Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

Systemic factors as mediators of brain homeostasis, ageing and neurodegeneration

An Author Correction to this article was published on 13 March 2020

This article has been updated

Abstract

A rapidly ageing population and a limited therapeutic toolbox urgently necessitate new approaches to treat neurodegenerative diseases. Brain ageing, the key risk factor for neurodegeneration, involves complex cellular and molecular processes that eventually result in cognitive decline. Although cell-intrinsic defects in neurons and glia may partially explain this decline, cell-extrinsic changes in the systemic environment, mediated by blood, have recently been shown to contribute to brain dysfunction with age. Here, we review the current understanding of how systemic factors mediate brain ageing, how these factors are regulated and how we can translate these findings into therapies for neurodegenerative diseases.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: A framework for understanding the effects of systemic factors on the brain.
Fig. 2: Effects of cytokines and chemokines on age-related brain dysfunction.

Similar content being viewed by others

Change history

References

  1. Catani, M. & Sandrone, S. Brain Renaissance: From Vesalius to Modern Neuroscience (Oxford Univ. Press, 2015).

  2. Mazzarello, P. A unifying concept: the history of cell theory. Nat. Cell Biol. 1, E13–E15 (1999).

    CAS  PubMed  Google Scholar 

  3. Hill, A. V. Bayliss and Starling and the happy fellowship of physiologists. J. Physiol. 204, 1–13 (1969).

    CAS  PubMed  PubMed Central  Google Scholar 

  4. Junnila, R. K., List, E. O., Berryman, D. E., Murrey, J. W. & Kopchick, J. J. The GH/IGF-1 axis in ageing and longevity. Nat. Rev. Endocrinol. 9, 366–376 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  5. Zárate, S., Stevnsner, T. & Gredilla, R. Role of estrogen and other sex hormones in brain aging. neuroprotection and DNA repair. Front. Aging Neurosci. 9, 430 (2017).

    PubMed  PubMed Central  Google Scholar 

  6. Menni, C. et al. Circulating proteomic signatures of chronological age. J. Gerontol. A Biol. Sci. Med. Sci. 70, 809–816 (2015).

    CAS  PubMed  Google Scholar 

  7. Hu, W. T. et al. Plasma multianalyte profiling in mild cognitive impairment and Alzheimer disease. Neurology 79, 897–905 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  8. Ashton, N. J. et al. A plasma protein classifier for predicting amyloid burden for preclinical Alzheimer’s disease. Sci. Adv. 5, eaau7220 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Tanaka, T. et al. Plasma proteomic signature of age in healthy humans. Aging Cell 17, e12799 (2018).

    PubMed  PubMed Central  Google Scholar 

  10. Sun, B. B. et al. Genomic atlas of the human plasma proteome. Nature 558, 73–79 (2018). Large-scale resource that identified genetic variations associated with plasma protein levels.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Sattlecker, M. et al. Alzheimer’s disease biomarker discovery using SOMAscan multiplexed protein technology. Alzheimers Dement. 10, 724–734 (2014).

    PubMed  Google Scholar 

  12. Eggel, A. & Wyss-Coray, T. A revival of parabiosis in biomedical research. Swiss Med. Wkly. 144, w13914 (2014).

    PubMed  PubMed Central  Google Scholar 

  13. Villeda, S. A. et al. The ageing systemic milieu negatively regulates neurogenesis and cognitive function. Nature 477, 90–94 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Villeda, S. A. et al. Young blood reverses age-related impairments in cognitive function and synaptic plasticity in mice. Nat. Med. 20, 659–663 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Katsimpardi, L. et al. Vascular and neurogenic rejuvenation of the aging mouse brain by young systemic factors. Science 344, 630–634 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Das, M. M. et al. Young bone marrow transplantation preserves learning and memory in old mice. Commun. Biol. 2, 73 (2019).

