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Astrocyte-like glia in the peripheral nervous system: an immunohistochemical study of enteric glia
Open accessAbstract
The similarities between the enteric nervous system of the gut and the central nervous system (CNS), both of which function as complex integrative nervous networks, include striking ultrastructural similarities between the glia of the enteric nervous system and the astrocytic glia of the CNS. In this paper we have determined whether this anatomical resemblance also extends to the molecular level by examining the enteric glial cells to see whether they express several surface and intracellular molecules which are highly restricted to glia and to astrocytes in particular. Indirect immunofluorescence was used to visualize the antigens in frozen sections of gut wall and in whole mount, tissue culture, and freshly dissected preparations of myenteric and submucous plexuses from rats of various ages. It was found that enteric glial cells expressed the intracellular proteins glial fibrillary acidic protein, glutamine synthetase, and vimentin both in situ and in culture. The surface antigen Ran-2 was expressed in situ but not in culture, and the surface antigen Ran-1 was expressed in culture but not in situ. Cultured enteric glial cells did not express fibronectin in significant quantity, nor did they make galactocerebroside. From these results we conclude that the adult phenotype of enteric glia in situ closely resembles that of astrocytes, while in culture some of their cell surface features change, reverting to those seen during development. Because these cells possess distinctive molecular features and numerically form one of the major populations of peripheral glia, it is appropriate to classify them as a third distinctive category of peripheral glial cells, in addition to satellite and Schwann cells. The molecular similarities between these cells and astrocytes, in addition to their anatomical resemblance, suggest that a further study of enteric glia will provide new insights into the role of glia in integrative nervous tissues.
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“It has been shown that enteric ganglia share some morphological similarities to CNS astrocytes (Jessen and Mirsky, 1983), which lie adjacent to enteric neuronal cell bodies, which are very much like glia in the CNS (Yoo and Mazmanian, 2017).”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Jessen and Mirsky, 1983
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Cites
DISTRIBUTION OF FIBROBLAST SURFACE ANTIGEN
Wartiovaara, J., Linder, E., Ruoslahti, E. I., & Vaheri, A. I. (1974) · The Journal of Experimental Medicine · doi:10.1084/jem.140.6.1522 · Cited by 165
Cited by
Sorted by citations
Items 101–200 of 246
Microbial Endocrinology in the Pathogenesis of Infectious Disease
Lyte, M. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.vmbf-0021-2015 · Cited by 44
Murakami, S., Miyazaki, I., Sogawa, N., Miyoshi, K., & Asanuma, M. (2014) · Neurotoxicity Research · doi:10.1007/s12640-014-9480-1 · Cited by 40
Electrophysiologic and molecular properties of cultured enteric glia
Broussardy, D. L., Bannerman, P. G. C., Tang, C., Hardy, M., & Pleasure, D. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490340104 · Cited by 42
The Physiology of Enteric Glia
Gonzales, J. A., & Gulbransen, B. D. (2024) · Annual Review of Physiology · doi:10.1146/annurev-physiol-022724-105016 · Cited by 46
Type I collagen preparations inhibit DNA synthesis in glial cells of the peripheral nervous system
Eccleston, P. A., Mirsky, R., & Jessen, K. R. (1989) · Experimental Cell Research · doi:10.1016/0014-4827(89)90289-9 · Cited by 39
Self-citationThe University of North Carolina at Chapel Hill University Libraries (2020) · PubMed Central · doi:10.17615/t123-hm09 · Cited by 39
Ammonia modifies enteric neuromuscular transmission through glial γ-aminobutyric acid signaling
Fried, D. E., Watson, R. E., Robson, S. C., & Gulbransen, B. D. (2017) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00154.2017 · Cited by 38
Eccleston, P. A., Jessen, K. R., & Mirsky, R. (1987) · Developmental Biology · doi:10.1016/0012-1606(87)90493-3 · Cited by 37
Self-citationHajós, F., Kálmán, M., Zilles, K., Schleicher, A., & Sótonyi, P. (1990) · Glia · doi:10.1002/glia.440030410 · Cited by 37
Viale, G., Doglioni, C., Dell’Orto, P., Zanetti, G. M. R., Iuzzolino, P., Bontempini, L., & Coggi, G. (1988) · PubMed Central · Cited by 36
Aquaporin‐4 water channels in enteric neurons
Thi, M. M., Spray, D. C., & Menachem Hanani, A. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21496 · Cited by 35
Establishment and properties of separate cultures of enteric neurons and enteric glia
Bannerman, P. G. C., Mirsky, R., & Jessen, K. R. (1988) · Brain Research · doi:10.1016/0006-8993(88)91162-6 · Cited by 35
Self-citationWhat a gastrointestinal biopsy can tell us about Parkinson's disease?
