(1) Hirsch, E. C.; Hunot, S. Neuroinflammation in Parkinson’s Disease: A Target for Neuroprotection? Lancet. Neurol.2009, 8 (4), 382.
(2) Krause, D. L.; Müller, N. Neuroinflammation, Microglia and Implications for Anti-Inflammatory Treatment in Alzheimer’s Disease. Int. J. Alzheimers. Dis.2010, 2010, 732806.
(3) Musella, A.; Gentile, A.; Rizzo, F. R.; Vito, F. De; Fresegna, D.; Bullitta, S.; Vanni, V.; Guadalupi, L.; Bassi, M. S.; Buttari, F.; Centonze, D.; Mandolesi, G. Interplay between Age and Neuroinflammation in Multiple Sclerosis: Effects on Motor and Cognitive Functions. Front. Aging Neurosci.2018, 10, 1.
(4) Guzman-martinez, L.; Maccioni, R. B.; Andrade, V.; Navarrete, L. P.; Pastor, M. G.; Ramos-escobar, N. Neuroinflammation as a Common Feature of Neurodegenerative Disorders. Front. Pharmarcol.2019, 10, 1.
(5) Walker, D. G.; Yasuhara, O.; Patston, P. A.; McGeer, E. G.; McGeer, P. L. Complement C1 Inhibitor Is Produced by Brain Tissue and Is Cleaved in Alzheimer’s Disease. Brain Res.1995, 675 (1), 75.
(6) Thomas, A.; Gasque, P.; Vaudry, D.; Gonzalez, B.; Fontaine, M. Expression of a Complete and Functional Complement System by Human Neuronal Cells in Vitro. Int. Immunol.2000, 12 (7), 1015–1023.
(7) Gasque, P.; Chan, P.; Mauger, C.; Schouft, M. T.; Singhrao, S.; Dierich, M. P.; Morgan, B. P.; Fontaine, M. Identification and Characterization of Complement C3 Receptors on Human Astrocytes. J. Immunol.1996, 156 (6), 2247.
(8) Walker, D. G.; Kim, S. U.; McGeer, P. L. Complement and Cytokine Gene Expression in Cultured Microglia Derived from Postmortem Human Brains. J. Neurosci. Res.1995, 40 (4), 478.
(9) Norden, D. M.; Godbout, J. P. Review: Microglia of the Aged Brain: Primed to Be Activated and Resistant to Regulation. Neuropathol. Appl. Neurobiol.2013, 39 (1), 19.
(10) DiSabato, D. J.; Quan, N.; Godbout, J. P. Neuroinflammation: The Devil Is in the Details. J. Neurochem.2016, 139, 136.
(11) Laflamme, N.; Rivest, S. Toll-like Receptor 4: The Missing Link of the Cerebral Innate Immune Response Triggered by Circulating Gram-Negative Bacterial Cell Wall Components. FASEB J. Off. Publ. Fed. Am. Soc. Exp. Biol.2001, 15 (1), 155.
(12) Lehnardt, S.; Lachance, C.; Patrizi, S.; Lefebvre, S.; Follett, P. L.; Jensen, F. E.; Rosenberg, P. A.; Volpe, J. J.; Vartanian, T. The Toll-like Receptor TLR4 Is Necessary for Lipopolysaccharide-Induced Oligodendrocyte Injury in the CNS. J. Neurosci.2002, 22 (7), 2478.
(13) Shen, Y.; Qin, H.; Chen, J.; Mou, L.; He, Y.; Yan, Y.; Zhou, H.; Lv, Y.; Chen, Z.; Wang, J.; Zhou, Y.-D. Postnatal Activation of TLR4 in Astrocytes Promotes Excitatory Synaptogenesis in Hippocampal Neurons. J. Cell Biol.2016, 215 (5), 719.
(14) Acosta, C.; Davies, A. Bacterial Lipopolysaccharide Regulates Nociceptin Expression in Sensory Neurons. J. Neurosci. Res.2008, 86 (5), 1077.