    PubMed  PubMed Central  Google Scholar 

  17. Smith, L. K. et al. β2-microglobulin is a systemic pro-aging factor that impairs cognitive function and neurogenesis. Nat. Med. 21, 932–937 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  18. Castellano, J. M. et al. Human umbilical cord plasma proteins revitalize hippocampal function in aged mice. Nature 544, 488–492 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  19. Khrimian, L. et al. Gpr158 mediates osteocalcin’s regulation of cognition. J. Exp. Med. 214, 2859–2873 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  20. Gan, K. J. & Südhof, T. C. Specific factors in blood from young but not old mice directly promote synapse formation and NMDA-receptor recruitment. Proc. Natl Acad. Sci. USA 116, 12524–12533 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  21. Sasayama, D. et al. Genome-wide quantitative trait loci mapping of the human cerebrospinal fluid proteome. Hum. Mol. Genet. 26, 44–51 (2017).

    CAS  PubMed  Google Scholar 

  22. Yang, A. C. et al. Multiple click-selective tRNA synthetases expand mammalian cell-specific proteomics. J. Am. Chem. Soc. 140, 7046–7051 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Ngo, J. T., Schuman, E. M. & Tirrell, D. A. Mutant methionyl-tRNA synthetase from bacteria enables site-selective N-terminal labeling of proteins expressed in mammalian cells. Proc. Natl Acad. Sci. USA 110, 4992–4997 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  24. Mahdavi, A. et al. Engineered aminoacyl-tRNA synthetase for cell-selective analysis of mammalian protein synthesis. J. Am. Chem. Soc. 138, 4278–4281 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  25. Elliott, T. S. et al. Proteome labeling and protein identification in specific tissues and at specific developmental stages in an animal. Nat. Biotechnol. 32, 465–472 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  26. Voss, M. W. et al. Exercise and hippocampal memory systems. Trends Cognit. Sci. 23, 318–333 (2019).

    Google Scholar 

  27. Pedersen, B. K. Physical activity and muscle–brain crosstalk. Nat. Rev. Endocrinol. 15, 383–392 (2019).

    PubMed  Google Scholar 

  28. Morland, C. et al. Exercise induces cerebral VEGF and angiogenesis via the lactate receptor HCAR1. Nat. Commun. 8, 15557 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Sherwood, L. M., Parris, E. E. & Cahill, G. F. Jr. Starvation in Man. N. Engl. J. Med. 282, 668–675 (1970).

    Google Scholar 

  30. Sleiman, S. F. et al. Exercise promotes the expression of brain derived neurotrophic factor (BDNF) through the action of the ketone body β-hydroxybutyrate. eLife 5, e15092 (2016).

    PubMed  PubMed Central  Google Scholar 

  31. Alves, S., Fol, R. & Cartier, N. Gene therapy strategies for Alzheimer’s disease: an overview. Hum. Gene Ther. 27, 100–107 (2016).

    CAS  PubMed  Google Scholar 

  32. Didonna, A. & Opal, P. The promise and perils of HDAC inhibitors in neurodegeneration. Ann. Clin. Transl. Neurol. 2, 79–101 (2015).

    CAS  PubMed  Google Scholar 

  33. Moon, H. Y. et al. Running-induced systemic cathepsin B secretion is associated with memory function. Cell Metab. 24, 332–340 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  34. De Miguel, Z. et. al. Exercise conditioned plasma dampens inflammation via clusterin and boosts memory. bioRxiv https://doi.org/10.1101/775288 (2019).

  35. Wrann, C. D. et al. Exercise induces hippocampal BDNF through a PGC-1α/FNDC5 pathway. Cell Metab. 18, 649–659 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  36. Lourenco, M. V. et al. Exercise-linked FNDC5/irisin rescues synaptic plasticity and memory defects in Alzheimer’s models. Nat. Med. 25, 165–175 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  37. Winchester, J. et al. Walking stabilizes cognitive functioning in Alzheimer’s disease (AD) across one year. Arch. Gerontol. Geriatr. 56, 96–103 (2013).

    CAS  PubMed  Google Scholar 

  38. Whitham, M. et al. Extracellular vesicles provide a means for tissue crosstalk during exercise. Cell Metab. 27, 237–251.e4 (2018).

