bims-mitrat Biomed News
on Mitochondrial transplantation and transfer
Issue of 2026–04–05
six papers selected by
Gökhan Burçin Kubat, Başkent Üni̇versi̇tesi̇



  1. Trends Mol Med. 2026 Apr 02. pii: S1471-4914(26)00061-4. [Epub ahead of print]
      Satellite glial cells transfer mitochondria to sensory neurons via myosin 10-dependent tunneling nanotubes. Ji et al. show that this transfer is impaired in diabetic neuropathy, causing energy failure. Restoring it via cell or mitochondrial transplantation alleviates pain and promotes nerve regeneration, revealing a new therapeutic strategy for peripheral neuropathy.
    Keywords:  diabetic peripheral neuropathy; mitochondrial transfer; neuroprotection; satellite glial cells; tunneling nanotubes
    DOI:  https://doi.org/10.1016/j.molmed.2026.03.004
  2. Cell Commun Signal. 2026 Mar 28.
      
    Keywords:  Extracellular Vesicles; Intercellular Communication; Mitochondrial Transfer; Tumor Microenvironment; Tunneling Nanotubes
    DOI:  https://doi.org/10.1186/s12964-026-02820-4
  3. Front Immunol. 2026 ;17 1698136
       Introduction: Mitochondrial dysfunction has been increasingly implicated in the pathogenesis of multiple sclerosis (MS), contributing to oxidative stress, immune dysregulation, and neurodegeneration. Current therapies primarily target inflammation but do not adequately address mitochondrial impairment or progressive tissue damage. This study aimed to evaluate the therapeutic potential of mitochondrial transplantation in experimental autoimmune encephalomyelitis (EAE), a murine model of MS, by investigating its effects on immune modulation, mitochondrial function, and tissue integrity.
    Methods: EAE was induced in mice using myelin oligodendrocyte glycoprotein. Isolated mitochondria were administered intravenously, and clinical progression, spinal cord histology, immune cell populations, mitochondrial activity, fibrosis, and gut microbiota composition were assessed. Additionally, human peripheral blood mononuclear cells (PBMCs) from MS patients were co-cultured with mitochondria to examine ATP production, reactive oxygen species levels, and T cell differentiation.
    Results: Mitochondrial transplantation significantly reduced EAE severity, spinal cord inflammation, demyelination, and fibrosis. Treated mice showed increased regulatory T (Treg) cells, reduced T helper 17 (Th17) cells, improved mitochondrial biogenesis, and decreased oxidative stress. Gut microbiome analysis revealed beneficial compositional changes. In human PBMCs, mitochondrial transfer enhanced ATP synthesis, suppressed mitochondrial ROS, and promoted Treg differentiation while inhibiting pro-inflammatory cytokines.
    Discussion: Our findings suggest that mitochondrial transplantation restores mitochondrial function, rebalances immune responses, and mitigates neuroinflammation and fibrosis in EAE. This approach offers a novel therapeutic strategy for MS by addressing both metabolic and immunological drivers of disease progression.
    Keywords:  T cell; experimental autoimmune encephalomyelitis (EAE); mitochondria; multiple sclerosis; spinal cord
    DOI:  https://doi.org/10.3389/fimmu.2026.1698136
  4. J Adv Res. 2026 Mar 27. pii: S2090-1232(26)00269-9. [Epub ahead of print]
       BACKGROUND: The homeostatic balance of the immune microenvironment is key to maintaining bodily health, and its disorder is closely related to the occurrence and development of various major diseases such as cardiovascular diseases, autoimmune diseases, tumors, and aging. In recent years, mitochondria have gradually become a research hotspot, breaking the traditional perception of mitochondria solely as the cell's energy factory. Mitochondria precisely regulate the polarization, activation, proliferation, and functional fate of various immune cells through various means such as metabolic reprogramming, dynamics remodeling, autophagy regulation, and intercellular communication. Under pathological conditions, metabolic reprogramming abnormalities, abnormal release of mitochondrial damage-associated molecular patterns (mtDAMPs), and intercellular mitochondrial transfer (IMT) dysfunction can drive pathological remodeling of the immune microenvironment.
