Diverged morphology changes of astrocytic and neuronal primary cilia under reactive insults

Molecular Brain - Tập 13 - Trang 1-16 - 2020
Ashley Sterpka1, Juan Yang1, Matthew Strobel1, Yuxin Zhou1, Connor Pauplis1, Xuanmao Chen1
1Department of Molecular, Cellular and Biomedical Sciences, College of Life Sciences and Agriculture, University of New Hampshire, Durham, USA

Tóm tắt

Primary cilia are centriole-derived sensory organelles that are present in most mammalian cells, including astrocytes and neurons. Evidence is emerging that astrocyte and neuronal primary cilia demonstrate a dichotomy in the mature mouse brain. However, it is unknown how astrocytic and neuronal primary cilia change their morphology and ciliary proteins when exposed to reactive insults including epilepsy and traumatic brain injury. We used a double transgenic mouse strain (Arl13b-mCherry; Centrin2-GFP), in which we found spontaneous seizures, and a cortical injury model to examine the morphological changes of astrocytic and neuronal primary cilia under reactive conditions. Transgenic overexpression of Arl13b drastically increases the length of astrocytic and neuronal primary cilia in the hippocampus, as well as the cilia lengths of cultured astrocytes and neurons. Spontaneous seizures shorten Arl13b-positive astrocytic cilia and AC3-positive neuronal cilia in the hippocampus. In a cortical injury model, Arl13b is not detectable in primary cilia, but Arl13b protein relocates to the cell body and has robust expression in the proximity of injured tissues. In contrast, the number of AC3-positive cilia near injured tissues remains unchanged, but their lengths become shorter. These results on astrocytic cilia implicate Arl13b in regulating astrocyte proliferation and tissue regeneration, while the shortening of AC3-positive cilia suggests adaptive changes of neuronal primary cilia under excitotoxicity.