(15) Chistyakov, D. V; Azbukina, N. V; Lopachev, A. V; Kulichenkova, K. N.; Astakhova, A. A.; Sergeeva, M. G. Rosiglitazone as a Modulator of TLR4 and TLR3 Signaling Pathways in Rat Primary Neurons and Astrocytes. Int. J. Mol. Sci.2018, 19 (1).
(16) Kacimi, R.; Giffard, R. G.; Yenari, M. A. Endotoxin-Activated Microglia Injure Brain Derived Endothelial Cells via NF-ΚB, JAK-STAT and JNK Stress Kinase Pathways. J. Inflamm. (Lond).2011, 8, 7.
(17) Park, B. S.; Lee, J.-O. Recognition of Lipopolysaccharide Pattern by TLR4 Complexes. Exp. Mol. Med.2013, 45 (12), e66.
(18) Bing, G.; Liu, M. Lipopolysaccharide Animal Models for Parkinson’s Disease. Parkinsons. Dis.2011, 2011, 327089.
(19) Zakaria, R.; Wan Yaacob, W. M.; Othman, Z.; Long, I.; Ahmad, A. H.; Al-Rahbi, B. Lipopolysaccharide-Induced Memory Impairment in Rats: A Model of Alzheimer’s Disease. Physiol. Res.2017, 66 (4), 553.
(20) Batista, C. R. A.; Gomes, G. F.; Candelario-Jalil, E.; Fiebich, B. L.; de Oliveira, A. C. P. Lipopolysaccharide-Induced Neuroinflammation as a Bridge to Understand Neurodegeneration. Int. J. Mol. Sci.2019, 20 (9), 2293.
(21) Zhao, J.; Bi, W.; Xiao, S.; Lan, X.; Cheng, X.; Zhang, J.; Lu, D.; Wei, W.; Wang, Y.; Li, H.; Fu, Y.; Zhu, L. Neuroinflammation Induced by Lipopolysaccharide Causes Cognitive Impairment in Mice. Sci. Rep.2019, 9 (1), 5790.
(22) Catorce, M. N.; Gevorkian, G. LPS-Induced Murine Neuroinflammation Model: Main Features and Suitability for Pre-Clinical Assessment of Nutraceuticals. Curr. Neuropharmacol.2016, 14 (2), 155.
(23) Hunter, R. L.; Cheng, B.; Choi, D. Y.; Liu, M.; Liu, S.; Cass, W. A.; Bing, G. Intrastriatal Lipopolysaccharide Injection Induces Parkinsonism in C57/B6 Mice. J. Neurosci. Res.2009, 87 (8), 1913.
(24) Deng, X.; Li, M.; Ai, W.; He, L.; Lu, D.; Patrylo, P. R.; Cai, H.; Luo, X.; Li, Z.; Yan, X. Lipolysaccharide-Induced Neuroinflammation Is Associated with Alzheimer-Like Amyloidogenic Axonal Pathology and Dendritic Degeneration in Rats. Adv. Alzheimer’s Dis.2014, 3 (2), 78.
(25) Hoban, D. B.; Connaughton, E.; Connaughton, C.; Hogan, G.; Thornton, C.; Mulcahy, P.; Moloney, T. C.; Dowd, E. Further Characterisation of the LPS Model of Parkinson’s Disease: A Comparison of Intra-Nigral and Intra-Striatal Lipopolysaccharide Administration on Motor Function, Microgliosis and Nigrostriatal Neurodegeneration in the Rat. Brain. Behav. Immun.2013, 27 (1), 91.
(26) Essentials of Glycobiology; Varki, A., Cummings, R. D., Esko, J. D., Freeze, H. H., Stanley, P., Bertozzi, C. R., Hart, G. W., Etzler, M. E., Eds.; Cold Spring Harbour Laboratory Press: New York, NY, 2009.
(27) Apweiler, R.; Hermjakob, H.; Sharon, N. On the Frequency of Protein Glycosylation, as Deduced from Analysis of the SWISS-PROT Database. Biochim. Biophys. Acta1999, 1473 (1), 4.
