Microglia: Rheostats of space radiation effects in the CNS microenvironment
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Microglia are innate immune cells within the brain that arise from a distinct myeloid lineage. Like other tissue resident macrophages, microglia respond to injury or immune challenges and participate in reparative processes such as phagocytosis to preserve normal function. Importantly, they also participate in normal homeostatic processes including maintenance of neurogenic niches and synaptic plasticity associated with development. This review highlights aspects of microglial biology and how repeated insults that occur with age, neurodegenerative disease and possibly radiation exposure may heighten microglial responses and contribute to their dysfunction, creating a situation where their normal reparative mechanisms are no longer sufficient to maintain brain health. These ideas are discussed in the context of an evolving literature focused on microglial responses as possible targets for mitigation of late CNS radiation effects that represent potential risks for future exploration of deep space environments.
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Approaches targeting microglia and associated inflammatory signaling pathways may provide avenues for prevention or mitigation of CNS-specific radiation effects.
“Approaches targeting microglia and associated inflammatory signaling pathways may provide avenues for prevention or mitigation of CNS-specific radiation effects (O'Banion, 2022).”
From Breaking the limit: Biological countermeasures for space radiation exposure to enable long-duration spaceflight (2022) · cites this paper as O'Banion, 2022
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Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner
Schafer, D. P., Lehrman, E. K., Kautzman, A. G., Koyama, R., Mardinly, A. R., Yamasaki, R., Ransohoff, R. M., Greenberg, M. E., Barres, B. A., & Stevens, B. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.026 · Cited by 4,089 · see citing works
Complement and microglia mediate early synapse loss in Alzheimer mouse models
Hong, S., Beja-Glasser, V. F., Nfonoyim, B. M., Frouin, A., Li, S., Ramakrishnan, S., Merry, K. M., Shi, Q., Rosenthal, A., Barres, B. A., et al. (2016) · Science · doi:10.1126/science.aad8373 · Cited by 3,343 · see citing works
Disease-Associated Microglia: A Universal Immune Sensor of Neurodegeneration
Deczkowska, A., Keren-Shaul, H., Weiner, A., Colonna, M., Schwartz, M., & Amit, I. (2018) · Cell · doi:10.1016/j.cell.2018.05.003 · Cited by 1,474 · see citing works
Clearance of senescent glial cells prevents tau-dependent pathology and cognitive decline
Bussian, T. J., Aziz, A., Meyer, C. F., Swenson, B. L., van Deursen, J. M., & Baker, D. J. (2018) · Nature · doi:10.1038/s41586-018-0543-y · Cited by 1,289 · see citing works
Innate immune memory in the brain shapes neurological disease hallmarks
Wendeln, A.-C., Degenhardt, K., Kaurani, L., Gertig, M., Ulas, T., Jain, G., Wagner, J., Häsler, L. M., Wild, K., Skodras, A., et al. (2018) · Nature · doi:10.1038/s41586-018-0023-4 · Cited by 956 · see citing works
A Network of Macrophages Supports Mitochondrial Homeostasis in the Heart
Nicolás-Ávila, J. A., Lechuga-Vieco, A. V., Esteban-Martínez, L., Sánchez-Díaz, M., Díaz-García, E., Santiago, D. J., Rubio-Ponce, A., Li, J. L., Balachander, A., Quintana, J. A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.031 · Cited by 762 · see citing works
Microglia: Dynamic Mediators of Synapse Development and Plasticity
Wu, Y., Dissing-Olesen, L., MacVicar, B. A., & Stevens, B. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.08.008 · Cited by 661 · see citing works
Complement C3 deficiency protects against neurodegeneration in aged plaque-rich APP/PS1 mice
Shi, Q., Chowdhury, S., Ma, R., Le, K. X., Hong, S., Caldarone, B. J., Stevens, B., & Lemere, C. A. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf6295 · Cited by 593 · see citing works
