# Vitamin D-Mediated Immunoregulation in Degenerative Diseases: Insights into Cardiovascular, Neurodegenerative and Musculoskeletal Disorders

**Authors:** Ga Young Lee, Chan Yoon Park, Sung Nim Han

PMC · DOI: 10.3390/nu18040629 · Nutrients · 2026-02-14

## TL;DR

This review explores how vitamin D influences immune and metabolic processes in degenerative diseases like heart, brain, and muscle disorders.

## Contribution

The paper provides a comprehensive overview of vitamin D's immunoregulatory roles in degenerative diseases.

## Key findings

- Vitamin D modulates neuronal survival and synaptic plasticity through genomic and non-genomic mechanisms.
- Vitamin D regulates brain inflammation and oxidative stress via microglial and astrocytic responses.
- Vitamin D supports bone-muscle homeostasis and mitochondrial function while reducing oxidative stress.

## Abstract

Degenerative diseases are characterized by the gradual loss of cellular integrity, tissue function, and regenerative capacity. Cardiovascular diseases, neurodegenerative disorders, and musculoskeletal deterioration are considered major categories of degenerative diseases, and vitamin D deficiency has been linked with an increased risk of these conditions. Vitamin D has the potential to modulate neurogenerative process by influencing the progression of neuronal survival, neurogenesis, and synaptic plasticity through both genomic and non-genomic mechanisms mediated by vitamin D receptors, which are widely distributed across brain regions and cell types. Additionally, vitamin D regulates brain immunometabolism by modulating microglial and astrocytic inflammatory responses and oxidative stress. Vitamin D has long been recognized as essential for bone health. Beyond its classical role, vitamin D contributes to the maintenance of bone–muscle homeostasis, enhances mitochondrial biogenesis and ATP production while reducing oxidative stress, and facilitates bidirectional bone–muscle crosstalk through myokines and osteokines to coordinate bone remodeling and muscle regeneration. However, despite these mechanistic insights, the beneficial effects of vitamin D on these diseases—such as reduced risk or mitigation of progression—remains inconclusive. This review explores the relationships between vitamin D and cardiovascular, neurodegenerative, and musculoskeletal diseases, with a focus on the underlying immunological and metabolic mechanisms of actions.