    CAS  PubMed  Google Scholar 

  39. Stefano, G. B. et al. Gut, microbiome, and brain regulatory axis: relevance to neurodegenerative and psychiatric disorders. Cell. Mol. Neurobiol. 38, 1197–1206 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  40. Erny, D. et al. Host microbiota constantly control maturation and function of microglia in the CNS. Nat. Neurosci. 18, 965–977 (2015). First study showing the drastic effects of gut microbiota on microglial maturation.

    CAS  PubMed  PubMed Central  Google Scholar 

  41. Thion, M. S. et al. Microbiome influences prenatal and adult microglia in a sex-specific manner. Cell 172, 500–516.e16 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  42. Sampson, T. R. et al. Gut microbiota regulate motor deficits and neuroinflammation in a model of Parkinson’s disease. Cell 167, 1469–1480.e12 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  43. Harach, T. et al. Reduction of Abeta amyloid pathology in APPPS1 transgenic mice in the absence of gut microbiota. Sci. Rep. 7, 41802 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  44. Minter, M. R. et al. Antibiotic-induced perturbations in microbial diversity during post-natal development alters amyloid pathology in an aged APPSWE/PS1DeltaE9 murine model of Alzheimer’s disease. Sci. Rep. 7, 10411 (2017).

    PubMed  PubMed Central  Google Scholar 

  45. Heneka, M. T., McManus, R. M. & Latz, E. Inflammasome signalling in brain function and neurodegenerative disease. Nat. Rev. Neurosci. 19, 610–621 (2018).

    CAS  PubMed  Google Scholar 

  46. Derecki, N. C. et al. Regulation of learning and memory by meningeal immunity: a key role for IL-4. J. Exp. Med. 207, 1067–1080 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  47. Xu, Y. et al. Unexpected role of interferon-γ in regulating neuronal connectivity and social behaviour. Nature 535, 425–429 (2016).

    PubMed  PubMed Central  Google Scholar 

  48. Dulken, B. W. et al. Single-cell analysis reveals T cell infiltration in old neurogenic niches. Nature 571, 205–210 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  49. Ito, M. et al. Brain regulatory T cells suppress astrogliosis and potentiate neurological recovery. Nature 565, 246–250 (2019).

    CAS  PubMed  Google Scholar 

  50. Derecki, N. C., Quinnies, K. M. & Kipnis, J. Alternatively activated myeloid (M2) cells enhance cognitive function in immune compromised mice. Brain Behav. Immun. 25, 379–385 (2011).

    CAS  PubMed  Google Scholar 

  51. Ruckh, J. M. et al. Rejuvenation of regeneration in the aging central nervous system. Cell Stem Cell 10, 96–103 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  52. Zenaro, E. et al. Neutrophils promote Alzheimer’s disease-like pathology and cognitive decline via LFA-1 integrin. Nat. Med. 21, 880–886 (2015).

    CAS  PubMed  Google Scholar 

  53. Hernandez, J. C. et al. Neutrophil adhesion in brain capillaries reduces cortical blood flow and impairs memory function in Alzheimer’s disease mouse models. Nat. Neurosci. 22, 413–420 (2019).

    Google Scholar 

  54. Ruitenberg, A. et al. Cerebral hypoperfusion and clinical onset of dementia: the Rotterdam study. Ann. Neurol. 57, 789–794 (2005).

    PubMed  Google Scholar 

  55. Montagne, A. et al. Blood–brain barrier breakdown in the aging human hippocampus. Neuron 85, 296–302 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  56. Nation, D. A. et al. Blood–brain barrier breakdown is an early biomarker of human cognitive dysfunction. Nat. Med. 25, 270–276 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  57. Nortley, R. et al. Amyloid β oligomers constrict human capillaries in Alzheimer’s disease via signaling to pericytes. Science 365, eaav9518 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  58. Bell, R. D. et al. Pericytes control key neurovascular functions and neuronal phenotype in the adult brain and during brain aging. Neuron 68, 409–427 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  59. Montagne, A. et al. Pericyte degeneration causes white matter dysfunction in the mouse central nervous system. Nat. Med. 24, 326–337 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  60. Ryu, J. K. et al. Blood coagulation protein fibrinogen promotes autoimmunity and demyelination via chemokine release and antigen presentation. Nat. Commun. 6, 8164 (2015).