Huang, Y., Xu, Z., Xiong, S., Sun, F., Qin, G., Hu, G., Wang, J., Zhao, L., Liang, Y.-X., Wu, T., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0090-8 · Cited by 560 · see citing works
Immunology of aging: the birth of inflammaging
Fulop, T., Larbi, A., Pawelec, G., Khalil, A., Cohen, A. A., Hirokawa, K., Witkowski, J. M., & Franceschi, C. (2021) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-021-08899-6 · Cited by 464 · see citing works
Norden, D. M., Muccigrosso, M. M., & Godbout, J. P. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.028 · Cited by 413 · see citing works
Ogrodnik, M., Evans, S. A., Fielder, E., Victorelli, S., Kruger, P., Salmonowicz, H., Weigand, B. M., Patel, A. D., Pirtskhalava, T., Inman, C. L., et al. (2021) · Aging Cell · doi:10.1111/acel.13296 · Cited by 405 · see citing works
Complement<i>C3</i>-Deficient Mice Fail to Display Age-Related Hippocampal Decline
Shi, Q., Colodner, K. J., Matousek, S. B., Merry, K., Hong, S., Kenison, J. E., Frost, J. L., Le, K. X., Li, S., Dodart, J.-C., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1698-15.2015 · Cited by 368 · see citing works
Astrocyte senescence: Evidence and significance
Cohen, J., & Torres, C. (2019) · Aging Cell · doi:10.1111/acel.12937 · Cited by 281 · see citing works
Beyond Activation: Characterizing Microglial Functional Phenotypes
Lier, J., Streit, W. J., & Bechmann, I. (2021) · Cells · doi:10.3390/cells10092236 · Cited by 274 · see citing works
Simonsen, L. C., Slaba, T. C., Guida, P., & Rusek, A. (2020) · PLOS Biology · doi:10.1371/journal.pbio.3000669 · Cited by 267 · see citing works
Elimination of microglia improves cognitive function following cranial irradiation
Acharya, M. M., Green, K. N., Allen, B. D., Najafi, A. R., Syage, A., Minasyan, H., Le, M. T., Kawashita, T., Giedzinski, E., Parihar, V. K., et al. (2016) · Scientific Reports · doi:10.1038/srep31545 · Cited by 259 · see citing works
How microglia sense and regulate neuronal activity
Umpierre, A. D., & Wu, L. (2021) · Glia · doi:10.1002/glia.23961 · Cited by 237 · see citing works
Cosmic radiation exposure and persistent cognitive dysfunction
Parihar, V. K., Allen, B. D., Caressi, C., Kwok, S., Chu, E., Tran, K. K., Chmielewski, N. N., Giedzinski, E., Acharya, M. M., Britten, R. A., et al. (2016) · Scientific Reports · doi:10.1038/srep34774 · Cited by 221 · see citing works
What happens to your brain on the way to Mars
Parihar, V. K., Allen, B., Tran, K. K., Macaraeg, T. G., Chu, E. M., Kwok, S. F., Chmielewski, N. N., Craver, B. M., Baulch, J. E., Acharya, M. M., et al. (2015) · Science Advances · doi:10.1126/sciadv.1400256 · Cited by 217 · see citing works
Astrocyte senescence promotes glutamate toxicity in cortical neurons
Limbad, C., Oron, T. R., Alimirah, F., Davalos, A. R., Tracy, T. E., Gan, L., Desprez, P.-Y., & Campisi, J. (2020) · PLOS ONE · doi:10.1371/journal.pone.0227887 · Cited by 183 · see citing works
Parihar, V. K., Maroso, M., Syage, A., Allen, B. D., Angulo, M. C., Soltesz, I., & Limoli, C. L. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.03.009 · Cited by 127 · see citing works
Raber, J., Yamazaki, J., Torres, E. R. S., Kirchoff, N., Stagaman, K., Sharpton, T., Turker, M. S., & Kronenberg, A. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00179 · Cited by 78 · see citing works
Hinkle, J. J., Olschowka, J. A., Love, T. M., Williams, J. P., & O’Banion, M. K. (2019) · Scientific Reports · doi:10.1038/s41598-019-55366-6 · Cited by 61 · see citing works
Self-citationSishc, B. J., Zawaski, J., Saha, J., Carnell, L. S., Fabre, K. M., & Elgart, S. R. (2022) · Life Sciences in Space Research · doi:10.1016/j.lssr.2022.06.003 · Cited by 23 · see citing works
Rosi, S. (2018) · Brain Circulation · doi:10.4103/bc.bc_24_18 · Cited by 18 · see citing works
Flagged first, then by citations
Research works printed but not linked: 68