Corbillé, A.-G., Clairembault, T., Coron, E., Leclair‐Visonneau, L., Preterre, C., Neunlist, M., & Derkinderen, P. (2016) · Neurogastroenterology & Motility · doi:10.1111/nmo.12797 · Cited by 34
Presence of functionally active protease‐activated receptors 1 and 2 in myenteric glia
Garrido, R., Segura, B. J., Zhang, W., & Mulholland, M. T. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.01119.x · Cited by 34
2 Vagal control of gastrointestinal function
Grundy, D. (1988) · Baillière s Clinical Gastroenterology · doi:10.1016/0950-3528(88)90019-x · Cited by 34
Enteric glial reactivity to systemic LPS administration: Changes in GFAP and S100B protein
Franceschi, R. D. C., Nardin, P., Machado, C. V., Tortorelli, L. S., Martinez‐Pereira, M. A., Zanotto, C., Gonçalves, C., & Zancan, D. M. (2017) · Neuroscience Research · doi:10.1016/j.neures.2016.12.005 · Cited by 33
Protein kinase�C isoforms in the enteric nervous system
Poole, D. P., Hunne, B., Robbins, H. L., & Furness, J. B. (2003) · Histochemistry and Cell Biology · doi:10.1007/s00418-003-0541-4 · Cited by 33
Astrocytic pathology of methionine sulfoximine-induced encephalopathy
Yamamoto, T., Iwasaki, Y., Sato, Y., Yamamoto, H., & Konno, H. (1989) · Acta Neuropathologica · doi:10.1007/bf00687370 · Cited by 32
Recent Studies of the Glial Fibrillary Acidic Proteina
Eng, L. F., Smith, M. E., de Vellis, J., & Skoff, R. P. (1985) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1985.tb50433.x · Cited by 31
Gastrointestinal Motility in the Neonate
Broussard, D. L. (1995) · Clinics in Perinatology · doi:10.1016/s0095-5108(18)30300-2 · Cited by 30
Glial fibrillary acidic protein (GFAP)-like immunoreactivity in the rodent eye
Björklund, H., & Dahl, D. R. (1985) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(85)80071-0 · Cited by 30
Enteric Glial Cells in Immunological Disorders of the Gut
Liu, C., & Yang, J. H. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.895871 · Cited by 29
Enteric glia: Diversity or plasticity?
Valès, S., Touvron, M. S., & Landeghem, L. V. (2018) · Brain Research · doi:10.1016/j.brainres.2018.02.001 · Cited by 29
Enteric gliopathy in niacin-deficiency induced by CNS glio-toxin
Aikawa, H., & Suzuki, K. (1985) · Brain Research · doi:10.1016/0006-8993(85)90231-8 · Cited by 29
Murphy, M., Bernard, O., Reid, K., & Bartlett, P. F. (1991) · Journal of Neurobiology · doi:10.1002/neu.480220508 · Cited by 30
Palanisamy, B. N., Sarkar, S., Malovic, E., Samidurai, M., Charli, A., Zenitsky, G. D., Jin, H., Anantharam, V., Kanthasamy, A., & Kanthasamy, A. G. (2022) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2022.106225 · Cited by 29
Toma, H., Nakamura, K., Kuraoka, A., Tanaka, M., & Kawabuchi, M. (1999) · Cell and Tissue Research · doi:10.1007/s004410051249 · Cited by 28
The pathogenesis of proventricular dilatation disease
Tizard, I. R., Shivaprasad, H. L., Guo, J., Hameed, S. S., Ball, J. M., & Payne, S. (2016) · Animal Health Research Reviews · doi:10.1017/s1466252316000189 · Cited by 27
Glial cells revealed by GFAP immunoreactivity in fish gut
Hagström, C., & Olsson, C. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-0979-3 · Cited by 27
Kepes, J. J., & Perentes, E. (1988) · The Anatomical Record · doi:10.1002/ar.1092200311 · Cited by 27
Glutamatergic Functions of Primary Afferent Neurons with Special Emphasis on Vagal Afferents
Raab, M., & Neuhuber, W. (2007) · International review of cytology · doi:10.1016/s0074-7696(07)56007-9 · Cited by 27
Isolation, identification, and culture of normal mouse colonic glia
Bernstein, C. N., & Vidrich, A. (1994) · Glia · doi:10.1002/glia.440120204 · Cited by 27
Expression of bcl-2 in Enteric Neurons in Normal Human Bowel and Hirschsprung Disease
Wester, T., Olsson, Y., & Olsen, L. (1999) · Archives of Pathology & Laboratory Medicine · doi:10.5858/1999-123-1264-eobien · Cited by 26
Ganglia within the Gut, Heart, Urinary Bladder, and Airways: Studies in Tissue Culture
Saffrey, M. J., Hassall, C. J. S., Allen, T. G. J., & Burnstock, G. (1992) · International review of cytology · doi:10.1016/s0074-7696(08)62051-3 · Cited by 26
Mirsky, R., Gavrilović, J., Bannerman, P. G. C., Winter, J., & Jessen, K. R. (1985) · Cell and Tissue Research · doi:10.1007/bf00216361 · Cited by 26
Self-citationEnteric glia promote regeneration of transected dorsal root axons into spinal cord of adult rats
Jiang, S., Wang, J., Khan, M. I., Middlemiss, P. J., Salgado‐Ceballos, H., Werstiuk, E. S., Wickson, R., & Rathbone, M. P. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(02)00030-4 · Cited by 24
Enteric glia mediate neuronal outgrowth through release of neurotrophic factors.