    PubMed  Google Scholar 

  61. Ryu, J. K. et al. Fibrin-targeting immunotherapy protects against neuroinflammation and neurodegeneration. Nat. Immunol. 19, 1212–1223 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  62. Merlini, M. et al. Fibrinogen induces microglia-mediated spine elimination and cognitive impairment in an Alzheimer’s disease model. Neuron 101, 1099–1108.e6 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  63. Duan, L. et al. PDGFRβ cells rapidly relay inflammatory signal from the circulatory system to neurons via chemokine CCL2. Neuron 100, 183–200.e8 (2018).

    CAS  PubMed  Google Scholar 

  64. Baruch, K. et al. Aging. Aging-induced type I interferon response at the choroid plexus negatively affects brain function. Science 346, 89–93 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  65. Zhu, L. et al. Klotho controls the brain–immune system interface in the choroid plexus. Proc. Natl Acad. Sci. USA 115, E11388–E11396 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  66. Silva-Vargas, V., Maldonado-Soto, A. R., Mizrak, D., Codega, P. & Doetsch, F. Age-dependent niche signals from the choroid plexus regulate adult neural stem cells. Cell Stem Cell. 19, 643–652 (2016).

    CAS  PubMed  Google Scholar 

  67. Baruch, K. et al. CNS-specific immunity at the choroid plexus shifts toward destructive Th2 inflammation in brain aging. Proc. Natl Acad. Sci. USA 110, 2264 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  68. Baruch, K. et al. Breaking immune tolerance by targeting Foxp3+ regulatory T cells mitigates Alzheimer’s disease pathology. Nat. Commun. 6, 7967 (2015).

    CAS  PubMed  Google Scholar 

  69. Baruch, K. et al. PD-1 immune checkpoint blockade reduces pathology and improves memory in mouse models of Alzheimer’s disease. Nat. Med. 22, 135–137 (2016).

    CAS  PubMed  Google Scholar 

  70. Lee, M.-H. et al. Somatic APP gene recombination in Alzheimer’s disease and normal neurons. Nature 563, 639–645 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  71. Cai, R. et al. Panoptic imaging of transparent mice reveals whole-body neuronal projections and skull-meninges connections. Nat. Neurosci. 22, 317–327 (2019).

    CAS  PubMed  Google Scholar 

  72. Herisson, F. et al. Direct vascular channels connect skull bone marrow and the brain surface enabling myeloid cell migration. Nat. Neurosci. 21, 1209–1217 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  73. Yao, H. et al. Leukaemia hijacks a neural mechanism to invade the central nervous system. Nature 560, 55–60 (2018).

    CAS  PubMed  Google Scholar 

  74. Park, M. H. et al. Vascular and neurogenic rejuvenation in aging mice by modulation of ASM. Neuron 100, 167–182.e9 (2018).

    CAS  PubMed  Google Scholar 

  75. Liu, X. et al. Cell-type-specific interleukin 1 receptor 1 signaling in the brain regulates distinct neuroimmune activities. Immunity 50, 317–333.e6 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  76. Blank, T. et al. Brain endothelial- and epithelial-specific interferon receptor chain 1 drives virus-induced sickness behavior and cognitive impairment. Immunity 44, 901–912 (2016).

    CAS  PubMed  Google Scholar 

  77. Vanlandewijck, M. et al. A molecular atlas of cell types and zonation in the brain vasculature. Nature 554, 475–480 (2018).

    CAS  PubMed  Google Scholar 

  78. Sabbagh, M. F. et al. Transcriptional and epigenomic landscapes of CNS and non-CNS vascular endothelial cells. eLife 7, e36187 (2018).

    PubMed  PubMed Central  Google Scholar 

  79. Yousef, H. et al. Aged blood impairs hippocampal neural precursor activity and activates microglia via brain endothelial cell VCAM1. Nat. Med. 25, 988–1000 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  80. Chen, M. B. et al. Brain endothelial cells are exquisite sensors of age-related circulatory cues. bioRxiv. https://doi.org/10.1101/617258 (2019).