- Abels, ER, Nieland, L, Hickman, S, Broekman, MLD, El Khoury, J, Maas, SLN, 2021. Comparative analysis identifies similarities between the human and murine microglial sensomes. Int. J. Mol. Sci. 22 (3) https://doi.org/10.3390/ijms22031495. · DOI
- Allen, BD, Syage, AR, Maroso, M, Baddour, AAD, Luong, V, Minasyan, H, et al., 2020. Mitigation of helium irradiation-induced brain injury by microglia depletion. J. Neuroinflamm. 17 (1), 159. https://doi.org/10.1186/s12974-020-01790-9. · DOI
- Belcher, EK, Sweet, TB, Karaahmet, B, Dionisio-Santos, DA, Owlett, LD, Leffler, KA, et al., 2020. Crainial irradiation acutely and persistently impairs injury-induced microglial proliferation. Brain Behav. Immun. -Health 4, 100057. https://doi.org/10.1016/j. bbih.2020.100057. · DOI
- Betlazar, C, Middleton, RJ, Howell, N, Storer, B, Davis, E, Davies, J, et al., 2021. Mitochondrial Translocator Protein (TSPO) expression in the brain after whole body gamma irradiation. Front. Cell Dev. Biol. 9, 715444 https://doi.org/10.3389/ fcell.2021.715444. · DOI
- Chakraborti, A, Allen, A, Allen, B, Rosi, S, Fike, JR, 2012. Cranial irradiation alters dendritic spine density and morphology in the hippocampus. PLoS One 7 (7), e40844. https://doi.org/10.1371/journal.pone.0040844. · DOI
- Cherry, JD, Olschowka, JA, O'Banion, MK, 2014. Neuroinflammation and M2 microglia: the good, the bad, and the inflamed. J. Neuroinflamm. 11, 98. https://doi.org/ 10.1186/1742-2094-11-98. · DOI · Paper page
- Davalos, D, Grutzendler, J, Yang, G, Kim, JV, Zuo, Y, Jung, S, et al., 2005. ATP mediates rapid microglial response to local brain injury in vivo. Nat. Neurosci. 8 (6), 752-758. https://doi.org/10.1038/nn1472. · DOI · Paper page
- Diaz-Aparicio, I, Paris, I, Sierra-Torre, V, Plaza-Zabala, A, Rodriguez-Iglesias, N, Marquez-Ropero, M, et al., 2020. Microglia actively remodel adult hippocampal neurogenesis through the phagocytosis secretome. J. Neurosci. 40 (7), 1453-1482. https://doi.org/10.1523/JNEUROSCI.0993-19.2019. · DOI · Paper page
- Dickstein, DL, Talty, R, Bresnahan, E, Varghese, M, Perry, B, Janssen, WGM, et al., 2018. Alterations in synaptic density and myelination in response to exposure to high- energy charged particles. J. Comp. Neurol. 526 (17), 2845-2855. https://doi.org/ 10.1002/cne.24530. · DOI
- Dubbelaar, ML, Kracht, L, Eggen, BJL, Boddeke, E., 2018. The kaleidoscope of microglial phenotypes. Front. Immunol. 9, 1753. https://doi.org/10.3389/fimmu.2018.01753. · DOI
- Elmore, MR, Najafi, AR, Koike, MA, Dagher, NN, Spangenberg, EE, Rice, RA, et al., 2014. Colony-stimulating factor 1 receptor signaling is necessary for microglia viability, unmasking a microglia progenitor cell in the adult brain. Neuron 82 (2), 380-397. https://doi.org/10.1016/j.neuron.2014.02.040. · DOI · Paper page
- Feng, X, Jopson, TD, Paladini, MS, Liu, S, West, BL, Gupta, N, et al., 2016. Colony- stimulating factor 1 receptor blockade prevents fractionated whole-brain irradiation- induced memory deficits. J. Neuroinflamm. 13 (1), 215. https://doi.org/10.1186/ s12974-016-0671-y. · DOI
- Franceschi, C, Garagnani, P, Parini, P, Giuliani, C, Santoro, A., 2018. Inflammaging: a new immune-metabolic viewpoint for age-related diseases. Nat. Rev. Endocrinol. 14 (10), 576-590. https://doi.org/10.1038/s41574-018-0059-4. · DOI · Paper page
- Ginhoux, F, Greter, M, Leboeuf, M, Nandi, S, See, P, Gokhan, S, et al., 2010. Fate mapping analysis reveals that adult microglia derive from primitive macrophages. Science 330 (6005), 841-845. https://doi.org/10.1126/science.1194637. · DOI · Paper page
- Ginhoux, F, Prinz, M, 2015. Origin of microglia: current concepts and past controversies. Cold Spring Harb. Perspect. Biol. 7 (8), a020537 https://doi.org/10.1101/ cshperspect.a020537. · DOI · Paper page
- He, S, Sharpless, NE, 2017. Senescence in Health and Disease. Cell 169 (6), 1000-1011. https://doi.org/10.1016/j.cell.2017.05.015. · DOI · Paper page
