Expression of intercellular adhesion molecule 1 (ICAM-1) in Alzheimer’s disease
Abstract
In this study, 13 clinically and pathologically diagnosed cases of Alzheimer's disease were analyzed for the presence of intercellular adhesion molecule 1 (ICAM-1), ICAM-2, lymphocyte function associated antigen-1 (LFA-1), HLA-DR, LN-1, and LN-2. ICAM-1 was observed primarily on neuritic plaques and cerebrovascular endothelium. ICAM-1 was also shown to be present in brain tissue derived from 14 normal cases; however, the degree of immunoreactivity was quantitatively less compared to Alzheimer cases and was largely restricted to cerebrovascular endothelium. LFA-1 was shown to be present on microglial cells and leukocytes. Consistent with the findings of previous reports, HLA-DR was found to be expressed on microglial cells. In this study we failed to demonstrate dual immunolocalization for ICAM-1 and LFA-1, ICAM-1 and HLA-DR, or ICAM-1 and LN-2. As microglial cells express both HLA-DR and LFA-1, they may serve to mediate antigen presentation functions by interacting with lymphocyte ICAM-1. Alternately, the expression of these immune-associated glycoproteins on glial cells may be epiphenomenal occurring secondary to some aspect of the disease process. Finally, the presence of ICAM-1 within neuritic plaques raises the question as to whether adhesion may play some role in the process of neurite outgrowth and neurodegeneration.
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ICAM-1 is highly expressed in endothelial cells of AD patients.
“However, the intercellular adhesion molecule-1 (ICAM-1) was shown to be highly expressed in endothelial cells of AD patients.486”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [486]
ICAM-1, a biomarker of endothelial dysfunction, is increased in Alzheimer's disease, and endothelial cells, astrocytes and microglia show enhanced levels of ICAM-1 in pathological states.
“Experimental evidence confirmed that biomarkers of endothelial dysfunction, such as intercellular adhesion molecule 1 (ICAM-1), are increased in AD; endothelial cells, astrocytes and microglia show enhanced levels of ICAM-1 in pathological states”
From Beneficial Effects of Spirulina Consumption on Brain Health (2022) · cites this paper as [146]
ICAM-1 plays a role in neuritic plaques on neurite growth and neurodegeneration.
“and this plays a role in neuritic plaques on neurite growth and neurodegeneration [145,146,147].”
From Beneficial Effects of Spirulina Consumption on Brain Health (2022) · cites this paper as [146]
Cites
New Perspectives in Cell Adhesion: RGD and Integrins
Ruoslahti, E. I., & Pierschbacher, M. D. (1987) · Science · doi:10.1126/science.2821619 · Cited by 4,893 · see citing works
McGeer, P. L., Itagaki, S., Boyes, B. E., & McGeer, E. G. (1988) · Neurology · doi:10.1212/wnl.38.8.1285 · Cited by 2,990 · see citing works
Dustin, M. L., Rothlein, R., Bhan, A. K., Dinarello, C. A., & Springer, T. A. (1986) · The Journal of Immunology · doi:10.4049/jimmunol.137.1.245 · Cited by 2,450 · see citing works
A human intercellular adhesion molecule (ICAM-1) distinct from LFA-1.
Rothlein, R., Dustin, M. L., Marlin, S. D., & Springer, T. A. (1986) · The Journal of Immunology · doi:10.4049/jimmunol.137.4.1270 · Cited by 1,400 · see citing works
Rogers, J., Luber-Narod, J., Styren, S. D., & Civin, W. H. (1988) · Neurobiology of Aging · doi:10.1016/s0197-4580(88)80079-4 · Cited by 743 · see citing works
ICAM, an adhesion ligand of LFA-1, is homologous to the neural cell adhesion molecule NCAM
Simmons, D., Makgoba, M. W., & Seed, B. (1988) · Nature · doi:10.1038/331624a0 · Cited by 630 · see citing works
Griffiths, C. E. M., Voorhees, J. J., & Nickoloff, B. J. (1989) · Journal of the American Academy of Dermatology · doi:10.1016/s0190-9622(89)70073-6 · Cited by 503 · see citing works
Antigen presentation: comments on its regulation and mechanism.