    AIM OF REVIEW: This article provides a systematic review centered on the interaction between mitochondria and the immune microenvironment, comprehensively elaborating on aspects such as the regulatory patterns of mitochondria in immune cells, intercellular mitochondrial communication mechanisms, mitochondrial-immune remodeling pathological mechanisms in diseases, novel analytical technologies, and targeted therapeutic strategies. It analyzes the translational feasibility and challenges of mitochondria-targeted therapies, aiming to offer theoretical support and clinical reference for a deeper understanding of the immune regulatory functions of mitochondria and the development of new immunotherapeutic strategies.
    KEY SCIENTIFIC CONCEPTS OF REVIEW: The review highlights that immune cell function relies on cell-type-specific mitochondrial metabolism, alongside the balance of mitochondrial dynamics and mitophagy. Furthermore, IMT and extracellular vesicle (EV)-mediated mtDAMPs signaling form a crucial intercellular communication network that regulates the energy metabolism and immune phenotype of recipient cells. Across various diseases, mitochondrial-immune remodeling points to three conserved checkpoints, providing universal therapeutic targets. Driven by breakthroughs in single-cell sequencing and multi-omics analysis, the decoding of mitochondrial heterogeneity has facilitated a paradigm shift from reactive to predictive and proactive medicine. Finally, this review integrates extensive studies on mitochondria-targeted therapeutic strategies, providing highly translatable avenues for personalized immunotherapy.
    Keywords:  Immune microenvironment; Individualized immunotherapy; Intercellular mitochondrial transfer; Mitochondrial dynamics; Mitochondrial metabolism
    DOI:  https://doi.org/10.1016/j.jare.2026.03.048
  5. J Integr Neurosci. 2026 Mar 25. 25(3): 48953
       BACKGROUND: Cerebral ischemia-reperfusion injury (CIRI) is a severe neurological condition where restoring neuronal mitochondrial function critically impacts prognosis. While electroacupuncture (EA) has demonstrated neuroprotective effects by improving mitochondrial function, the precise underlying mechanisms remain unclear. Emerging evidence suggests that astrocyte-to-neuron mitochondrial transfer, facilitated by mitochondrial Rho-GTPase 1 (Miro1), serves as a vital neuroprotective pathway. Therefore, this study investigates whether astrocytic Miro1 participates in the neuroprotective effects of EA against CIRI in mice by regulating the expression of the mitochondrial marker translocase of the outer mitochondrial membrane 40 (TOM40) and adenosine triphosphate (ATP) levels in damaged neurons.
    METHODS: 126 C57BL/6 mice were randomly allocated into seven experimental groups (n = 18 per group): Sham-operated (Sham), middle cerebral artery occlusion (MCAO) model, EA, sham electroacupuncture (SEA), EA combined with astrocyte-specific Miro1 knockdown (GFAP: glial fibrillary acidic protein, EA+AAV-GFAP-shMiro1), astrocyte-specific Miro1 over-expression (AAV-GFAP-hiMiro1), and adenoviral empty vector control (AAV-GFAP-control). The CIRI model was induced using MCAO. Prior to model induction, the EA group received pretreatment with EA at the Baihui (GV20) acupoint. The SEA group underwent identical procedures to the EA group except for electrical stimulation. For the EA+AAV-GFAP-shMiro1, AAV-GFAP-hiMiro1, and AAV-GFAP-control groups, mice received intracerebroventricular injections of AAV-GFAP-shMiro1, AAV-GFAP-hiMiro1, or AAV-GFAP-control, respectively, 48 hours prior to EA treatment, with other procedures matching the EA group. At 24 hours post-reperfusion, neurological deficit scores, cerebral infarct volume, and neuronal survival in the peri-infarct penumbra were assessed. Astrocytes and neurons from the peri-infarct penumbra were isolated to measure ATP levels and expression of the mitochondrial-specific protein TOM40 in neurons, as well as ATP levels, TOM40, and Miro1 protein expression in astrocytes.