Tài liệu tham khảo

Sterpka A, Chen X. Neuronal and astrocytic primary cilia in the mature brain. Pharmacol Res. 2018;137:114–21.. Singla V, Reiter JF. The primary cilium as the cell's antenna: signaling at a sensory organelle. Science. 2006;313(5787):629–33. Pan J, Snell W. The primary cilium: keeper of the key to cell division. Cell. 2007;129(7):1255–7. Qiu L, et al. Type 3 adenylyl cyclase: a key enzyme mediating the cAMP signaling in neuronal cilia. Int J Physiol Pathophysiol Pharmacol. 2016;8(3):95–108. Koemeter-Cox AI, et al. Primary cilia enhance kisspeptin receptor signaling on gonadotropin-releasing hormone neurons. Proc Natl Acad Sci U S A. 2014;111(28):10335–40. Phua SC, et al. Dynamic remodeling of membrane composition drives cell cycle through primary cilia excision. Cell. 2019;178(1):261. Malicki JJ, Johnson CA. The cilium: cellular antenna and central processing unit. Trends Cell Biol. 2017;27(2):126–40. Veland IR, Lindbaek L, Christensen ST. Linking the primary cilium to cell migration in tissue repair and brain development. Bioscience. 2014;64(12):1115–25. Anvarian Z, et al. Cellular signalling by primary cilia in development, organ function and disease. Nat Rev Nephrol. 2019;15(4):199–219. Babu D, Roy S. Left-right asymmetry: cilia stir up new surprises in the node. Open Biol. 2013;3(5):130052. Pazour GJ, Witman GB. The vertebrate primary cilium is a sensory organelle. Curr Opin Cell Biol. 2003;15(1):105–10. Guemez-Gamboa A, Coufal NG, Gleeson JG. Primary cilia in the developing and mature brain. Neuron. 2014;82(3):511–21. Vaisse C, Reiter JF, Berbari NF. Cilia and Obesity. Cold Spring Harb Perspect Biol. 2017;9(7). Valente EM, et al. Primary cilia in neurodevelopmental disorders. Nat Rev Neurol. 2014;10(1):27–36. Loskutov YV, et al. LPA signaling is regulated through the primary cilium: a novel target in glioblastoma. Oncogene. 2018;37(11):1457–71. Alvarez-Satta M, Matheu A. Primary cilium and glioblastoma. Ther Adv Med Oncol. 2018;10:1758835918801169. Kasahara K, et al. Visualization of astrocytic primary cilia in the mouse brain by immunofluorescent analysis using the cilia marker Arl13b. Acta Med Okayama. 2014;68(6):317–22. Bishop GA, et al. Type III adenylyl cyclase localizes to primary cilia throughout the adult mouse brain. J Comp Neurol. 2007;505(5):562–71. Myster DL, Duronio RJ. To differentiate or not to differentiate? Curr Biol. 2000;10(8):R302–4. Schou KB, Pedersen LB, Christensen ST. Ins and outs of GPCR signaling in primary cilia. EMBO Rep. 2015;16(9):1099–113. Chen X, Xia Z, Storm DR. Stimulation of electro-olfactogram responses in the main olfactory epithelia by airflow depends on the type 3 adenylyl cyclase. J Neurosci. 2012;32(45):15769–78. Chen X, et al. Ablation of type III adenylyl Cyclase in mice causes reduced neuronal activity, altered sleep pattern, and depression-like phenotypes. Biol Psychiatry. 2016;80(11):836–48. Sofroniew MV, Vinters HV. Astrocytes: biology and pathology. Acta Neuropathol. 2010;119(1):7–35. Schiweck J, Eickholt BJ, Murk K. Important Shapeshifter: mechanisms allowing astrocytes to respond to the changing nervous system during development, Injury and Disease. Front Cell Neurosci. 2018;12:261. Perea G, Navarrete M, Araque A. Tripartite synapses: astrocytes process and control synaptic information. Trends Neurosci. 2009;32(8):421–31. Higginbotham H, et al. Arl13b in primary cilia regulates the migration and placement of interneurons in the developing cerebral cortex. Dev Cell. 2012;23(5):925–38. Larkins CE, et al. Arl13b regulates ciliogenesis and the dynamic localization of Shh signaling proteins. Mol Biol Cell. 2011;22(23):4694–703. Mariani LE, et al. Arl13b regulates Shh signaling from both inside and outside the cilium. Mol Biol Cell. 2016. Nozaki S, et al. Regulation of ciliary retrograde protein trafficking by the Joubert syndrome proteins ARL13B and INPP5E. J Cell Sci. 2017;130(3):563–76. Jakel S, Dimou L. Glial cells and their function in the adult brain: a journey through the history of their ablation. Front Cell Neurosci. 2017;11:24. Mangia S, et al. The in vivo neuron-to-astrocyte lactate shuttle in human brain: evidence from modeling of measured lactate levels during visual stimulation. J Neurochem. 2009;109(Suppl 1):55–62. Wang H, et al. Portrait of glial scar in neurological diseases. Int J Immunopathol Pharmacol. 2018;31:2058738418801406. Bangs FK, et al. Lineage specificity of primary cilia in the mouse embryo. Nat Cell Biol. 2015;17(2):113–22. Bernet A, et al. Cell-lineage specificity of primary cilia during postnatal epididymal development. Hum Reprod. 2018;33(10):1829–38. Kim YK, et al. Localization of primary cilia in mouse retina. Acta Histochem. 2013;115(8):789–94. Van Erum J, Van Dam D, De Deyn PP. PTZ-induced seizures in mice require a revised Racine scale. Epilepsy Behav. 2019;95:51–5. Phelan KD, et al. Pilocarpine-induced status epilepticus in mice: a comparison of spectral analysis of electroencephalogram and behavioral grading using the Racine scale. Epilepsy Res. 2015;117:90–6. Chen X, et al. Diarylamidines: high potency inhibitors of acid-sensing ion channels. Neuropharmacology. 