Unanue, E. R., Beller, D. I., Lu, C., & Allen, P. M. (1984) · The Journal of Immunology · doi:10.4049/jimmunol.132.1.1 · Cited by 497 · see citing works
Brain microglia constitutively express β-2 integrins
Akiyama, H., & McGeer, P. L. (1990) · Journal of Neuroimmunology · doi:10.1016/0165-5728(90)90055-r · Cited by 430 · see citing works
Expression of the histocompatibility glycoprotein HLA-DR in neurological disease
McGeer, P. L., Itagaki, S., & McGeer, E. G. (1988) · Acta Neuropathologica · doi:10.1007/bf00689592 · Cited by 420 · see citing works
Dougherty, G. J., Murdoch, S., & Hogg, N. (1988) · European Journal of Immunology · doi:10.1002/eji.1830180107 · Cited by 346 · see citing works
Itagaki, S., McGeer, P. L., & Akiyama, H. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90690-8 · Cited by 271 · see citing works
Frohman, E. M., Frohman, T. C., Dustin, M. L., Vayuvegula, B., Choi, B. H., Gupta, A. A., van den Noort, S., & Gupta, S. (1989) · Journal of Neuroimmunology · doi:10.1016/0165-5728(89)90030-1 · Cited by 219 · see citing works
Rozemüller, A. J. M., Eikelenboom, P., Pals, S. T., & Stam, F. C. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90547-8 · Cited by 173 · see citing works
Understanding the molecules of neural cell contacts: emerging patterns of structure and function
Lander, A. D. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90070-2 · Cited by 112 · see citing works
Tumor necrosis factor amplifies measles virus-mediated Ia induction on astrocytes.
Massa, P. T., Schimpl, A., Wecker, E., & ter Meulen, V. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.20.7242 · Cited by 105 · see citing works
The role of monocyte lymphocyte function‐associated antigen 1 (LFA‐1) in accessory cell function
Dougherty, G. J., & Hogg, N. (1987) · European Journal of Immunology · doi:10.1002/eji.1830170708 · Cited by 77 · see citing works
Flagged first, then by citations
1 of the 18 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Role of neuroinflammation in neurodegeneration development
Zhang, W., Xiao, D., Mao, Q., & Xia, H. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01486-5 · Cited by 1,668 · see citing works
“However, the intercellular adhesion molecule-1 (ICAM-1) was shown to be highly expressed in endothelial cells of AD patients.(486) In vitro stimulating of human brain endothelial cells with Aβ or TNF-α induced the expression of endothelial adhesion molecules, including selectin, ICAM-1, and vascular cell adhesion prot…”
BackgroundMCGEER, P., & MCGEER, E. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(95)00011-9 · Cited by 1,287 · see citing works
The blood-brain barrier in Alzheimer’s disease
Zenaro, E., Piacentino, G., & Constantin, G. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.07.007 · Cited by 767 · see citing works
Neuroinflammation Induces Neurodegeneration.
Kempuraj, D., Thangavel, R., Natteru, P., Selvakumar, G. P., Saeed, D., Zahoor, H., Zaheer, S., Iyer, S. S., & Zaheer, A. (2016) · PubMed · Cited by 672 · see citing works
Microglia in degenerative neurological disease
McGeer, P. L., Kawamata, T., Walker, D. G., Akiyama, H., Tooyama, I., & McGeer, E. G. (1993) · Glia · doi:10.1002/glia.440070114 · Cited by 500 · see citing works
Inflammation and Alzheimer's disease pathogenesis
Rogers, J., Webster, S. D., Lue, L., Brachova, L., CIVIN, W. H., Emmerling, M. R., Shivers, B. D., Walker, D. G., & McGeer, P. L. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00115-7 · Cited by 441 · see citing works
Grammas, P. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-26 · Cited by 432 · see citing works
Selective expression of adhesion molecules on human brain microvascular endothelial cells
Stins, M. F., Gilles, F. H., & Kim, K. S. (1997) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(97)00036-2 · Cited by 365 · see citing works
Tarkowski, E., Issa, R., Sjögren, M., Wallin, A., Blennow, K., Tarkowski, A., & Kumar, P. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00285-8 · Cited by 360 · see citing works