- Hinkle, JJ, Olschowka, JA, Williams, JP, O'Banion, MK, 2020. Pharmacologic manipulation of complement receptor 3 prevents dendritic spine loss and cognitive impairment after acute cranial radiation. bioRxiv. https://doi.org/10.1101/ 2020.11.25.398701, 2020.11.25.398701. · DOI
- Keren-Shaul, H, Spinrad, A, Weiner, A, Matcovitch-Natan, O, Dvir-Szternfeld, R, Ulland, TK, et al., 2017. A unique microglia type associated with restricting development of Alzheimer's disease. Cell 169 (7), 1276-1290. https://doi.org/ 10.1016/j.cell.2017.05.018 e17. · DOI · Paper page
- Knuesel, I, Chicha, L, Britschgi, M, Schobel, SA, Bodmer, M, Hellings, JA, et al., 2014. Maternal immune activation and abnormal brain development across CNS disorders. Nat. Rev. Neurol. 10 (11), 643-660. https://doi.org/10.1038/nrneurol.2014.187. · DOI · Paper page
- Kreisl, WC, Kim, MJ, Coughlin, JM, Henter, ID, Owen, DR, Innis, RB., 2020. PET imaging of neuroinflammation in neurological disorders. Lancet Neurol. 19 (11), 940-950. https://doi.org/10.1016/S1474-4422(20)30346-X. · DOI
- Krukowski, K, Feng, X, Paladini, MS, Chou, A, Sacramento, K, Grue, K, et al., 2018. Temporary microglia-depletion after cosmic radiation modifies phagocytic activity and prevents cognitive deficits. Sci. Rep. 8 (1), 7857. https://doi.org/10.1038/ s41598-018-26039-7. · DOI · Paper page
- Krukowski, K, Grue, K, Becker, M, Elizarraras, E, Frias, ES, Halvorsen, A, et al., 2021. The impact of deep space radiation on cognitive performance: from biological sex to biomarkers to countermeasures. Sci. Adv. 7 (42), eabg6702. https://doi.org/ 10.1126/sciadv.abg6702. · DOI
- Krukowski, K, Grue, K, Frias, ES, Pietrykowski, J, Jones, T, Nelson, G, et al., 2018. Female mice are protected from space radiation-induced maladaptive responses. Brain Behav. Immun. 74, 106-120. https://doi.org/10.1016/j.bbi.2018.08.008. · DOI
- Lei, F, Cui, N, Zhou, C, Chodosh, J, Vavvas, DG, Paschalis, EI, 2020. CSF1R inhibition by a small-molecule inhibitor is not microglia specific; affecting hematopoiesis and the function of macrophages. Proc. Natl. Acad. Sci. USA 117 (38), 23336-23338. https://doi.org/10.1073/pnas.1922788117. · DOI · Paper page
- Li, MD, Burns, TC, Kumar, S, Morgan, AA, Sloan, SA, Palmer, TD, 2015. Aging-like changes in the transcriptome of irradiated microglia. Glia 63 (5), 754-767. https:// doi.org/10.1002/glia.22782. · DOI
- Li, Q, Barres, BA, 2018. Microglia and macrophages in brain homeostasis and disease. Nat. Rev. Immunol. 18 (4), 225-242. https://doi.org/10.1038/nri.2017.125. · DOI · Paper page
- Liu, B, Hinshaw, RG, Le, KX, Park, MA, Wang, S, Belanger, AP, et al., 2019. Space-like (56)Fe irradiation manifests mild, early sex-specific behavioral and neuropathological changes in wildtype and Alzheimer's-like transgenic mice. Sci. Rep. 9 (1), 12118. https://doi.org/10.1038/s41598-019-48615-1. · DOI · Paper page
- Markarian, M, Krattli Jr., RP, Baddour, JD, Alikhani, L, Giedzinski, E, Usmani, MT, et al., 2021. Glia-selective deletion of complement C1q prevents radiation-induced cognitive deficits and neuroinflammation. Cancer Res. 81 (7), 1732-1744. https:// doi.org/10.1158/0008-5472.CAN-20-2565. · DOI
- Masuda, T, Amann, L, Sankowski, R, Staszewski, O, Lenz, M, P, DE, et al., 2020. Novel Hexb-based tools for studying microglia in the CNS. Nat. Immunol. 21 (7), 802-815. https://doi.org/10.1038/s41590-020-0707-4. · DOI · Paper page
- Mendes, MS, Le, L, Atlas, J, Brehm, Z, Ladron-de-Guevara, A, Matei, E, et al., 2021. The role of P2Y12 in the kinetics of microglial self-renewal and maturation in the adult visual cortex in vivo. Elife 10. https://doi.org/10.7554/eLife.61173. · DOI · Paper page
- Miry, O, Zhang, XL, Vose, LR, Gopaul, KR, Subah, G, Moncaster, JA, et al., 2021. Life- long brain compensatory responses to galactic cosmic radiation exposure. Sci. Rep. 11 (1), 4292. https://doi.org/10.1038/s41598-021-83447-y. · DOI
- Mizumatsu, S, Monje, ML, Morhardt, DR, Rola, R, Palmer, TD, Fike, JR, 2003. Extreme sensitivity of adult neurogenesis to low doses of X-irradiation. Cancer Res. 63 (14), 4021-4027.