(28) Helenius, A.; Aebi, M. Intracellular Functions of N-Linked Glycans. Science (80-. ).2001, 291 (5512), 2364.
(29) Kornfeld, R.; Kornfeld, S. Assembly of Asparagine-Linked Oligosaccharides. Annu. Rev. Biochem.1985, 54, 631.
(30) Scott, H.; Panin, V. M. N-Glycosylation in Regulation of the Nervous System. Adv. Neurobiol.2014, 9, 367.
(31) Jaeken, J.; Carchon, H. Congenital Disorders of Glycosylation: A Booming Chapter of Pediatrics. Curr. Opin. Pediatr.2004, 16 (4), 434.
(32) Rebelo, A. L.; Chevalier, M. T.; Russo, L.; Pandit, A. Sweet Tailoring of Glyco-Modulatory Extracellular Matrix-Inspired Biomaterials to Target Neuroinflammation. Cell Reports Phys. Sci.2021, 2 (2), 100321.
(33) Werneburg, S.; Mühlenhoff, M.; Stangel, M.; Hildebrandt, H. Polysialic Acid on SynCAM 1 in NG2 Cells and on Neuropilin-2 in Microglia Is Confined to Intracellular Pools That Are Rapidly Depleted upon Stimulation. Glia2015, 63 (7), 1240.
(34) Sumida, M.; Hane, M.; Yabe, U.; Shimoda, Y.; Pearce, O. M. T.; Kiso, M.; Miyagi, T.; Sawada, M.; Varki, A.; Kitajima, K.; Sato, C. Rapid Trimming of Cell Surface Polysialic Acid (PolySia) by Exovesicular Sialidase Triggers Release of Preexisting Surface Neurotrophin. J. Biol. Chem.2015, 290 (21), 13202.
(35) Demina, E. P.; Pierre, W. C.; Nguyen, A. L. A.; Londono, I.; Reiz, B.; Zou, C.; Chakraberty, R.; Cairo, C. W.; Pshezhetsky, A. V; Lodygensky, G. A. Persistent Reduction in Sialylation of Cerebral Glycoproteins Following Postnatal Inflammatory Exposure. J. Neuroinflammation2018, 15 (1), 336.
(36) Paxinos, G.; Watson, C. The Rat Brain in Stereotaxic Coordinates, 4th ed.; Academic Press, 1998.
(37) Kuhnast, B.; Damont, A.; Hinnen, F.; Catarina, T.; Demphel, S.; Le Helleix, S.; Coulon, C.; Goutal, S.; Gervais, P.; Dollé, F. [ 18F]DPA-714, [ 18F]PBR111 and [ 18F]FEDAA1106-Selective Radioligands for Imaging TSPO 18kDa with PET: Automated Radiosynthesis on a TRACERLAb FX-FN Synthesizer and Quality Controls. Appl. Radiat. Isot.2012, 70 (3), 489.
(38) Lavisse, S.; Guillermier, M.; Hérard, A. S.; Petit, F.; Delahaye, M.; Van Camp, N. V.; Haim, L. Ben; Lebon, V.; Remy, P.; Dollé, F.; Delzescaux, T.; Bonvento, G.; Hantraye, P.; Escartin, C. Reactive Astrocytes Overexpress TSPO and Are Detected by TSPO Positron Emission Tomography Imaging. J. Neurosci.2012, 32 (32), 10809.
(39) Ichise, M.; Ballinger, J. R.; Golan, H.; Vines, D.; Luong, A.; Tsai, S.; Kung, H. F. Noninvasive Quantification of Dopamine D2 Receptors with Iodine-123-IBF SPECT. J. Nucl. Med.1996, 37 (3), 513–520.