Blood–Brain Barrier Pathology in Alzheimer's and Parkinson's Disease: Implications for Drug Therapy
Desai, B. S., Monahan, A. J., Carvey, P. M., & Hendey, B. (2007) · Cell Transplantation · doi:10.3727/000000007783464731 · Cited by 339 · see citing works
Inflammatory factors are elevated in brain microvessels in Alzheimer's disease
Grammas, P. (2001) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00276-7 · Cited by 292 · see citing works
Marco, L. Y. D., Venneri, A., Farkas, E., Evans, P. C., Marzo, A., & Frangi, A. F. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.08.014 · Cited by 258 · see citing works
The role of complement and activated microglia in the pathogenesis of Alzheimer's disease
Eikelenboom, P., & Veerhuis, R. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00108-x · Cited by 206 · see citing works
The Blood‐Brain Barrier and Cerebrovascular Pathology in Alzheimer's Disease
Kalaria, R. N. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb07821.x · Cited by 194 · see citing works
Arendt, T. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.09.007 · Cited by 188 · see citing works
Identification of oxidized plasma proteins in Alzheimer's disease
Choi, J., Malakowsky, C. A., Talent, J. M., Conrad, C. C., & Gracy, R. W. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)00420-5 · Cited by 183 · see citing works
Devassy, J. G., Leng, S., Gabbs, M., Monirujjaman, M., & Aukema, H. M. (2016) · Advances in Nutrition · doi:10.3945/an.116.012187 · Cited by 184 · see citing works
Tau Protein and Its Role in Blood–Brain Barrier Dysfunction
Michalicová, A., Majerová, P., & Kováč, A. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.570045 · Cited by 179 · see citing works
Xu, F.-L., Piett, C., Farkas, S., Qazzaz, M., & Syed, N. (2013) · Molecular Brain · doi:10.1186/1756-6606-6-29 · Cited by 176 · see citing works
Rossi, B., Angiari, S., Zenaro, E., Budui, S. L., & Constantin, G. (2010) · Journal of Leukocyte Biology · doi:10.1189/jlb.0710432 · Cited by 169 · see citing works
Alzheimer's disease as a disorder of mechanisms underlying structural brain self-organization
Arendt, T. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00516-9 · Cited by 168 · see citing works
Kamat, P. K., Kyles, P., Kalani, A., & Tyagi, N. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9212-4 · Cited by 163 · see citing works
Roher, A. E., Palmer, K. C., Yurewicz, E. C., Ball, M. J., & Greenberg, B. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb09834.x · Cited by 147 · see citing works
α-Synuclein Expression Modulates Microglial Activation Phenotype
Austin, S. A., Floden, A. M., Murphy, E. J., & Combs, C. K. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1799-06.2006 · Cited by 142 · see citing works
Akiyama, H., Kawamata, T., Yamada, T., Tooyama, I., Ishii, T., & McGeer, P. L. (1993) · Acta Neuropathologica · doi:10.1007/bf00334673 · Cited by 137 · see citing works
Structure and function of amyloid in Alzheimer's disease
Morgan, C., Colombres, M., Núñez, M. T., & Inestrosa, N. C. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.10.004 · Cited by 136 · see citing works
Fard, M. T., & Stough, C. K. K. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00056 · Cited by 121 · see citing works
An Integrated View on Vascular Dysfunction in Alzheimer’s Disease
Klohs, J. (2019) · Neurodegenerative Diseases · doi:10.1159/000505625 · Cited by 111 · see citing works
Blood–Brain Barrier Penetrating Biologic TNF-α Inhibitor for Alzheimer’s Disease
Chang, R., Knox, J., Chang, J. H., Derbedrossian, A., Vasilevko, V., Cribbs, D. H., Boado, R. J., Pardridge, W. M., & Sumbria, R. K. (2017) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.7b00200 · Cited by 113 · see citing works
Grace, E. A., & Busciglio, J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00493.2003 · Cited by 113 · see citing works
Death by a Thousand Cuts in Alzheimer’s Disease: Hypoxia—The Prodrome
Daulatzai, M. A. (2013) · Neurotoxicity Research · doi:10.1007/s12640-013-9379-2 · Cited by 111 · see citing works