- Monje, ML, Toda, H, Palmer, TD, 2003. Inflammatory blockade restores adult hippocampal neurogenesis. Science 302 (5651), 1760-1765. https://doi.org/ 10.1126/science.1088417. · DOI · Paper page
- Neher, JJ, Cunningham, C., 2019. Priming microglia for innate immune memory in the brain. Trends Immunol. 40 (4), 358-374. https://doi.org/10.1016/j.it.2019.02.001. · DOI
- Nimmerjahn, A, Kirchhoff, F, Helmchen, F, 2005. Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo. Science 308 (5726), 1314-1318. https://doi.org/10.1126/science.1110647. · DOI · Paper page
- Norbury, JW, Slaba, TC, Aghara, S, Badavi, FF, Blattnig, SR, Clowdsley, MS, et al., 2019. Advances in space radiation physics and transport at NASA. Life Sci. Space Res. 22, 98-124. https://doi.org/10.1016/j.lssr.2019.07.003. · DOI
- Paolicelli, RC, Bolasco, G, Pagani, F, Maggi, L, Scianni, M, Panzanelli, P, et al., 2011. Synaptic pruning by microglia is necessary for normal brain development. Science 333 (6048), 1456-1458. https://doi.org/10.1126/science.1202529. · DOI · Paper page
- Parihar, VK, Angulo, MC, Allen, BD, Syage, A, Usmani, MT, Passerat de la Chapelle, E, et al., 2020. Sex-specific cognitive deficits following space radiation exposure. Front. Behav. Neurosci. 14, 535885 https://doi.org/10.3389/fnbeh.2020.535885. · DOI · Paper page
- Parihar, VK, Limoli, CL., 2013. Cranial irradiation compromises neuronal architecture in the hippocampus. Proc. Natl. Acad. Sci. USA 110 (31), 12822-12827. https://doi. org/10.1073/pnas.1307301110. · DOI
- Parihar, VK, Pasha, J, Tran, KK, Craver, BM, Acharya, MM, Limoli, CL., 2015. Persistent changes in neuronal structure and synaptic plasticity caused by proton irradiation. Brain Struct. Funct. 220 (2), 1161-1171. https://doi.org/10.1007/s00429-014- 0709-9. · DOI
- Pariset, E, Malkani, S, Cekanaviciute, E, Costes, SV, 2021. Ionizing radiation-induced risks to the central nervous system and countermeasures in cellular and rodent models. Int. J. Radiat. Biol. 97 (sup1), S132-SS50. https://doi.org/10.1080/ 09553002.2020.1820598. · DOI
- Parkhurst, CN, Yang, G, Ninan, I, Savas, JN, Yates 3rd, JR, Lafaille, JJ, et al., 2013. Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor. Cell 155 (7), 1596-1609. https://doi.org/10.1016/j. cell.2013.11.030. · DOI · Paper page
- Perry, VH, Holmes, C., 2014. Microglial priming in neurodegenerative disease. Nat. Rev. Neurol. 10 (4), 217-224. https://doi.org/10.1038/nrneurol.2014. · DOI · Paper page
- Presumey, J, Bialas, AR, Carroll, MC, 2017. Complement system in neural synapse elimination in development and disease. Adv. Immunol. 135, 53-79. https://doi. org/10.1016/bs.ai.2017.06.004. · DOI
- Prinz, M, Masuda, T, Wheeler, MA, Quintana, FJ, 2021. Microglia and central nervous system-associated macrophages-from origin to disease modulation. Annu. Rev. Immunol. 39, 251-277. https://doi.org/10.1146/annurev-immunol-093019- 110159. · DOI · Paper page
- Raber, J, Allen, AR, Sharma, S, Allen, B, Rosi, S, Olsen, RH, et al., 2016. Effects of proton and combined proton and (56)Fe radiation on the hippocampus. Radiat. Res. 185 (1), 20-30. https://doi.org/10.1667/RR14222. · DOI