## Full-text entities

- **Genes:** TLR2 (toll like receptor 2) [NCBI Gene 7097] {aka CD282, TIL4}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Dnm1l (dynamin 1-like) [NCBI Gene 74006] {aka 6330417M19Rik, Dlp1, Dnmlp1, Drp1, python}, NT-3 [NCBI Gene 4877], PVALB (parvalbumin) [NCBI Gene 5816] {aka D22S749}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, CYP27A1 (cytochrome P450 family 27 subfamily A member 1) [NCBI Gene 1593] {aka CP27, CTX, CYP27}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, Psen1 (presenilin 1) [NCBI Gene 19164] {aka Ad3h, PS-1, PS1, S182}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}, TNFSF11 (TNF superfamily member 11) [NCBI Gene 8600] {aka CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B}, FBXO32 (F-box protein 32) [NCBI Gene 114907] {aka Fbx32, MAFbx}, CNTF (ciliary neurotrophic factor) [NCBI Gene 1270] {aka HCNTF}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, NTF3 (neurotrophin 3) [NCBI Gene 4908] {aka HDNF, NGF-2, NGF2, NT-3, NT3}, Foxo1 (forkhead box O1) [NCBI Gene 56458] {aka Afxh, FKHR, Fkhr1, Foxo1a}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, Pgp (phosphoglycolate phosphatase) [NCBI Gene 67078] {aka 1700012G19Rik, AUM, G3PP}, KL (klotho) [NCBI Gene 9365] {aka HFTC3, KLA}, VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 22339] {aka L-VEGF, Vegf, Vpf}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, Nos2 (nitric oxide synthase 2, inducible) [NCBI Gene 18126] {aka MAC-NOS, NOS-II, Nos-2, Nos2a, i-NOS, iNOS}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, PDIA3 (protein disulfide isomerase family A member 3) [NCBI Gene 2923] {aka ER60, ERp57, ERp60, ERp61, GRP57, GRP58}, PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476] {aka BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Map2 (microtubule-associated protein 2) [NCBI Gene 25595] {aka MAP2R, Mtap2}, PAX7 (paired box 7) [NCBI Gene 5081] {aka CMYO19, CMYP19, HUP1, MYOSCO, PAX7B, RMS2}, TH (tyrosine hydroxylase) [NCBI Gene 7054] {aka DYT14, DYT5b, TYH}, TRIM63 (tripartite motif containing 63) [NCBI Gene 84676] {aka CMH31, IRF, MURF1, MURF2, RNF28, SMRZ}, WNT3A (Wnt family member 3A) [NCBI Gene 89780], NGF (nerve growth factor) [NCBI Gene 4803] {aka Beta-NGF, HSAN5, NGFB}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}, RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970] {aka AIF3BL3, CMCU, NFKB3, p65}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, Bace1 (beta-site APP cleaving enzyme 1) [NCBI Gene 23821] {aka ASP2, Bace}, CYP24A1 (cytochrome P450 family 24 subfamily A member 1) [NCBI Gene 1591] {aka CP24, CYP24, HCAI, HCINF1, P450-CC24}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, FNDC5 (fibronectin type III domain containing 5) [NCBI Gene 252995] {aka FRCP2, irisin}, COMT (catechol-O-methyltransferase) [NCBI Gene 1312] {aka HEL-S-98n}, Pth (parathyroid hormone) [NCBI Gene 19226] {aka Pthp}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, TLR9 (toll like receptor 9) [NCBI Gene 54106] {aka CD289}, ITGAM (integrin subunit alpha M) [NCBI Gene 3684] {aka CD11B, CR3A, HNA-4, MAC-1, MAC1A, MO1A}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, PSEN1 (presenilin 1) [NCBI Gene 5663] {aka ACNINV3, AD3, CMD1U, FAD, PS-1, PS1}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, Mrc1 (mannose receptor, C type 1) [NCBI Gene 17533] {aka CD206, MR}
- **Diseases:** Neurodegenerative Diseases (MESH:D019636), injury to (MESH:D014947), vascular calcification (MESH:D061205), Sarcopenia (MESH:D055948), inflammation (MESH:D007249), muscle atrophy (MESH:D009133), glioma (MESH:D005910), ALS (MESH:D000690), hypertensive (MESH:D006973), sleep disorders (MESH:D012893), transverse myelitis (MESH:D009188), pain (MESH:D010146), fracture (MESH:D050723), impaired physical performance (MESH:D059445), axonal and myelin injury (MESH:D003711), death (MESH:D003643), PD (MESH:D010300), muscle (MESH:D019042), tremor (MESH:D014202), viral infections (MESH:D014777), mitochondrial dysfunction (MESH:D028361), atherosclerosis (MESH:D050197), acute myocardial infarction (MESH:D009203), MCI (MESH:D060825), AD (MESH:D000544), behavioral impairments (MESH:D001523), optic neuritis (MESH:D009902), arterial dilation (MESH:D002311), brainstem syndromes (MESH:D020295), neurotoxicity (MESH:D020258), CVD (MESH:D002318), skeletal disorders (MESH:C564967), hypertrophy (MESH:D006984), endothelial dysfunction (MESH:D014652), muscle weakness (MESH:D018908), cancer (MESH:D009369), hypercalcemia (MESH:D006934), Dysfunction of vascular endothelium (MESH:D002561), bone (MESH:D001847), ossification (MESH:C562735), Osteoporosis (MESH:D010024), CKD (MESH:D051436), schizophrenia (MESH:D012559), neuroinflammation (MESH:D000090862), atrophy (MESH:D001284), inflammatory cytokines (MESH:D000080424), degeneration of dopaminergic neurons (MESH:D009410), Musculoskeletal Disorders (MESH:D009140), reduced BMD (MESH:D001851), gait disturbances (MESH:D020233), obesity (MESH:D009765), EAE (MESH:D004681), paralysis (MESH:D010243), impaired muscle function (MESH:D009135), CAC (MESH:D003324), amyloid (MESH:C000718787), Dementia (MESH:D003704), Lewy (MESH:D018827), stroke (MESH:D020521), Vitamin D (MESH:D014808)
- **Chemicals:** 25(OH)D (-), calcipotriol (MESH:C055085), Vitamin D (MESH:D014807), L-DOPA (MESH:D007980), 25-hydroxyvitamin D (MESH:C104450), phosphorus (MESH:D010758), phosphate (MESH:D010710), oxygen (MESH:D010100), Vitamin D3 (MESH:D002762), ATP (MESH:D000255), rotenone (MESH:D012402), 6-OHDA (MESH:D016627), LPS (MESH:D008070), acetylcholine (MESH:D000109), dopamine (MESH:D004298), 1,25(OH)2D3 (MESH:D002117), 1alpha-hydroxycholecalciferol (MESH:C008088), glutamate (MESH:D018698), NO (MESH:D009569), 1,25(OH)2D (MESH:C097949), calcium (MESH:D002118), ROS (MESH:D017382)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** C2C12 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0188), SH-SY5Y — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_0019), VSMC — Homo sapiens (Human), Finite cell line (CVCL_4009)

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## References

220 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942877/full.md

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Source: https://tomesphere.com/paper/PMC12942877