(1994) · PubMed Central · Cited by 105 · see citing works
Cotman, C. W., Hailer, N. P., Pfister, K. K., Soltész, I., & Schachner, M. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00025-2 · Cited by 101 · see citing works
Beneficial Effects of Spirulina Consumption on Brain Health
Trotta, T., Porro, C., Cianciulli, A., & Panaro, M. A. (2022) · Nutrients · doi:10.3390/nu14030676 · Cited by 98 · see citing works
Intersection between metabolic dysfunction, high fat diet consumption, and brain aging
Uranga, R. M., Bruce‐Keller, A. J., Morrison, C. D., Fernandez‐Kim, S. O., Ebenezer, P. J., Zhang, L., Dasuri, K., & Keller, J. N. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06803.x · Cited by 87 · see citing works
Carvalho, C., Machado, N. J., Mota, P. C., Correia, S. C., Cardoso, S., Santos, R. X., Santos, M. S., Oliveira, C. R., & Moreira, P. I. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-130005 · Cited by 85 · see citing works
Jeong, E.-M., Moon, C., Kim, C., Lee, S., Baik, E. J., Moon, C.-K., & Jung, Y. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.05.218 · Cited by 84 · see citing works
Soluble adhesion molecules and angiotensin-converting enzyme in dementia
Nielsen, H. M., Londos, E., Minthon, L., & Janciauskiene, S. M. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.11.011 · Cited by 80 · see citing works
Imaging of cerebrovascular pathology in animal models of Alzheimer's disease
Klohs, J., Rudin, M., Shimshek, D. R., & Beckmann, N. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00032 · Cited by 82 · see citing works
A damaged microcirculation contributes to neuronal cell death in Alzheimer’s disease☆
Grammas, P. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00102-0 · Cited by 81 · see citing works
Molecular Basis of Etiological Implications in Alzheimer’s Disease: Focus on Neuroinflammation
Niranjan, R. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8428-4 · Cited by 81 · see citing works
Amyloid beta acts synergistically as a pro-inflammatory cytokine
LaRocca, T. J., Cavalier, A. N., Roberts, C. M., Lemieux, M. R., Ramesh, P., Garcia, M. A., & Link, C. D. (2021) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105493 · Cited by 76 · see citing works
Eikelenboom, P., Zhan, S., Kamphorst, W., van der Valk, P., & Rozemüller, A. J. M. (1994) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/bf00190565 · Cited by 78 · see citing works
Prasad, K. N., Cole, W. C., & Prasad, K. C. (2002) · Journal of the American College of Nutrition · doi:10.1080/07315724.2002.10719249 · Cited by 76 · see citing works
Hailer, N. P., Bechmann, I., Heizmann, S., & Nitsch, R. (1997) · Hippocampus · doi:10.1002/(sici)1098-1063(1997)7:3 · Cited by 77 · see citing works
Prasad, K. N., Hovland, A. R., Cole, W. C., Prasad, K. C., Nahreini, P., Edwards‐Prasad, J., & Andreatta, C. P. (2000) · Clinical Neuropharmacology · doi:10.1097/00002826-200001000-00002 · Cited by 74 · see citing works
Apelin, a promising target for Alzheimer disease prevention and treatment
Masoumi, J., Abbasloui, M., Parvan, R., Mohammadnejad, D., Pavon‐Djavid, G., Barzegari, A., & Abdolalizadeh, J. (2018) · Neuropeptides · doi:10.1016/j.npep.2018.05.008 · Cited by 69 · see citing works
Microglial interaction with β‐amyloid: Implications for the pathogenesis of Alzheimer's disease
Bamberger, M. E., & Landreth, G. E. (2001) · Microscopy Research and Technique · doi:10.1002/jemt.1121 · Cited by 71 · see citing works
Bell, M. D., & Perry, V. H. (1995) · Journal of Neurocytology · doi:10.1007/bf01179819 · Cited by 70 · see citing works
The Immunopathology of Alzheimer's Disease and Some Related Disorders
Kalaria, R. N. (1993) · Brain Pathology · doi:10.1111/j.1750-3639.1993.tb00761.x · Cited by 69 · see citing works
Anti-Selectin Therapy for the Treatment of Inflammatory Diseases
Rossi, B., & Constantin, G. (2008) · Inflammation & Allergy - Drug Targets · doi:10.2174/187152808785107633 · Cited by 66 · see citing works
Cell adhesion molecules in Alzheimer's disease