    Article  Google Scholar 

  81. Hickman, S. E. et al. The microglial sensome revealed by direct RNA sequencing. Nat. Neurosci. 16, 1896–1905 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  82. Deczkowska, A. et al. Disease-associated microglia: a universal immune sensor of neurodegeneration. Cell 173, 1073–1081 (2018).

    CAS  PubMed  Google Scholar 

  83. Pluvinage, J. V. et al. CD22 blockade restores homeostatic microglial phagocytosis in ageing brains. Nature 568, 187–192 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  84. Marschallinger, J. et al. Lipid droplet accumulating microglia represent a dysfunctional and pro-inflammatory state in the aging brain. bioRxiv https://doi.org/10.1101/722827 (2019).

    Article  Google Scholar 

  85. Bialas, A. R. et al. Microglia-dependent synapse loss in type I interferon-mediated lupus. Nature 546, 539–543 (2017).

    CAS  PubMed  Google Scholar 

  86. Deczkowska, A. et al. Mef2C restrains microglial inflammatory response and is lost in brain ageing in an IFN-I-dependent manner. Nat. Commun. 8, 717 (2017).

    PubMed  PubMed Central  Google Scholar 

  87. Clarke, L. E. et al. Normal aging induces A1-like astrocyte reactivity. Proc. Natl Acad. Sci. USA 115, E1896–E1905 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  88. Boisvert, M. M., Erikson, G. A., Shokhirev, M. N. & Allen, N. J. The aging astrocyte transcriptome from multiple regions of the mouse brain. Cell Rep. 22, 269–285 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  89. Liddelow, S. A. et al. Neurotoxic reactive astrocytes are induced by activated microglia. Nature 541, 481–487 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  90. Banks, W. A., Kastin, A. J. & Broadwell, R. D. Passage of cytokines across the blood–brain barrier. Neuroimmunomodulation 2, 241–248 (1995).

    CAS  PubMed  Google Scholar 

  91. Falcao, A. M. et al. Disease-specific oligodendrocyte lineage cells arise in multiple sclerosis. Nat. Med. 24, 1837–1844 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  92. Spitzer, S. O. et al. Oligodendrocyte progenitor cells become regionally diverse and heterogeneous with age. Neuron 101, 459–471.e5 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  93. Gutierrez, E. G., Banks, W. A. & Kastin, A. J. Murine tumor necrosis factor alpha is transported from blood to brain in the mouse. J. Neuroimmunol. 47, 169–176 (1993).

    CAS  PubMed  Google Scholar 

  94. Stellwagen, D. & Malenka, R. C. Synaptic scaling mediated by glial TNF-α. Nature 440, 1054–1059 (2006).

    CAS  PubMed  Google Scholar 

  95. Prieto, G. A. et al. Synapse-specific IL-1 receptor subunit reconfiguration augments vulnerability to IL-1β in the aged hippocampus. Proc. Natl Acad. Sci. USA 112, E5078–E5087 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  96. Luo, J. et al. Colony-stimulating factor 1 receptor (CSF1R) signaling in injured neurons facilitates protection and survival. J. Exp. Med. 210, 157–172 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  97. Boyd, T. D. et al. GM-CSF upregulated in rheumatoid arthritis reverses cognitive impairment and amyloidosis in Alzheimer mice. J. Alzheimers Dis. 21, 507–518 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  98. Rasmussen, M. K., Mestre, H. & Nedergaard, M. The glymphatic pathway in neurological disorders. Lancet Neurol. 17, 1016–1024 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  99. Da Mesquita, S., Fu, Z. & Kipnis, J. The meningeal lymphatic system: a new player in neurophysiology. Neuron 100, 375–388 (2018).

    PubMed  PubMed Central  Google Scholar 

  100. Iliff, J. J. et al. A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid β. Sci. Transl. Med. 4, 147ra111 (2012).