    RESULTS: Relative to the Sham group, the MCAO group displayed a significant increase in cerebral infarct volume and neurological deficit scores, accompanied by a marked reduction in neuronal viability, TOM40 expression, and ATP levels (p < 0.01). In contrast to the MCAO and SEA groups, the EA and AAV-GFAP-hiMiro1 groups demonstrated improved neurological scores, reduced infarct volume, enhanced neuronal viability, elevated neuronal ATP levels and TOM40 expression, as well as decreased astrocytic ATP and TOM40 levels, but significantly increased Miro1 expression in astrocytes (p < 0.01). When compared to the EA group, the EA+AAV-GFAP-shMiro1 group exhibited a reversal of all the aforementioned improvements (p < 0.01), while the AAV-GFAP-hiMiro1 group showed no significant changes (p > 0.05).
    CONCLUSIONS: EA exerts neuroprotective effects in MCAO mice by upregulating Miro1 protein expression in astrocytes and upregulating the mitochondrial marker TOM40 alongside ATP levels in neurons. Silencing Miro1 abolished the neuroprotective effects of EA and reduced neuronal TOM40 expression, while Miro1 overexpression increased this mitochondrial marker and mimicked EA-mediated neuroprotection. These findings identify Miro1 as a key effector of EA-induced neuroprotection, although the upstream signaling pathways linking EA to Miro1 upregulation require further investigation.
    Keywords:  GTP phosphohydrolases; brain ischemia; electroacupuncture; mitochondrial transfer; neuroprotection; reperfusion injury
    DOI:  https://doi.org/10.31083/JIN48953
  6. Cancer Lett. 2026 Mar 26. pii: S0304-3835(26)00220-X. [Epub ahead of print]647 218457
      Recent evidence establishes that melanoma cells actively uptake mitochondria from stromal cells; however, the mitochondrial release in a physiological context remains unstudied. Here, we show that melanoma cells release dysfunctional mitochondria into the extracellular space through a predominantly non-vesicular route. Using melanocyte Melan-a and melanoma B16-F1 and B16-F10 cell lines, we observed increased extracellular mitochondrial release in malignant cells. Electron microscopy revealed these mitochondria lacked cristae and were primarily free organelles. Membrane potential analysis confirmed their dysfunctional state. Mitophagy analysis using mtKeima showed that, under oxidative stress, melanoma cells failed to activate canonical mitophagy and instead upregulated mitochondrial release as an alternative MQC mechanism. Western blot analysis revealed a fission-biased mitochondrial network in melanoma cells, with elevated phospho-DRP1/DRP1 ratio, and a tendency to reduce MFN1 and OPA1. Together with PINK1/ATG7 downregulation and BNIP3/NIX upregulation, suggest a secretory mitophagy phenotype. Tumor-derived mitochondria were detected in both the tumor microenvironment and plasma of melanoma-bearing mice, with extracellular mitochondria levels correlating with tumor burden. Plasma from melanoma patients exhibited elevated levels of TOMM20+ mitochondria compared to healthy donors. Transcriptomic analysis of The Cancer Genome Atlas melanoma cohort revealed that high expression of MQC-related genes DRP1 and BNIP3L was associated with worse prognosis. Collectively, our findings uncover a tumor-intrinsic, non-canonical MQC pathway that releases dysfunctional mitochondria. This mechanism establishes a new paradigm of tumor-host systemic communication, wherein circulating tumor-derived mitochondria might actively influence disease progression. These findings open avenues for developing non-invasive biomarkers and therapeutic strategies targeting mitochondrial release.
    Keywords:  Biomarkers; Extracellular mitochondria; Melanoma; Mitochondrial quality control; Secretory mitophagy
    DOI:  https://doi.org/10.1016/j.canlet.2026.218457