(40) Cresto, N.; Gaillard, M. C.; Gardier, C.; Gubinelli, F.; Diguet, E.; Bellet, D.; Legroux, L.; Mitja, J.; Auregan, G.; Guillermier, M.; Josephine, C.; Jan, C.; Dufour, N.; Joliot, A.; Hantraye, P.; Bonvento, G.; Déglon, N.; Bemelmans, A. P.; Cambon, K.; Liot, G.; Brouillet, E. The C-Terminal Domain of LRRK2 with the G2019S Mutation Is Sufficient to Produce Neurodegeneration of Dopaminergic Neurons in Vivo. Neurobiol. Dis.2020, 134, 104614.
(41) Samal, J.; Saldova, R.; Rudd, P. M.; Pandit, A.; Flaherty, R. O. Region-Specific Characterization of N -Glycans in Striatum and Substantia Nigra of an Adult Rodent Brain. Anal. Chem.2020, 92(19), 12842.
(42) Küster, B.; Wheeler, S. F.; Hunter, A. P.; Dwek, R. A.; Harvey, D. J. Sequencing of N-Linked Oligosaccharides Directly from Protein Gels: In-Gel Deglycosylation Followed by Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry and Normal-Phase High-Performance Liquid Chromatography. Anal. Biochem.1997, 250 (1), 82.
(43) Bigge, J. C.; Patel, T. P.; Bruce, J. A.; Goulding, P. N.; Charles, S. M.; Parekh, R. B. Nonselective and Efficient Fluorescent Labeling of Glycans Using 2-Amino Benzamide and Anthranilic Acid. Anal. Biochem.1995, 230 (2), 229.
(44) Royle, L.; Radcliffe, C. M.; Dwek, R. A.; Rudd, P. M. Detailed Structural Analysis of N-Glycans Released from Glycoproteins in SDS-PAGE Gel Bands Using HPLC Combined with Exoglycosidase Array Digestions. Methods Mol. Biol.2006, 347, 125.
(45) Royle, L.; Campbell, M. P.; Radcliffe, C. M.; White, D. M.; Harvey, D. J.; Abrahams, J. L.; Kim, Y.-G.; Henry, G. W.; Shadick, N. A.; Weinblatt, M. E.; Lee, D. M.; Rudd, P. M.; Dwek, R. A. HPLC-Based Analysis of Serum N-Glycans on a 96-Well Plate Platform with Dedicated Database Software. Anal. Biochem.2008, 376 (1), 1.
(46) Angel, P. M.; Mehta, A.; Norris-Caneda, K.; Drake, R. R. MALDI Imaging Mass Spectrometry of N-Glycans and Tryptic Peptides from the Same Formalin-Fixed, Paraffin-Embedded Tissue Section. Methods Mol. Biol.2018, 1788, 225.
(47) McDowell, C. T.; Klamer, Z.; Hall, J.; West, C. A.; Wisniewski, L.; Powers, T. W.; Angel, P. M.; Mehta, A. S.; Lewin, D. N.; Haab, B. B.; Drake, R. R. Imaging Mass Spectrometry and Lectin Analysis of N-Linked Glycans in Carbohydrate Antigen Defined Pancreatic Cancer Tissues. Mol. Cell. Proteomics2021, in press, doi: 10.1074/mcp.RA120.002256.
(48) Lu, X.; Zhang, D.; Shoji, H.; Duan, C.; Zhang, G.; Isaji, T.; Wang, Y.; Fukuda, T.; Gu, J. Deficiency of Α1,6-Fucosyltransferase Promotes Neuroinflammation by Increasing the Sensitivity of Glial Cells to Inflammatory Mediators. Biochim. Biophys. Acta - Gen. Subj.2019, 1863 (3), 598.
(49) Powers, T. W.; Jones, E. E.; Betesh, L. R.; Romano, P. R.; Gao, P.; Copland, J. A.; Mehta, A. S.; Drake, R. R. Matrix Assisted Laser Desorption Ionization Imaging Mass Spectrometry Workflow for Spatial Profiling Analysis of N-Linked Glycan Expression in Tissues. Anal. Chem.2013, 85 (20), 9799.