- Ransohoff, RM., 2016. A polarizing question: do M1 and M2 microglia exist? Nat. Neurosci. 19 (8), 987-991. https://doi.org/10.1038/nn.4338. · DOI · Paper page
- Rienecker, KDA, Paladini, MS, Grue, K, Krukowski, K, Microglia, Rosi S., 2021. Ally and enemy in deep space. Neurosci. Biobehav. Rev. 126, 509-514. https://doi.org/ 10.1016/j.neubiorev.2021.03.036. · DOI
- Rola, R, Fishman, K, Baure, J, Rosi, S, Lamborn, KR, Obenaus, A, et al., 2008. Hippocampal neurogenesis and neuroinflammation after cranial irradiation with (56)Fe particles. Radiat. Res. 169 (6), 626-632. https://doi.org/10.1667/RR1263. · DOI
- Schindler, MK, Forbes, ME, Robbins, ME, Riddle, DR., 2008. Aging-dependent changes in the radiation response of the adult rat brain. Int. J. Radiat. Oncol. Biol. Phys. 70 (3), 826-834. https://doi.org/10.1016/j.ijrobp.2007.10.054. · DOI
- Schroeder, MK, Liu, B, Hinshaw, RG, Park, MA, Wang, S, Dubey, S, et al., 2021. Long- term sex-and genotype-specific effects of (56)Fe irradiation on wild-type and APPswe/PS1dE9 transgenic mice. Int. J. Mol. Sci. 22 (24) https://doi.org/10.3390/ ijms222413305. · DOI
- Sierra, A, de Castro, F, Del Rio-Hortega, J, J, Rafael Iglesias-Rozas, Garrosa, M, The, Kettenmann H., 2016. Big-Bang" for modern glial biology: Translation and comments on Pio del Rio-Hortega 1919 series of papers on microglia. Glia 64 (11), 1801-1840. https://doi.org/10.1002/glia.23046. · DOI
- Sierra, A, Encinas, JM, Deudero, JJ, Chancey, JH, Enikolopov, G, Overstreet- Wadiche, LS, et al., 2010. Microglia shape adult hippocampal neurogenesis through apoptosis-coupled phagocytosis. Cell Stem Cell 7 (4), 483-495. https://doi.org/ 10.1016/j.stem.2010.08.014. · DOI · Paper page
- Stellwagen, D, Malenka, RC., 2006. Synaptic scaling mediated by glial TNF-alpha. Nature 440 (7087), 1054-1059. https://doi.org/10.1038/nature04671. · DOI · Paper page
- Stevens, B, Allen, NJ, Vazquez, LE, Howell, GR, Christopherson, KS, Nouri, N, et al., 2007. The classical complement cascade mediates CNS synapse elimination. Cell 131 (6), 1164-1178. https://doi.org/10.1016/j.cell.2007.10.036. · DOI · Paper page
- Stojiljkovic, MR, Schmeer, C, Witte, OW., 2022. Pharmacological depletion of microglia leads to a dose-dependent reduction in inflammation and senescence in the aged murine brain. Neuroscience 488, 1-9. https://doi.org/10.1016/j. neuroscience.2022.02.018. · DOI
- Sweet, TB, Hurley, SD, Wu, MD, Olschowka, JA, Williams, JP, O'Banion, MK, 2016. Neurogenic effects of low-dose whole-body HZE (Fe) ion and gamma irradiation. Radiat. Res. 186 (6), 614-623. https://doi.org/10.1667/RR14530. · DOI
- Sweet, TB, Panda, N, Hein, AM, Das, SL, Hurley, SD, Olschowka, JA, et al., 2014. Central nervous system effects of whole-body proton irradiation. Radiat. Res. 182 (1), 18-34. https://doi.org/10.1667/RR13699. · DOI
- Tan, YL, Yuan, Y, Tian, L, 2020. Microglial regional heterogeneity and its role in the brain. Mol. Psychiatry 25 (2), 351-367. https://doi.org/10.1038/s41380-019-0609- 8. · DOI · Paper page
- Task Group on Radiation Protection in Space IC, Dietze, G, Bartlett, DT, Cool, DA, Cucinotta, FA, Jia, X, et al., 2013. ICRP, 123. Assessment of Radiation Exposure of Astronauts in Space, 42. ICRP Publication, pp. 1-339. https://doi.org/10.1016/j. icrp.2013.05.004, 123. · DOI · Paper page