2010;58(7):1045–53. Guadiana SM, et al. Type 3 adenylyl Cyclase and Somatostatin receptor 3 expression persists in aged rat neocortical and hippocampal neuronal cilia. Front Aging Neurosci. 2016;8:127. Wang WJ, et al. The conversion of centrioles to centrosomes: essential coupling of duplication with segregation. J Cell Biol. 2011;193(4):727–39. Delaval B, et al. Centrin depletion causes cyst formation and other ciliopathy-related phenotypes in zebrafish. Cell Cycle. 2011;10(22):3964–72. Ying G, et al. Centrin 2 is required for mouse olfactory ciliary trafficking and development of ependymal cilia planar polarity. J Neurosci. 2014;34(18):6377–88. Mullee LI, Morrison CG. Centrosomes in the DNA damage response--the hub outside the Centre. Chromosom Res. 2016;24(1):35–51. Bose A, Dalal SN. 14–3-3 proteins mediate the localization of Centrin2 to centrosome. J Biosci. 2019;44(2). Farrell JS, Wolff MD, Teskey GC. Neurodegeneration and pathology in epilepsy: clinical and basic perspectives. Adv Neurobiol. 2017;15:317–34. Rossi AR, et al. Gabapentin administration reduces reactive gliosis and neurodegeneration after pilocarpine-induced status epilepticus. PLoS One. 2013;8(11):e78516. Eng LF, Ghirnikar RS. GFAP and astrogliosis. Brain Pathol. 1994;4(3):229–37. Li K, et al. Reactive astrocytes in neurodegenerative diseases. Aging Dis. 2019;10(3):664–75. Liddelow SA, Barres BA. Reactive astrocytes: production, function, and therapeutic potential. Immunity. 2017;46(6):957–67. Zhang S, et al. GFAP expression in injured astrocytes in rats. Exp Ther Med. 2017;14(3):1905–8. Chen Y, Swanson RA. Astrocytes and brain injury. J Cereb Blood Flow Metab. 2003;23(2):137–49. Balasingam V, et al. Reactive astrogliosis in the neonatal mouse brain and its modulation by cytokines. J Neurosci. 1994;14(2):846–56. Miyake T, et al. Quantitative studies on proliferative changes of reactive astrocytes in mouse cerebral cortex. Brain Res. 1988;451(1–2):133–8. Goelz MF, et al. Neuropathologic findings associated with seizures in FVB mice. Lab Anim Sci. 1998;48(1):34–7. Wetherington J, Serrano G, Dingledine R. Astrocytes in the epileptic brain. Neuron. 2008;58(2):168–78. Kohnken RA, Schwahn DJ. Lack of chronic histologic lesions supportive of sublethal spontaneous seizures in FVB/N mice. Comp Med. 2016;66(2):105–11. Silva-Fernandes A, Pedro O, Nuno S, Patricia M. Motor and Behavioural Abnormalities Associated with Persistent Spontaneous Epilepsy in the fvb/n Mouse Strain. Scand J Lab Anim Sci. 2010;37:213–22. Kirschen GW, et al. The radial organization of neuronal primary cilia is acutely disrupted by seizure and ischemic brain injury. Front Biol (Beijing). 2017;12(2):124–38. Verkhratsky A, et al. Neurological diseases as primary gliopathies: a reassessment of neurocentrism. ASN Neuro. 2012;4(3). Sofroniew MV. Astrogliosis. Cold Spring Harb Perspect Biol. 2015;7(2):a020420. Sofroniew MV. Astrocyte barriers to neurotoxic inflammation. Nat Rev Neurosci. 2015;16(5):249–63. Pekny M, Pekna M. Astrocyte reactivity and reactive astrogliosis: costs and benefits. Physiol Rev. 2014;94(4):1077–98. Ge WP, Jia JM. Local production of astrocytes in the cerebral cortex. Neuroscience. 2016;323:3–9. Tian GF, et al. An astrocytic basis of epilepsy. Nat Med. 2005;11(9):973–81. Oberheim NA, et al. Loss of astrocytic domain organization in the epileptic brain. J Neurosci. 2008;28(13):3264–76. Burda JE, Bernstein AM, Sofroniew MV. Astrocyte roles in traumatic brain injury. Exp Neurol. 2016;275(Pt 3):305–15. Burda JE, Sofroniew MV. Reactive gliosis and the multicellular response to CNS damage and disease. Neuron. 2014;81(2):229–48. Pekny M, et al. Astrocytes: a central element in neurological diseases. Acta Neuropathol. 2016;131(3):323–45. Pekny M, Nilsson M. Astrocyte activation and reactive gliosis. Glia. 2005;50(4):427–34. Cantagrel V, et al. Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. Am J Hum Genet. 2008;83(2):170–9. Roy K, et al. Palmitoylation of the ciliary GTPase ARL13b is necessary for its stability and its role in cilia formation. J Biol Chem. 2017;292(43):17703–17. Bay SN, Long AB, Caspary T. Disruption of the ciliary GTPase Arl13b suppresses sonic hedgehog overactivation and inhibits medulloblastoma formation. Proc Natl Acad Sci U S A. 2018;115(7):1570–5. Ribes V, Briscoe J. Establishing and interpreting graded sonic hedgehog signaling during vertebrate neural tube patterning: the role of negative feedback. Cold Spring Harb Perspect Biol. 2009;1(2):a002014. Pal K, Mukhopadhyay S. Primary cilium and sonic hedgehog signaling during neural tube patterning: role of GPCRs and second messengers. Dev Neurobiol. 2015;75(4):337–48. Heussler HS, et al. Extreme variability of expression of a sonic hedgehog mutation: attention difficulties and holoprosencephaly. Arch Dis Child. 2002;86(4):293–6. Tsukui T, et al. Multiple left-right asymmetry defects in Shh(−/−) mutant mice unveil a convergence of the shh and retinoic acid pathways in the control of Lefty-1. Proc Natl Acad Sci U S A. 1999;96(20):11376–81. Roessler E, et al. Mutations in the human sonic hedgehog gene cause holoprosencephaly. Nat Genet. 1996;14(3):357–60. Amankulor NM, et al. Sonic hedgehog pathway activation is induced by acute brain injury and regulated by injury-related inflammation. J Neurosci. 2009;29(33):10299–308.