(50) Nishikaze, T. Sensitive and Structure-Informative N-Glycosylation Analysis by MALDI-MS; Ionization, Fragmentation, and Derivatization. Mass Spectrom.2017, 6 (1), A0060.
(51) Wheeler, S. F.; Domann, P.; Harvey, D. J. Derivatization of Sialic Acids for Stabilization in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry and Concomitant Differentiation of α(2 → 3)- and α(2 → 6)-Isomers. Rapid Commun. Mass Spectrom.2009, 23 (2), 303.
(52) Kleene, R.; Schachner, M. Glycans and Neural Cell Interactions. Nat. Rev. Neurosci.2004, 5 (3), 195.
(53) Chang, I. J.; He, M.; Lam, C. T. Congenital Disorders of Glycosylation. Ann. Transl. Med.2018, 6 (24), 477.
(54) Furube, E.; Kawai, S.; Inagaki, H.; Takagi, S.; Miyata, S. Brain Region-Dependent Heterogeneity and Dose-Dependent Difference in Transient Microglia Population Increase during Lipopolysaccharide-Induced Inflammation. Sci. Rep.2018, 8 (1), 2203.
(55) Yao, R.; Pan, R.; Shang, C.; Li, X.; Cheng, J.; Xu, J.; Li, Y. Translocator Protein 18 KDa (TSPO) Deficiency Inhibits Microglial Activation and Impairs Mitochondrial Function. Front. Pharmacol.2020, 11, 986.
(56) Liddelow, S. A.; Guttenplan, K. A.; Clarke, L. E.; Bennett, F. C.; Bohlen, C. J.; Schirmer, L.; Bennett, M. L.; Münch, A. E.; Chung, W. S.; Peterson, T. C.; Wilton, D. K.; Frouin, A.; Napier, B. A.; Panicker, N.; Kumar, M.; Buckwalter, M. S.; Rowitch, D. H.; Dawson, V. L.; Dawson, T. M.; Stevens, B.; Barres, B. A. Neurotoxic Reactive Astrocytes Are Induced by Activated Microglia. Nature2017, 541 (7638), 481.
(57) Kim, Y. S.; Joh, T. H. Microglia, Major Player in the Brain Inflammation: Their Roles in the Pathogenesis of Parkinson’s Disease. Exp. Mol. Med.2006, 38 (4), 333.
(58) Szepesi, Z.; Manouchehrian, O.; Bachiller, S.; Deierborg, T. Bidirectional Microglia–Neuron Communication in Health and Disease. Front. Cell. Neurosci.2018, 12, 323.
(59) Holness, C. L.; Simmons, D. L. Molecular Cloning of CD68, a Human Macrophage Marker Related to Lysosomal Glycoproteins. Blood1993, 81 (6), 1607.
(60) Ory, D.; Planas, A.; Dresselaers, T.; Gsell, W.; Postnov, A.; Celen, S.; Casteels, C.; Himmelreich, U.; Debyser, Z.; Van Laere, K.; Verbruggen, A.; Bormans, G. PET Imaging of TSPO in a Rat Model of Local Neuroinflammation Induced by Intracerebral Injection of Lipopolysaccharide. Nucl. Med. Biol.2015, 42 (10), 753.
(61) Beier, E. E.; Neal, M.; Alam, G.; Edler, M.; Wu, L.-J.; Richardson, J. R. Alternative Microglial Activation Is Associated with Cessation of Progressive Dopamine Neuron Loss in Mice Systemically Administered Lipopolysaccharide. Neurobiol. Dis.2017, 108, 115.
(62) Herrera, A. J.; Castaño, A.; Venero, J. L.; Cano, J.; Machado, A. The Single Intranigral Injection of LPS as a New Model for Studying the Selective Effects of Inflammatory Reactions on Dopaminergic System. Neurobiol. Dis.2000, 7 (4), 429.
(63) Han, L.; Zhang, D.; Tao, T.; Sun, X.; Liu, X.; Zhu, G.; Xu, Z.; Zhu, L.; Zhang, Y.; Liu, W.; Ke, K.; Shen, A. The Role of N-Glycan Modification of TNFR1 in Inflammatory Microglia Activation. Glycoconj. J.2015, 32 (9), 685.
