# Emerging frontiers in the mitochondrial regulation of dendritic cell biology

**Authors:** B. Chen, J.U. Mayer

PMC · DOI: 10.1016/j.redox.2026.104032 · 2026-01-14

## TL;DR

This paper explores how mitochondria regulate dendritic cells, which are crucial for immune responses, and suggests targeting mitochondrial pathways could improve immune health in aging and disease.

## Contribution

The paper reviews emerging evidence that mitochondrial regulation influences dendritic cell biology and proposes targeting these pathways as a novel therapeutic strategy.

## Key findings

- Mitochondrial pathways affect dendritic cell differentiation and activation.
- Mitochondrial dysfunction is linked to impaired dendritic cell function in aging and disease.
- Targeting mitochondrial and redox pathways could restore immune competence.

## Abstract

Dendritic Cells are central players of our immune system, linking innate sensing to adaptive immunity through antigen presentation and T cell priming. Beyond transcriptional and cytokine-based regulation, mitochondria are emerging as potential regulators of Dendritic Cell biology. While still in its infancy, evidence is accumulating that mitochondrial pathways affect Dendritic Cell differentiation; that mitochondrial remodeling and bioenergetic rewiring underpin Dendritic Cell maturation and activation in response to pathogenic and inflammatory stimuli and that shifts in mitochondrial and redox dynamics, reactive oxygen species production and mitochondrial DNA release coincide with Dendritic Cell activation and co-stimulatory molecule expression. Mitochondria are furthermore involved in regulating Dendritic Cell migration by influencing cellular metabolism and cytoskeletal dynamics and support the antigen processing and presentation machinery, thereby dictating the quality of the initiated T cell response. Importantly, mitochondrial checkpoints also regulate Dendritic Cell survival, balancing immune activation with timely cell death to preserve immune homeostasis.

While the exact pathways of mitochondrial regulation are just beginning to be understood, disruptions in these programs can be far reaching. During aging, progressive mitochondrial dysfunction has been associated with impaired Dendritic Cell differentiation, diminished antigen presentation and impaired T cell responses. Similar defects have been observed in chronic diseases and cancer, leading us to hypothesize that genetic disorders linked to mitochondrial dysfunction also lead to defects in Dendritic Cell biology, impacting clinical symptoms such as immune dysregulation, heightened infection risk and inappropriate chronic inflammation.

Therefore, in this review we have summarized the emerging roles of mitochondrial regulation in Dendritic Cell biology and discuss therapeutic opportunities to restore immune competence by targeting mitochondrial and redox pathways in settings of Dendritic Cell dysfunction. These insights aim to encourage further research into these topics and propose targeted metabolic reprogramming as a new therapeutic strategy for healthy ageing and chronic disease management.