Nielsen, H. M., & Wennström, M. (2012) · Degenerative Neurological and Neuromuscular Disease · doi:10.2147/dnnd.s19829 · Cited by 64 · see citing works
Expression of CAP37, a Novel Inflammatory Mediator, in Alzheimer's Disease
Pereira, H. A., Kumar, P., & Grammas, P. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00118-2 · Cited by 62 · see citing works
Expression of CAP37, a Novel Inflammatory Mediator, in Alzheimer's Disease
Pereira, H. (1996) · Neurobiology of Aging · doi:10.1016/s0197-4580(96)00118-2 · Cited by 62 · see citing works
Hassan, M., Raza, H., Abbasi, M. A., Moustafa, A. A., & Seo, S. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.11.115 · Cited by 61 · see citing works
Relationship between Inflammatory Mediators, A? Levels and ApoE Genotype in Alzheimer Disease
Reale, M., Kamal, M. A., Velluto, L., Gambi, D., Nicola, M. D., & Greig, N. H. (2012) · Current Alzheimer Research · doi:10.2174/156720512800492549 · Cited by 51 · see citing works
Dimopoulos, N. P., Piperi, C., Salonicioti, A., Mitropoulos, P., Kallai, E., Liappas, I., Lea, R. W., & Kalofoutis, A. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2005.12.064 · Cited by 51 · see citing works
Rentzos, M., Michalopoulou, M., Nikolaou, C., Cambouri, C., Rombos, A., Dimitrakopoulos, A., Kapaki, E., & Vassilopoulos, D. (2004) · Journal of Geriatric Psychiatry and Neurology · doi:10.1177/0891988704269822 · Cited by 50 · see citing works
The role of soluble intercellular adhesion molecules in neurodegenerative disorders
Rentzos, M., Michalopoulou, M., Nikolaou, C., Cambouri, C., Rombos, A., Dimitrakopoulos, A., & Vassilopoulos, D. (2005) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2004.11.001 · Cited by 45 · see citing works
Biomarkers Assessing Endothelial Dysfunction in Alzheimer’s Disease
Custodia, A., Aramburu-Núñez, M., Rodríguez‐Arrizabalaga, M., Peleteiro, J. M. P., Vázquez‐Vázquez, L., Camino-Castiñeiras, J., Aldrey, J. M., Castillo, J., Ouro, A., Sobrino, T., et al. (2023) · Cells · doi:10.3390/cells12060962 · Cited by 44 · see citing works
Activation of microglia: A neuroinflammatory role for CAP37
Pereira, H., Ruan, X.-J., & Kumar, P. (2003) · Glia · doi:10.1002/glia.10167 · Cited by 42 · see citing works
Solerte, S. B., Ferrari, E., Cuzzoni, G., Locatelli, E., Giustina, A., Zamboni, M. M., Schifino, N., Rondanelli, M., Gazzaruso, C., & Fioravanti, M. (2004) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000080963 · Cited by 41 · see citing works
Thrombin, a Key Driver of Pathological Inflammation in the Brain
Iannucci, J., & Grammas, P. (2023) · Cells · doi:10.3390/cells12091222 · Cited by 38 · see citing works
Nutraceutical and therapeutic potential of Phycocyanobilin for treating Alzheimer’s disease
Piniella‐Matamoros, B., Marín‐Prida, J., & Pentón‐Rol, G. (2021) · Journal of Biosciences · doi:10.1007/s12038-021-00161-7 · Cited by 34 · see citing works
Distribution of ICAM-1 immunoreactivity during aging in the human orbitofrontal cortex
Miguel-Hidalgo, J. J., Nithuairisg, S., Stockmeier, C. A., & Rajkowska, G. (2006) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2006.05.001 · Cited by 33 · see citing works
Walker, D. G., Lue, L.-F., Tang, T. M., Adler, C. H., Caviness, J. N., Sabbagh, M. N., Serrano, G. E., Sue, L. I., & Beach, T. G. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.03.007 · Cited by 33 · see citing works
The vascular contribution to cognitive decline in ageing and dementia
Anderle, S., Dixon, M., Quintela‐López, T., Sideris-Lampretsas, G., & Attwell, D. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00950-1 · Cited by 38 · see citing works
Intercellular adhesion molecule-1 K469E gene polymorphism and Alzheimer’s disease
Pola, R., Flex, A., Gaetani, E., Santoliquido, A., Serricchio, M., Pola, P., & Bernabei, R. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00087-8 · Cited by 32 · see citing works
Interactions between nanoparticles and pathological changes of vascular in Alzheimer’s disease
Lei, T., Yang, Z., Li, H., Qin, M., & Gao, H. (2024) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2024.115219 · Cited by 32 · see citing works