(64) Kontou, M.; Weidemann, W.; Bork, K.; Horstkorte, R. Beyond Glycosylation: Sialic Acid Precursors Act as Signaling Molecules and Are Involved in Cellular Control of Differentiation of PC12 Cells. Biol. Chem.2009, 390 (7), 575.
(65) Quirico-Santos, T.; Fonseca, C. O.; Lagrota-Candido, J. Brain Sweet Brain: Importance of Sugars for the Cerebral Microenvironment and Tumor Development. Arq. Neuropsiquiatr.2010, 68, 799.
(66) Isaev, D.; Isaeva, E.; Shatskih, T.; Zhao, Q.; Smits, N. C.; Shworak, N. W.; Khazipov, R.; Holmes, G. L. Role of Extracellular Sialic Acid in Regulation of Neuronal and Network Excitability in the Rat Hippocampus. J. Neurosci.2007, 27 (43), 11587.
(67) Yoo, S.-W.; Motari, M. G.; Susuki, K.; Prendergast, J.; Mountney, A.; Hurtado, A.; Schnaar, R. L. Sialylation Regulates Brain Structure and Function. FASEB J.2015, 29 (7), 3040–3053.
(68) Pshezhetsky, A. V; Ashmarina, M. Keeping It Trim: Roles of Neuraminidases in CNS Function. Glycoconj. J.2018, 35 (4), 375.
(69) Kilcoyne, M.; Sharma, S.; McDevitt, N.; O’Leary, C.; Joshi, L.; McMahon, S. S. Neuronal Glycosylation Differentials in Normal, Injured and Chondroitinase-Treated Environments. Biochem. Biophys. Res. Commun.2012, 420 (3), 616.
(70) Zamze, S.; Harvey, D. J.; Chen, Y. J.; Guile, G. R.; Dwek, R. A.; Wing, D. R. Sialylated N-Glycans in Adult Rat Brain Tissue - A Widespread Distribution of Disialylated Antennae in Complex and Hybrid Structures. Eur. J. Biochem.1998, 258 (1), 243.
(71) Krusius, T.; Finne, J. Structural Features of Tissue Glycoproteins. Fractionation and Methylation Analysis of Glycopeptides Derived from Rat Brain, Kidney and Liver. Eur. J. Biochem.1977, 78 (2), 369.
(72) Cremer, H.; Chazal, G.; Goridis, C.; Represa, A. NCAM Is Essential for Axonal Growth and Fasciculation in the Hippocampus. Mol. Cell. Neurosci.1997, 8 (5), 323.
(73) Seki, T.; Arai, Y. Distribution and Possible Roles of the Highly Polysialylated Neural Cell Adhesion Molecule (NCAM-H) in the Developing and Adult Central Nervous System. Neurosci. Res.1993, 17 (4), 265.
(74) Nomura, T.; Yabe, T.; Rosenthal, E. S.; Krzan, M.; Schwartz, J. P. PSA‐NCAM Distinguishes Reactive Astrocytes in 6‐OHDA‐lesioned Substantia Nigra from Those in the Striatal Terminal Fields. J. Neurosci. Res.2000, 61, 588.
(75) Kiss, J. Z.; Wang, C.; Rougon, G. Nerve-Dependent Expression of High Polysialic Acid Neural Cell Adhesion Molecule in Neurohypophysial Astrocytes of Adult Rats. Neuroscience1993, 53 (1), 213.
(76) Shimizu, H.; Ochiai, K.; Ikenaka, K.; Mikoshiba, K.; Hase, S. Structures of N-Linked Sugar Chains Expressed Mainly in Mouse Brain. J. Biochem.1993, 114 (3), 334.
(77) Schneider, M.; Al-sharef, E.; Haltiwanger, R. S. Biological Functions of Fucose in Mammals. Glycobiology2017, 27 (7), 601.