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## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** Bak1 (BCL2-antagonist/killer 1) [NCBI Gene 12018] {aka Bak, N-BAK1, N-Bak}, CD69 (CD69 molecule) [NCBI Gene 969] {aka AIM, BL-AC/P26, CLEC2C, EA1, GP32/28, MLR-3}, CD80 (CD80 molecule) [NCBI Gene 941] {aka B7, B7-1, B7.1, BB1, CD28LG, CD28LG1}, ATM (ATM serine/threonine kinase) [NCBI Gene 472] {aka AT1, ATA, ATC, ATD, ATDC, ATE}, TFAM (transcription factor A, mitochondrial) [NCBI Gene 7019] {aka MTDPS15, MTTF1, MTTFA, TCF6, TCF6L1, TCF6L2}, MYCL (MYCL proto-oncogene, bHLH transcription factor) [NCBI Gene 4610] {aka L-Myc, LMYC, MYCL1, bHLHe38}, BAK1 (BCL2 antagonist/killer 1) [NCBI Gene 578] {aka BAK, BAK-LIKE, BCL2L7, CDN1}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, HK2 (hexokinase 2) [NCBI Gene 3099] {aka HKII, HXK2}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, NRF1 (nuclear respiratory factor 1) [NCBI Gene 4899] {aka ALPHA-PAL}, PINK1 (PTEN induced kinase 1) [NCBI Gene 65018] {aka BRPK, PARK6}, ITGAM (integrin subunit alpha M) [NCBI Gene 3684] {aka CD11B, CR3A, HNA-4, MAC-1, MAC1A, MO1A}, TLR9 (toll like receptor 9) [NCBI Gene 54106] {aka CD289}, IFNB1 (interferon beta 1) [NCBI Gene 3456] {aka IFB, IFF, IFN-beta, IFNB}, PDC (phosducin) [NCBI Gene 5132] {aka MEKA, PHD, PhLOP, PhLP}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}, Casp8 (caspase 8) [NCBI Gene 12370] {aka CASP-8, FLICE, MACH, Mch5}, CCR7 (C-C motif chemokine receptor 7) [NCBI Gene 1236] {aka BLR2, CC-CKR-7, CCR-7, CD197, CDw197, CMKBR7}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CS (citrate synthase) [NCBI Gene 1431], PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, CYCS (cytochrome c, somatic) [NCBI Gene 54205] {aka CYC, HCS, THC4}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, CCL19 (C-C motif chemokine ligand 19) [NCBI Gene 6363] {aka CKb11, ELC, MIP-3b, MIP3B, SCYA19}, CLEC9A (C-type lectin domain containing 9A) [NCBI Gene 283420] {aka CD370, DNGR-1, DNGR1, UNQ9341}, TRIM63 (tripartite motif containing 63) [NCBI Gene 84676] {aka CMH31, IRF, MURF1, MURF2, RNF28, SMRZ}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, KMO (kynurenine 3-monooxygenase) [NCBI Gene 8564] {aka dJ317G22.1}, CLEC4C (C-type lectin domain family 4 member C) [NCBI Gene 170482] {aka BDCA-2, BDCA2, CD303, CLECSF11, CLECSF7, DLEC}, APAF1 (apoptotic peptidase activating factor 1) [NCBI Gene 317] {aka APAF-1, CED4}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, IRF8 (interferon regulatory factor 8) [NCBI Gene 3394] {aka H-ICSBP, ICSBP, ICSBP1, IMD32A, IMD32B, IRF-8}, Fas (Fas cell surface death receptor) [NCBI Gene 14102] {aka APO1, APT1, CD95, TNFR6, Tnfrsf6, lpr}, BCL2L11 (BCL2 like 11) [NCBI Gene 10018] {aka BAM, BIM, BOD}, TNFRSF4 (TNF receptor superfamily member 4) [NCBI Gene 7293] {aka ACT35, CD134, IMD16, OX40, TXGP1L}, Hif1a (hypoxia inducible factor 1, alpha subunit) [NCBI Gene 15251] {aka HIF-1-alpha, HIF1-alpha, HIF1alpha, MOP1, bHLHe78}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IFNAR1 (interferon alpha and beta receptor subunit 1) [NCBI Gene 3454] {aka AVP, CRF2-1, IFN-R-1, IFN-alpha-REC, IFNAR, IFNBR}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, Bcl2 (B cell leukemia/lymphoma 2) [NCBI Gene 12043] {aka Bcl-2, C430015F12Rik, D630044D05Rik, D830018M01Rik}, Ifnar1 (interferon (alpha and beta) receptor 1) [NCBI Gene 15975] {aka Ifar, Ifnar, Ifrc, Infar}, DGAT2L6 (diacylglycerol O-acyltransferase 2 like 6) [NCBI Gene 347516] {aka DC3}, RIGI (RNA sensor RIG-I) [NCBI Gene 23586] {aka DDX58, RIG-I, RIG1, RLR-1, SGMRT2}, STAT6 (signal transducer and activator of transcription 6) [NCBI Gene 6778] {aka D12S1644, HIES6, IL-4-STAT, STAT6B, STAT6C}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, Nectin1 (nectin cell adhesion molecule 1) [NCBI Gene 58235] {aka Cd111, HIgR, HveC, PRR, PRR1, Pvrl1}, SOCS2 (suppressor of cytokine signaling 2) [NCBI Gene 8835] {aka CIS2, Cish2, SOCS-2, SSI-2, SSI2, STATI2}, TBK1 (TANK binding kinase 1) [NCBI Gene 29110] {aka AIARV, FTDALS4, IIAE8, NAK, T2K}, MST1 (macrophage stimulating 1) [NCBI Gene 4485] {aka D3F15S2, DNF15S2, HGFL, MSP, NF15S2}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, FPR2 (formyl peptide receptor 2) [NCBI Gene 2358] {aka ALX, ALXR, FMLP-R-II, FMLPX, FPR2A, FPRH1}, CASP7 (caspase 7) [NCBI Gene 840] {aka CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}
- **Diseases:** chronic disease (MESH:D002908), viral infections (MESH:D014777), microphthalmia (MESH:D008850), death (MESH:D003643), Leigh syndrome (MESH:D007888), mitochondrial dysregulation (MESH:D021081), DC (MESH:D054740), sinus and fungal infections (MESH:D009181), mitochondrial encephalopathy (MESH:C538525), BMDC (MESH:D001855), metabolic disorders (MESH:D008659), chronic inflammation (MESH:D007249), pneumonia (MESH:D011014), autoimmunity (MESH:D001327), mitochondrial defects (MESH:C565376), Infections (MESH:D007239), MD (MESH:D028361), immune dysregulation (OMIM:614878), lung tumors (MESH:D008175), infectious (MESH:D003141), sepsis (MESH:D018805), hepatocellular carcinoma (MESH:D006528), cancer (MESH:D009369), genetic disorders (MESH:D030342), SIRS (MESH:D018746)
- **Chemicals:** ROS (MESH:D017382), mevalonate (MESH:D008798), ATP (MESH:D000255), rotenone (MESH:D012402), urea (MESH:D014508), oxygen (MESH:D010100), FPP (MESH:C004808), LPS (MESH:D008070), Poly I:C (MESH:D011070), superoxide (MESH:D013481), lipids (MESH:D008055), fatty acid (MESH:D005227), carbon monoxide (MESH:D002248), rapamycin (MESH:D020123), vitamin D3 (MESH:D002762), prostaglandin E2 (MESH:D015232), amino acid (MESH:D000596), glucose (MESH:D005947), etomoxir (MESH:C054207), NO (MESH:D009569), metformin (MESH:D008687), DHE (-), glutamine (MESH:D005973), Antimycin-A (MESH:D000968), dexamethasone (MESH:D003907), ascorbate (MESH:D001205), lactate (MESH:D019344), omega-3 fatty acids (MESH:D015525), 1alpha,25-dihydroxyvitamin D3 (MESH:D002117), 2-NBDG (MESH:C098340)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Cell lines:** TolDC — Mus musculus (Mouse), Transformed cell line (CVCL_VS59), OT-I T — Homo sapiens (Human), Lung small cell carcinoma, Cancer cell line (CVCL_7018), moDC — Homo sapiens (Human), Childhood T acute lymphoblastic leukemia, Cancer cell line (CVCL_LB92), GEN2.2 — Homo sapiens (Human), Blastic plasmacytoid dendritic cell neoplasm, Cancer cell line (CVCL_5G44)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12859203/full.md

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Source: https://tomesphere.com/paper/PMC12859203