    PubMed  PubMed Central  Google Scholar 

  101. Iliff, J. J. et al. Cerebral arterial pulsation drives par- avascular CSF-interstitial fluid exchange in the murine brain. J. Neurosci. 33, 18190–18199 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  102. Kress, B. T. et al. Impairment of paravascular clearance pathways in the aging brain. Ann. Neurol. 76, 845–861 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  103. Holth, J. K. et al. The sleep-wake cycle regulates brain interstitial fluid tau in mice and CSF tau in humans. Science 363, 880–884 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  104. Hsu, M. et al. Neuroinflammation-induced lymphangiogenesis near the cribriform plate contributes to drainage of CNS-derived antigens and immune cells. Nat. Commun. 10, 229 (2019).

    PubMed  PubMed Central  Google Scholar 

  105. Louveau, A. et al. Structural and functional features of central nervous system lymphatic vessels. Nature 523, 337–341 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  106. Da Mesquita, S. et al. Functional aspects of meningeal lymphatics in ageing and Alzheimer’s disease. Nature 560, 185–191 (2018).

    PubMed  PubMed Central  Google Scholar 

  107. Ahn, J. H. et al. Meningeal lymphatic vessels at the skull base drain cerebrospinal fluid. Nature 572, 62–66 (2019).

    CAS  PubMed  Google Scholar 

  108. Lehallier, B. et al. Undulating changes in human plasma proteome across lifespan are linked to disease. Nat. Med. 25, 1843–1850 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  109. Emilsson, V. et al. Co-regulatory networks of human serum proteins link genetics to disease. Science 361, 769–773 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  110. Swaminathan, J. et al. Highly parallel single-molecule identification of proteins in zeptomole-scale mixtures. Nat. Biotechnol. 36, 1076–1082 (2018).

    CAS  Google Scholar 

  111. Ben-Shaanan, T. L. et al. Activation of the reward system boosts innate and adaptive immunity. Nat. Med. 22, 940–944 (2016).

    CAS  PubMed  Google Scholar 

  112. Middeldorp, J. et al. Preclinical assessment of young blood plasma for Alzheimer disease. JAMA Neurol. 73, 1325–1333 (2016).

    PubMed  PubMed Central  Google Scholar 

  113. Sha, S. J. et al. Safety, tolerability, and feasibility of young plasma infusion in the plasma for Alzheimer symptom Amelioration study: a randomized clinical trial. JAMA Neurol. 76, 35–40 (2019).

    PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by a National Institutes of Health National Institute on Ageing (NIA) grant F30 AG055255 (J.P.), DP1 AG060638 (T.W.-C.), and the NOMIS Foundation (T.W.-C.).

Author information

Authors and Affiliations

Authors

Contributions

Both authors contributed equally to all aspects of the manuscript.

Corresponding authors

Correspondence to John V. Pluvinage or Tony Wyss-Coray.

Ethics declarations

Competing interests

T.W.-C. is a co-founder, shareholder and paid consultant of Alkahest, Inc., a company that develops treatments for CNS diseases based on the concept that circulatory factors regulate brain function. J.V.P. declares no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Glossary

Parabionts

Animals that share partial blood circulation with another animal via surgical anastomosis.

Type 2 T helper cell phenotype

CD4+ T cells that produce high levels of IL-4, IL-5 and IL-13, but little or no IFNγ, IL-2 or TNF. Canonically, these cells protect against multicellular parasites.

Caveolae-mediated transcytosis

A form of clathrin-independent endocytosis that facilitates non-specific transcytosis of extracellular molecules across the BBB, which are then trafficked across the cell in pH-neutral compartments called caveosomes.

Aptamer-based proteomics

A technique that uses short single-stranded oligonucleotides called aptamers to bind and identify proteins in a complex mixture with high affinity and specificity.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pluvinage, J.V., Wyss-Coray, T. Systemic factors as mediators of brain homeostasis, ageing and neurodegeneration. Nat Rev Neurosci 21, 93–102 (2020). https://doi.org/10.1038/s41583-019-0255-9

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41583-019-0255-9

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing