# Etiology, diagnosis and treatment of lumbar disc degeneration: a focus on the mechanism of action of Piezo1 and research perspectives

**Authors:** Yan Gong, Zhaojun Cheng, Jiahui He, Yanchi Gan, Xiaobing Jiang, Jintao Liu

PMC · DOI: 10.3389/fcell.2026.1679466 · Frontiers in Cell and Developmental Biology · 2026-02-13

## TL;DR

This paper explores how the Piezo1 ion channel contributes to lumbar disc degeneration and suggests new treatment strategies based on its role in sensing mechanical stress.

## Contribution

The paper systematically reviews Piezo1's role in lumbar disc degeneration and proposes it as a target for new prevention and treatment strategies.

## Key findings

- Piezo1 senses abnormal mechanical stress and mediates Ca2+ influx in degenerating discs.
- Piezo1 activation triggers inflammation and inhibits extracellular matrix synthesis.
- Elevated Piezo1 activity in degenerated discs links mechanical signals to pathological processes.

## Abstract

Lumbar disc degeneration (LDD) is a chronic degenerative disease caused by the interaction of genetic and environmental factors, which mainly leads to lower back pain. Its early-stage lesions are insidious and lack reliable biomarkers, and the current diagnosis relies on imaging. Piezo1, a mechanosensitive ion channel widely expressed by intervertebral disc cells, is a core molecule that senses mechanical signals. As a core load-bearing structure of the spine, the mechanical responsiveness of the intervertebral disc is critical for homeostasis, and abnormal mechanical loading is a key trigger of LDD. Piezo1 is deeply involved in the pathology of LDD by sensing abnormal stress and mediating Ca2+ influx. On the one hand, activation of the Piezo1-Ca2+ axis triggers inflammatory pathways such as NF-κB and the upregulation of proinflammatory factors and matrix-degrading enzymes (e.g., MMPs, ADAMTS); on the other hand, it inhibits the synthesis of the extracellular matrix (ECM), such as type II collagen and proteoglycans, and promotes apoptosis and senescence. The “hypersensitive state” of degenerated discs, in which Piezo1 expression and activity are significantly elevated, is the core link between the transduction and amplification of mechanical signals and pathological cascades. By systematically reviewing the structure and function of Piezo1 and its regulatory mechanism in LDD, we aimed to clarify its role as a core mechanosensing molecule in degeneration and provide theoretical basis for new prevention and treatment strategies.

## Linked entities

- **Genes:** PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)) [NCBI Gene 9780]
- **Proteins:** PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)), NFKB1 (nuclear factor kappa B subunit 1), adamts (a disintegrin-like and metallopeptidase with thrombospondin type 1 motif)
- **Chemicals:** Ca2+ (PubChem CID 271)
- **Diseases:** lumbar disc degeneration (MONDO:0011385)

## Full-text entities

- **Genes:** CASP1 (caspase 1) [NCBI Gene 834] {aka ICE, IL1BC, P45}, TRPV4 (transient receptor potential cation channel subfamily V member 4) [NCBI Gene 59341] {aka BCYM3, CMT2C, HMSN2C, OTRPC4, SMAL, SPSMA}, YAP1 (Yes1 associated transcriptional regulator) [NCBI Gene 10413] {aka COB1, YAP, YAP-1, YAP2, YAP65, YKI}, Selenok (selenoprotein K) [NCBI Gene 80795] {aka 1110001C03Rik, HSPC030, Hsp30, Selk}, Casp3 (caspase 3) [NCBI Gene 25402] {aka CPP32-beta, Lice, Yama}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, TAC1 (tachykinin precursor 1) [NCBI Gene 6863] {aka Hs.2563, NK2, NKNA, NPK, TAC2}, ACAN (aggrecan) [NCBI Gene 176] {aka AGC1, AGCAN, CSPG1, CSPGCP, MSK16, SEDK}, Bax (BCL2 associated X, apoptosis regulator) [NCBI Gene 24887], COL2A1 (collagen type II alpha 1 chain) [NCBI Gene 1280] {aka ACG2, ANFH, ANFH1, AOM, COL11A3, EDMMD}, Piezo1 (piezo-type mechanosensitive ion channel component 1) [NCBI Gene 234839] {aka 9630020g22, Fam38a, mKIAA0233}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, DCN (decorin) [NCBI Gene 1634] {aka CSCD, DSPG2, PG40, PGII, PGS2, SLRR1B}, DAPK2 (death associated protein kinase 2) [NCBI Gene 23604] {aka DRP-1, DRP1}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, PYCARD (PYD and CARD domain containing) [NCBI Gene 29108] {aka ASC, CARD5, TMS, TMS-1, TMS1}, Gpx4 (glutathione peroxidase 4) [NCBI Gene 625249] {aka GPx-4, GSHPx-4, PHGPx, mtPHGPx, snGPx}, HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, PIEZO2 (piezo type mechanosensitive ion channel component 2) [NCBI Gene 63895] {aka C18orf30, C18orf58, DA3, DA5, DAIPT, FAM38B}, CAMK2G (calcium/calmodulin dependent protein kinase II gamma) [NCBI Gene 818] {aka CAMK, CAMK-II, CAMKG, MRD59}, MMP13 (matrix metallopeptidase 13) [NCBI Gene 4322] {aka CLG3, MANDP1, MDST, MMP-13}, COL9A2 (collagen type IX alpha 2 chain) [NCBI Gene 1298] {aka DJ39G22.4, EDM2, MED, STL5}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, Nlrp3 (NLR family, pyrin domain containing 3) [NCBI Gene 287362] {aka Cias1}, TFRC (transferrin receptor) [NCBI Gene 7037] {aka CD71, IMD46, T9, TFR, TFR1, TR}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)) [NCBI Gene 9780] {aka DHS, ER, FAM38A, LMPH3, LMPHM6, Mib}, COL11A1 (collagen type XI alpha 1 chain) [NCBI Gene 1301] {aka CO11A1, COLL6, DFNA37, STL2}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Piezo1 (piezo-type mechanosensitive ion channel component 1) [NCBI Gene 361430] {aka Fam38a, Mib}, MMP3 (matrix metallopeptidase 3) [NCBI Gene 4314] {aka CHDS6, MMP-3, SL-1, STMY, STMY1, STR1}, Capn2 (calpain 2) [NCBI Gene 29154], Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}
- **Diseases:** spinal trauma (MESH:D013119), sensory abnormalities (MESH:D012678), weakness (MESH:D018908), ischemic (MESH:D002545), disc water loss (MESH:D000069578), spinal disorder (MESH:D013118), vertebral fractures (MESH:C535781), cancer (MESH:D009369), calcification (MESH:D002114), mechanical injury (MESH:D041781), motor deficits (MESH:D009461), stenosis (MESH:D003251), liver cancer (MESH:D006528), herniation (MESH:D004677), infections (MESH:D007239), osteoarthritis (MESH:D010003), cardiovascular developmental disorders (MESH:D002318), gastrointestinal ulcers (MESH:D014456), chronic kidney disease fibrosis (MESH:D051436), CEP (MESH:D002357), edema (MESH:D004487), neurogenic claudication (MESH:D007383), ECM synthesis (MESH:C535509), radiculopathy (MESH:D011843), numbness (MESH:D006987), damage (MESH:D020263), lumbar instability (MESH:C563613), NP (MESH:C537927), hypertensive nephropathy (MESH:C563161), dehydration (MESH:D003681), NPC (MESH:D052556), impact injury (MESH:D004834), disc herniation (MESH:D007405), spinal stenosis (MESH:D013130), Low back pain (MESH:D017116), disability (MESH:D009069), prostate cancer (MESH:D011471), structural degeneration (MESH:D020914), AF (OMIM:614822), stomach cancer (MESH:D013274), disc dysfunction (MESH:D009901), HS (MESH:D013103), abnormalities of the cauda equina (MESH:D011128), hypoxic (MESH:D002534), disc degeneration (MESH:D055959), Obesity (MESH:D009765), urinary and fecal dysfunction (MESH:D005242), breast cancer (MESH:D001943), abnormalities (MESH:D000014), calcium (MESH:D002128), trauma (MESH:D014947), degenerative disease (MESH:D019636), orthopedic diseases (MESH:D009140), DDD (MESH:C562924), sclerosis (MESH:D012598), iron metabolism disorders (MESH:D019189), endplate calcification (MESH:C566415), inflammation (MESH:D007249), nerve damage (MESH:D000080902), paraspinal tenderness (MESH:D063806)
- **Chemicals:** prostaglandins (MESH:D011453), carbon monoxide (MESH:D002248), lipid peroxides (MESH:D008054), Nicotine (MESH:D009538), Selenium (MESH:D012643), Calcium (MESH:D002118), selenocysteine (MESH:D017279), ROS (MESH:D017382), Mdivi-1 (MESH:C000723896), glutathione (MESH:D005978), BAPTA-AM (MESH:C070379), KN-93 (MESH:C072105), Ca2+ (-), water (MESH:D014867), ATP (MESH:D000255), Na+ (MESH:D012964), oxygen (MESH:D010100), LPS (MESH:D008070), lipid (MESH:D008055), K+ (MESH:D011188), salt (MESH:D012492), Iron (MESH:D007501)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]
- **Mutations:** S152994302500302X

## Full text

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## Figures

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## References

123 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946040/full.md

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Source: https://tomesphere.com/paper/PMC12946040