Iannucci, J., Rao, H. V., & Grammas, P. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00987-z · Cited by 32 · see citing works
Unusual aspects of inflammation in the nervous system: Wallerian degeneration
Castaño, A., Bell, M. D., & Perry, V. H. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00105-4 · Cited by 31 · see citing works
Macdonald, D. W., Berdoy, M., & Webster, J. P. (2015) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198745501.003.0011 · Cited by 27 · see citing works
Neuroimmune nexus of depression and dementia: Shared mechanisms and therapeutic targets
Herman, F. J., Simkovic, S. J., & Pasinetti, G. M. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14569 · Cited by 29 · see citing works
Male, D. K., & Rezaie, P. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)32067-8 · Cited by 26 · see citing works
Wang, Z., Tang, X., Swaminathan, S. K., Kandimalla, K. K., & Kalari, K. R. (2022) · npj Systems Biology and Applications · doi:10.1038/s41540-022-00235-8 · Cited by 24 · see citing works
Miller, M. R., Landis, H. E., Miller, R. E., & Tizabi, Y. (2024) · Cells · doi:10.3390/cells13181554 · Cited by 24 · see citing works
Inhibition of Early Upstream Events in Prodromal Alzheimer’s Disease by Use of Targeted Antioxidants
Prasad, K. N., & Bondy, S. C. (2014) · Current Aging Science · doi:10.2174/1874609807666140804115633 · Cited by 24 · see citing works
Ritson, M., Wheeler-Jones, C. P. D., & Stolp, H. B. (2024) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2024.578363 · Cited by 23 · see citing works
sPDGFRβ and neuroinflammation are associated with AD biomarkers and differ by race: The ASCEND Study
Butts, B., Huang, H., Hu, W. T., Kehoe, P. G., Miners, J. S., Verble, D. D., Zetterberg, H., Zhao, L., Trotti, L. M., Benameur, K., et al. (2023) · Alzheimer s & Dementia · doi:10.1002/alz.13457 · Cited by 20 · see citing works
Apelt, J., Leßig, J., & Schliebs, R. (2002) · Neuroscience Letters · doi:10.1016/s0304-3940(02)00589-x · Cited by 21 · see citing works
Inflammatory Mediators in Alzheimer’s Disease
Rogers, J., & O’Barr, S. A. (1997) · Humana Press eBooks · doi:10.1007/978-1-59259-471-9_11 · Cited by 21 · see citing works
Gunawan, C., Fleming, C. L., Irga, P. J., Wong, R. J., Amal, R., Torpy, F. R., Golzan, M., & McGrath, K. C. Y. (2024) · Environment International · doi:10.1016/j.envint.2024.108512 · Cited by 20 · see citing works
Hanson, A. J., Prasad, J. E., Nahreini, P., Andreatta, C. P., Kumar, B., Yan, X., & Prasad, K. N. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10726 · Cited by 20 · see citing works
Inflammation in Alzheimer's disease: a view from the periphery
Raine, C. S. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00138-x · Cited by 20 · see citing works
Production of Neurotoxic Factors by Brain Endothelium in Alzheimer's Diseasea
Grammas, P., Botchlet, T., Moore, P., & Weigel, P. H. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb48460.x · Cited by 19 · see citing works
A link between sICAM-1, ACE and parietal blood flow in the aging brain
Janciauskiene, S. M., Erikson, C. A., & Warkentin, S. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.08.025 · Cited by 18 · see citing works
Wu, C., Peng, P., Renn, T., Lee, C., Chang, T., Wei, A. I., & Liu, J. (2023) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17750 · Cited by 17 · see citing works
Kwak, M., Kim, D., Lee, M.-R., Wu, Y., Han, L. G., Lee, S., & Fan, R. (2014) · Nanoscale · doi:10.1039/c3nr06465d · Cited by 16 · see citing works
Cerebrovasculature‐mediated Neuronal Cell Death
Grammas, P., Reimann‐Philipp, U., & Weigel, P. H. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06350.x · Cited by 16 · see citing works
Role of hydrogen sulfide in cerebrovascular alteration during aging
Mun, J., Kang, H.-M., Jung, J., & Park, C. (2019) · Archives of Pharmacal Research · doi:10.1007/s12272-019-01135-y · Cited by 15 · see citing works
Do Nonsteroidal Anti-Inflammatory Drugs Have a Protective Effect Against Dementia?