- Tay, TL, Savage, JC, Hui, CW, Bisht, K, Tremblay, ME, 2017. Microglia across the lifespan: from origin to function in brain development, plasticity and cognition. J. Physiol. 595 (6), 1929-1945. https://doi.org/10.1113/JP272134. · DOI · Paper page
- Tenner, AJ, Stevens, B, Woodruff, TM., 2018. New tricks for an ancient system: physiological and pathological roles of complement in the CNS. Mol. Immunol. 102, 3-13. 10.1016/j.molimm.2018.06.264. · DOI
- Tremblay, ME, Lowery, RL, Majewska, AK., 2010. Microglial interactions with synapses are modulated by visual experience. PLoS Biol. 8 (11), e1000527 https://doi.org/ 10.1371/journal.pbio.1000527. · DOI · Paper page
- Turnquist, C, Beck, JA, Horikawa, I, Obiorah, IE, Von Muhlinen, N, Vojtesek, B, et al., 2019. Radiation-induced astrocyte senescence is rescued by Delta133p53. Neuro Oncol. 21 (4), 474-485. https://doi.org/10.1093/neuonc/noz001. · DOI · Paper page
- Willis, EF, MacDonald, KPA, Nguyen, QH, Garrido, AL, Gillespie, ER, Harley, SBR, et al., 2020. Repopulating Microglia Promote Brain Repair in an IL-6-Dependent Manner. Cell 180 (5), 833-846. https://doi.org/10.1016/j.cell.2020.02.013 e16. · DOI · Paper page
- Wolf, SA, Boddeke, HW, Kettenmann, H., 2017. Microglia in physiology and disease. Annu. Rev. Physiol. 79, 619-643. https://doi.org/10.1146/annurev-physiol- 022516-034406. · DOI · Paper page
- Wright-Jin, EC, Gutmann, DH., 2019. Microglia as dynamic cellular mediators of brain function. Trends Mol. Med. 25 (11), 967-979. https://doi.org/10.1016/j. molmed.2019.08.013. · DOI
- Youm, YH, Grant, RW, McCabe, LR, Albarado, DC, Nguyen, KY, Ravussin, A, et al., 2013. Canonical Nlrp3 inflammasome links systemic low-grade inflammation to functional decline in aging. Cell Metab. 18 (4), 519-532. https://doi.org/10.1016/j. cmet.2013.09.010. · DOI · Paper page
Cited by
Sorted by citations
Dynan, W. S., Chang, P. Y., Sishc, B. J., & Elgart, S. R. (2022) · Life Sciences in Space Research · doi:10.1016/j.lssr.2022.10.003 · Cited by 12 · see citing works
- Authors
- Kerry O'Banion, M.
- ORCID
- Kerry O'Banion, M.
- Venue
- Life Sciences in Space Research
- Publisher
- Elsevier BV
- Published
- 2022-11
- Volume
- 35
- Pages
- 180-186
- ISSN
- 2214-5524 (ISSN-L)
- OpenAlex
- W4291097451
- Cited by
- 10
- References
- 26
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 5 · 2022: 1
- FWCI
- 0.23
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Life Sciences in Space Research (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (R56 AG066397)
- National Aeronautics and Space Administration (80NSSC21K0542)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Physiology › Spaceflight effects on biology
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Keywords
- microglia, space radiation, late radiation effects, central nervous system, microglial dysfunction, neuroinflammation, neurodegenerative diseases, aging, neurogenesis, synaptic plasticity, phagocytosis, radiation mitigation, deep space exploration
- MeSH terms
- Brain, Humans, Radiation Injuries, Microglia, Neurodegenerative Diseases
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