# Periodic Therapeutic Phlebotomy Mitigates Systemic Aging Phenotypes by Promoting Bone Marrow Function

**Authors:** Ji‐Ru Cai, Jian Zhang, Yue‐Xin Ning, Jing Zhang, Tian‐Ce Xu, Mei‐Chen Liu, Ke‐Xin Wang, Hui‐Sheng Chen

PMC · DOI: 10.1111/acel.70400 · Aging Cell · 2026-02-02

## TL;DR

Periodic blood removal in aging models improves health by restoring bone marrow function and reducing aging signs.

## Contribution

Periodic therapeutic phlebotomy is shown to mitigate systemic aging through bone marrow restoration.

## Key findings

- Periodic phlebotomy reduces aging-related behavioral deficits and neurogenesis decline.
- Phlebotomy decreases senescence-associated secretory phenotype levels and tissue degradation.
- Bone marrow restoration via phlebotomy rebalances hematopoiesis and peripheral blood function.

## Abstract

Aging is the primary risk factor for numerous chronic diseases, making the identification of safe and effective anti‐aging strategies a critical focus in biomedical research. Heterochronic parabiosis by blood exchange shows that the exchange interaction between young and old plasma can exert anti‐aging effects through exchange of bloodborne factors. However, the limited plasma source greatly affects clinical translation. Here, we demonstrate that periodic therapeutic phlebotomy in D‐galactose‐induced aging models exerts significant and comprehensive anti‐aging effects, which is reflected by a notable improvement in aging‐associated behavioral deficits and neurogenesis, a significant decrease in the level of circulating senescence‐associated secretory phenotypes, and an obvious mitigation of aging‐associated structural degradation and molecular alterations within the muscle, bone, liver, kidney, and nervous systems. Mechanistically, periodic therapeutic phlebotomy induces bone marrow microenvironment restoration through functional rescue of mesenchymal stem cells and endothelial cells, thereby reestablishing balanced hematopoietic homeostasis. This hematopoietic revitalization subsequently drives systemic improvements in peripheral blood composition and function. In conclusion, our work provides preliminary evidence suggesting that periodic therapeutic phlebotomy exerts anti‐aging effects by restoring bone marrow function and mitigating aging phenotypes, subsequently driving peripheral blood functional restoration. Given its technical simplicity and safety profile, this periodic therapeutic phlebotomy strategy will hold potential to pave the way for clinical translation.

In D‐galactose‐induced aging model, periodic therapeutic phlebotomy exerts significant and comprehensive anti‐aging effects by inducing bone marrow microenvironment restoration, which rebalances hematopoiesis to restore peripheral blood function and ameliorate systemic aging phenotypes. This finding provides preliminary evidence suggesting anti‐aging effects of periodic therapeutic phlebotomy.

## Linked entities

- **Chemicals:** D-galactose (PubChem CID 206)