Muiswinkel, F. L. V., & Eikelenboom, P. (1996) · Drugs & Aging · doi:10.2165/00002512-199609010-00001 · Cited by 15 · see citing works
Roles of CNS Macrophages in Neurodegeneration
Wood, P. L. (1998) · Humana Press eBooks · doi:10.1007/978-1-59259-473-3_1 · Cited by 14 · see citing works
Inflammatory Mechanisms of Alzheimer’s Disease
Rogers, J., & Griffin, W. S. T. (1998) · Humana Press eBooks · doi:10.1007/978-1-59259-473-3_6 · Cited by 14 · see citing works
Inhibition of Monocyte Adhesion to Brain-Derived Endothelial Cells by Dual Functional RNA Chimeras
Hu, J., Xiao, F., Hao, X., Bai, S., & Hao, J. (2014) · Molecular Therapy — Nucleic Acids · doi:10.1038/mtna.2014.60 · Cited by 13 · see citing works
T-Cell Interferon Gamma Binding in Patients With Dementia of the Alzheimer Type
Bongioanni, P., Boccardi, B., Borgna, M., Castagna, M., & Mondino, C. (1997) · Archives of Neurology · doi:10.1001/archneur.1997.00550160085021 · Cited by 13 · see citing works
Park, J., Kim, H., & Han, H.-J. (2008) · Neurological Sciences · doi:10.1007/s10072-008-0996-0 · Cited by 12 · see citing works
Inflammaging: inflammation and oxidative stress as a cause of aging and cognitive decline
Pereverzev, A. P., Romanovsky, R. R., Shatalova, N. A., & Ostroumova, O. D. (2021) · Meditsinskiy sovet = Medical Council · doi:10.21518/2079-701x-2021-4-48-58 · Cited by 11 · see citing works
Weng, W., Fu, J., Fan, C., Wang, Y., & Zhang, J. (2024) · Molecular Neurobiology · doi:10.1007/s12035-023-03907-6 · Cited by 6 · see citing works
Investigating the Relationship between Diabetes and Alzheimer’s Disease:
Sahrawat, T. R., & Dwivedi, J. (2020) · Journal of Science and Sustainable Development · doi:10.4314/jssd.v7i1.1 · Cited by 6 · see citing works
Myserlis, E. P., Ray, A., Anderson, C. D., & Georgakis, M. K. (2024) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1002/trc2.70000 · Cited by 5 · see citing works
- Authors
- Frohman, E. M., Frohman, T. C., Gupta, S., de Fougerolles, A., & van den Noort, S.
- Affiliations
- University of California, Irvine (US)
- Corresponding author
- Frohman, Elliot M.
- Venue
- Journal of the Neurological Sciences
- Publisher
- Elsevier BV
- Published
- 1991-11
- Volume
- 106
- Issue
- 1
- Pages
- 105-111
- ISSN
- 0022-510X (ISSN-L)
- OpenAlex
- W1968283018
- Cited by
- 120
- References
- 18
- Citations by year
- 2025: 2 · 2024: 6 · 2023: 5 · 2022: 2 · 2021: 4 · 2020: 4 · 2019: 6 · 2018: 2 · 2017: 3 · 2016: 3 · 2015: 3 · 2014: 4 · 2013: 4 · 2012: 3
- FWCI
- 1.64
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of the Neurological Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (AG 00538)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- ICAM-1, Alzheimer's disease, ICAM-2, LFA-1, HLA-DR, neuritic plaques, cerebrovascular endothelium, microglial cells, leukocytes, antigen presentation, glial cells, neurodegeneration, neurite outgrowth
- MeSH terms
- Alzheimer Disease, Cerebral Arteries, Endothelium, Vascular, HLA-DR Antigens, Humans, Macrophages, Nerve Tissue Proteins, Neuroglia, Biomarkers, Antigens, CD, Cell Adhesion Molecules, Lymphocyte Function-Associated Antigen-1, Intercellular Adhesion Molecule-1
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