), GDP (MESH:D006153), noradrenaline (MESH:D009638), ADP-ribose (MESH:D000246), BK (MESH:D001603), salt (MESH:D012492), NaCl (MESH:D012965), cGMP (MESH:D006152), carbachol (MESH:D002217), cADPR (MESH:D036563), guanine (MESH:D006147), PIP2 (MESH:D019269), nifedipine (MESH:D009543), Hydrocortisone (MESH:D006854), acetazolamide (MESH:D000086)
- **Species:** Bos taurus (bovine, species) [taxon 9913], Homo sapiens (human, species) [taxon 9606], Rodentia (rodent, order) [taxon 9989], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939591/full.md

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Source: https://tomesphere.com/paper/PMC12939591