(78) Fukuda, T.; Hashimoto, H.; Okayasu, N.; Kameyama, A.; Onogi, H.; Nakagawasai, O.; Nakazawa, T.; Kurosawa, T.; Hao, Y.; Isaji, T.; Tadano, T.; Narimatsu, H.; Taniguchi, N.; Gu, J. Alpha1,6-Fucosyltransferase-Deficient Mice Exhibit Multiple Behavioral Abnormalities Associated with a Schizophrenia-like Phenotype: Importance of the Balance between the Dopamine and Serotonin Systems. J. Biol. Chem.2011, 286 (21), 18434.
(79) Gu, W.; Fukuda, T.; Isaji, T.; Hang, Q.; Lee, H. H.; Sakai, S.; Morise, J.; Mitoma, J.; Higashi, H.; Taniguchi, N.; Yawo, H.; Oka, S.; Gu, J. Loss of Α1,6-Fucosyltransferase Decreases Hippocampal Long Term Potentiation: Implications for Core Fucosylation in the Regulation of AMPA Receptor Heteromerization and Cellular Signaling. J. Biol. Chem.2015, 290 (28), 17566.
(80) Kalovidouris, S. A.; Gama, C. I.; Lee, L. W.; Hsieh-Wilson, L. C. A Role for Fucose Alpha(1-2)Galactose Carbohydrates in Neuronal Growth. J. Am. Chem. Soc.2005, 9 (127), 1340.
(81) Nishihara, S.; Iwasaki, H.; Nakajima, K.; Togayachi, A.; Ikehara, Y.; Kudo, T.; Kushi, Y.; Furuya, A.; Shitara, K.; Narimatsu, H. Alpha1,3-Fucosyltransferase IX (Fut9) Determines Lewis X Expression in Brain. Glycobiology2003, 13 (6), 445.
(82) Hennen, E.; Czopka, T.; Faissner, A. Structurally Distinct LewisX Glycans Distinguish Subpopulations of Neural Stem/Progenitor Cells. J. Biol. Chem.2011, 286 (18), 16321.
(83) Satoh, J.; Kim, S. U. Differential Expression of Lewisx and Sialyl-Lewisx Antigens in Fetal Human Neural Cells in Culture. J. Neurosci. Res.1994, 37 (4), 466.
(84) Kudo, T.; Fujii, T.; Ikegami, S.; Inokuchi, K.; Takayama, Y.; Ikehara, Y.; Nishihara, S.; Togayachi, A.; Takahashi, S.; Tachibana, K.; Yuasa, S.; Narimatsu, H. Mice Lacking Alpha1,3-Fucosyltransferase IX Demonstrate Disappearance of Lewis x Structure in Brain and Increased Anxiety-like Behaviors. Glycobiology2007, 17 (1), 1.
(85) Regnier-Vigouroux, A. The Mannose Receptor in the Brain. Int. Rev. Cytol.2003, 226, 321.
(86) Harvey, D. J. Negative Ion Mass Spectrometry for the Analysis of N-Linked Glycans. 2019, 39, 586.
(87) Holst, S.; Heijs, B.; De Haan, N.; Van Zeijl, R. J. M.; Briaire-De Bruijn, I. H.; Van Pelt, G. W.; Mehta, A. S.; Angel, P. M.; Mesker, W. E.; Tollenaar, R. A.; Drake, R. R.; Bovée, J. V. M. G.; McDonnell, L. A.; Wuhrer, M. Linkage-Specific in Situ Sialic Acid Derivatization for N-Glycan Mass Spectrometry Imaging of Formalin-Fixed Paraffin-Embedded Tissues. Anal. Chem.2016, 88 (11), 5904
(88) Eshghi, S. T.; Yang, S.; Wang, X.; Shah, P.; Li, X.; Zhang, H. Imaging of N-Linked Glycans from Formalin-Fixed Paraffin-Embedded Tissue Sections Using MALDI Mass Spectrometry. ACS Chem. Biol.2014, 9 (9), 2149.