## Full-text entities

- **Genes:** Cdkn2a (cyclin-dependent kinase inhibitor 2A) [NCBI Gene 25163] {aka Arf, INK4A, MTS1, p16, p16Cdkn2a, p19ARF}, Kl (Klotho) [NCBI Gene 83504], Glb1 (galactosidase, beta 1) [NCBI Gene 316033], Ptpn1 (protein tyrosine phosphatase, non-receptor type 1) [NCBI Gene 24697] {aka Ptp, Ptp1b}, Thy1 (Thy-1 cell surface antigen) [NCBI Gene 24832] {aka CD7}, Dcx (doublecortin) [NCBI Gene 84394], Sirt2 (sirtuin 2) [NCBI Gene 361532], Ccl5 (C-C motif chemokine ligand 5) [NCBI Gene 81780] {aka Rantes, Scya5}, Mpp1 (MAGUK p55 scaffold protein 1) [NCBI Gene 652956] {aka p55}, Hmgb1 (high mobility group box 1) [NCBI Gene 25459] {aka Ac2-008, Hmg1}, Igf1 (insulin-like growth factor 1) [NCBI Gene 24482] {aka IGF}, Anxa5 (annexin A5) [NCBI Gene 25673] {aka Anx5, CPB-I, LC5}, Mapt (microtubule-associated protein tau) [NCBI Gene 29477] {aka MAPT_0N4R, MAPT_1N4R, MAPT_2N4R, Mtapt, RNPTAU, Tau}, Cd48 (Cd48 molecule) [NCBI Gene 245962] {aka SLAMF2}, Cd34 (CD34 molecule) [NCBI Gene 305081], Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Cotl1 (coactosin-like F-actin binding protein 1) [NCBI Gene 361422] {aka Clp}, Glb1 (galactosidase, beta 1) [NCBI Gene 12091] {aka Bge, Bgl, Bgl-e, Bgl-s, Bgl-t, Bgs}, Ascl1 (achaete-scute family bHLH transcription factor 1) [NCBI Gene 64186] {aka Mash1}, Ptpru (protein tyrosine phosphatase receptor type U) [NCBI Gene 19273] {aka Ftp-1, PCP-2, PTP, PTP-lambda, PTPlambda, Pcp2}, Tpo (thyroid peroxidase) [NCBI Gene 54314], Acsl1 (acyl-CoA synthetase long-chain family member 1) [NCBI Gene 25288] {aka ACS, Acas, COAA, Facl2}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 59086] {aka Tgfb}, Il1a (interleukin 1 alpha) [NCBI Gene 24493] {aka IL-1 alpha, IL-1F1}, Psen1 (presenilin 1) [NCBI Gene 19164] {aka Ad3h, PS-1, PS1, S182}, Itgam (integrin subunit alpha M) [NCBI Gene 25021] {aka Cd11b}, Kras (KRAS proto-oncogene, GTPase) [NCBI Gene 24525] {aka K-ras, Kras2, c-Ki-ras, p21}, Mpp4 (MAGUK p55 scaffold protein 4) [NCBI Gene 58808] {aka Dlg6}, Pals1 (protein associated with LIN7 1, MAGUK p55 family member) [NCBI Gene 314259] {aka Mpp5}, Actb (actin, beta) [NCBI Gene 81822] {aka Actx}, Sox2 (SRY-box transcription factor 2) [NCBI Gene 499593] {aka RGD1565646}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Gh1 (growth hormone 1) [NCBI Gene 24391] {aka Gh, Ghb1, RNGHGP}, Syp (synaptophysin) [NCBI Gene 20977] {aka A230093K24Rik, Syn, p38}, Nt5e (5' nucleotidase, ecto) [NCBI Gene 58813] {aka CD73, Nt5}, Slc27a5 (solute carrier family 27 member 5) [NCBI Gene 79111] {aka BAL, rBAL-1}, Rnase1 (ribonuclease A family member 1, pancreatic) [NCBI Gene 364304] {aka RL1, Rib1}, Cd3e (CD3 epsilon subunit of T-cell receptor complex) [NCBI Gene 315609], Cdkn1b (cyclin-dependent kinase inhibitor 1B) [NCBI Gene 83571] {aka CDKN4, Cdki1b, Kip1, P27KIP1, p27}, Nefl (neurofilament light chain) [NCBI Gene 83613] {aka NF-L, NF68, Nfl}, Kit (KIT proto-oncogene receptor tyrosine kinase) [NCBI Gene 64030], Tpo (thyroid peroxidase) [NCBI Gene 22018], Mpp2 (MAGUK p55 scaffold protein 2) [NCBI Gene 85275] {aka Dlg2}, Ptprc (protein tyrosine phosphatase, receptor type, C) [NCBI Gene 24699] {aka CD45, L-CA, Lca, RT7, T200}, Grin2b (glutamate receptor, ionotropic, NMDA2B (epsilon 2)) [NCBI Gene 14812] {aka GluN2B, GluRepsilon2, NR2B, Nmdar2b}, Gpx1 (glutathione peroxidase 1) [NCBI Gene 24404] {aka GSHPx, GSHPx-1}, Cdkn1a (cyclin-dependent kinase inhibitor 1A) [NCBI Gene 114851] {aka Cip1, UV96, Waf1}, Des (desmin) [NCBI Gene 64362], Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, Dlg4 (discs large MAGUK scaffold protein 4) [NCBI Gene 13385] {aka Dlgh4, PSD-95, PSD95, SAP90, SAP90A}, Mpp3 (MAGUK p55 scaffold protein 3) [NCBI Gene 114202] {aka CSG18, Dlg3, Dusp3}, p53-ps (Wistar clone pR53P1 p53 pseudogene) [NCBI Gene 301300], Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, Cdkn2b (cyclin-dependent kinase inhibitor 2B) [NCBI Gene 25164] {aka p15}, Gfap (glial fibrillary acidic protein) [NCBI Gene 24387]
- **Diseases:** neurodegenerative diseases (MESH:D019636), anemia (MESH:D000740), vascular dysfunction (MESH:D002561), blood loss (MESH:D016063), hepatic lipidosis (MESH:D008064), Ischemic (MESH:D002545), hemorrhage (MESH:D006470), asphyxiation (MESH:C537571), fibrosis (MESH:D005355), neuronal degeneration (MESH:D009410), cancers (MESH:D009369), hypoxic (MESH:D002534), Cognitive alterations (MESH:D003072), cardiovascular diseases (MESH:D002318), depression (MESH:D003866), Alzheimer's disease (MESH:D000544), chronic inflammation (MESH:D007249), shock (MESH:D012769), renal damage (MESH:D007674), anxiety (MESH:D001007), impaired osteogenesis (MESH:D010013), behavioral deficits (MESH:D019958), deterioration in learning and memory functions (MESH:D007859)
- **Chemicals:** pyruvate (MESH:D019289), DAPI (MESH:C007293), D-glucose (MESH:D005947), TRIzol (MESH:C411644), Alexa Fluor 488 (MESH:C000711379), K2CrO4 (MESH:C027373), lipid (MESH:D008055), SDS (MESH:D012967), NO (MESH:D009614), formaldehyde (MESH:D005557), nitrogen (MESH:D009584), iron (MESH:D007501), D-gal (MESH:D005690), HgCl2 (MESH:D008627), citrate (MESH:D019343), ammonia (MESH:D000641), 4-AP (MESH:D015761), dimethylformamide (MESH:D004126), HE (-), MgCl2 (MESH:D015636), creatinine (MESH:D003404), Eosin (MESH:D004801), TBIL (MESH:D001663), O2 (MESH:D010100), sodium thiosulfate (MESH:C017717), Taurine (MESH:D013654), 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide (MESH:C022616), TTX (MESH:D013779), EGTA (MESH:D004533), sucrose (MESH:D013395), Tween-20 (MESH:D011136), CaCl2 (MESH:D002122), ethanol (MESH:D000431), PI (MESH:D011419), EDTA (MESH:D004492), NaHCO3 (MESH:D017693), HEPES (MESH:D006531), MDA (MESH:D008315), DAF-2DA (MESH:C414689), KCl (MESH:D011189), water (MESH:D014867), hydrogen peroxide (MESH:D006861), NaCl (MESH:D012965), isoflurane (MESH:D007530), MTT (MESH:C070243), CO2 (MESH:D002245), paraffin (MESH:D010232), Oil Red O (MESH:C011049), picrotoxin (MESH:D010852), K2Cr2O7 (MESH:D011192), Hematoxylin (MESH:D006416)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12862434/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12862434/full.md

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Source: https://tomesphere.com/paper/PMC12862434