Hansebout, C. R., Su, C., Reddy, K., Zhang, D., Jiang, C., Rathbone, M. P., & Jiang, S. (2012) · Europe PMC (PubMed Central) · doi:10.3969/j.issn.1673-5374.2012.028.001 · Cited by 23
Ajima, H., Kawano, Y., Takagi, R., Aita, M., Gomi, H., Byers, M. R., & Maeda, T. (2001) · Archivum histologicum japonicum · doi:10.1679/aohc.64.503 · Cited by 23
In Situ Ca2+ Imaging of the Enteric Nervous System
Fried, D. E., & Gulbransen, B. D. (2015) · Journal of Visualized Experiments · doi:10.3791/52506 · Cited by 23
Expression of aquaporin-4 water channels in the digestive tract of the guinea pig
Jiang, L., Li, J., Liu, X., Burnstock, G., & Xiang, Z. (2013) · Journal of Molecular Histology · doi:10.1007/s10735-013-9545-0 · Cited by 23
Jessen, K. R., & Mirsky, R. (2004) · Elsevier eBooks · doi:10.1016/b978-012439510-7/50066-8 · Cited by 23
Self-citationThe multiple roles of enteric glial cells in intestinal homeostasis and regeneration
Baghdadi, M. B., & Kim, T.-H. (2023) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2023.01.005 · Cited by 22
Morphology and Innervation of the Human Cremaster Muscle in Relation to its Function
Kayalıoğlu, G., Altay, B., Uyaroğlu, F. G., Bademkıran, F., Uludağ, B., & Erteki̇n, C. (2008) · The Anatomical Record · doi:10.1002/ar.20711 · Cited by 22
Bassotti, G., Macchioni, L., Corazzi, L., Marconi, P., & Fettucciari, K. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2736-1 · Cited by 22
Gulbransen, B. D. (2014) · Colloquium Series on Neuroglia in Biology and Medicine From Physiology to Disease · doi:10.4199/c00113ed1v01y201407ngl002 · Cited by 23
Neural Control of Gastrointestinal Function
Grundy, D., & Brookes, S. J. (2011) · Colloquium Series on Integrated Systems Physiology From Molecule to Function · doi:10.4199/c00048ed1v01y201111isp030 · Cited by 21
Suzuki, T., & Kachi, T. (1995) · PubMed · Cited by 21
Hirose, T., Ishizawa, K., Sakaki, M., & Fujii, Y. (2012) · Pathology International · doi:10.1111/j.1440-1827.2012.02822.x · Cited by 20
Schwann cells cultured from adult rats contain a cytoskeletal protein related to astrocyte filaments
Fields, K. L., & McMenamin, P. G. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90113-0 · Cited by 20
Antigenic markers and laminin expression in cultured enteric neural cells
Bannerman, P. G. C., Mirsky, R., & Jessen, K. R. (1988) · Brain Research · doi:10.1016/0006-8993(88)91161-4 · Cited by 19
Self-citationBehan, P. O., & Chaudhuri, A. (2010) · Inflammopharmacology · doi:10.1007/s10787-010-0054-4 · Cited by 18
The Biology of Non‐Myelin‐Forming Schwann Cellsa
Mirsky, R., & Jessen, K. R. (1986) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1986.tb48069.x · Cited by 18
Self-citationDahl, D. R., Zapatka, S. A., & Bignami, A. (1986) · Histochemistry and Cell Biology · doi:10.1007/bf00499825 · Cited by 17
Malcolm, L. A., Wright, L., Seers, M., Davies, L., & Guthrie, J. (2000) · PubMed · Cited by 17
López‐Gómez, L., Szymaszkiewicz, A., Zielińska, M., & Abalo, R. (2022) · Molecules · doi:10.3390/molecules27196773 · Cited by 16
Nutraceuticals and Enteric Glial Cells
López‐Gómez, L., Szymaszkiewicz, A., Zielińska, M., & Abalo, R. (2021) · Molecules · doi:10.3390/molecules26123762 · Cited by 16
Neuronal and Glial Surface Antigens on Cells in Culture
Fields, K. L. (1985) · Springer eBooks · doi:10.1007/978-1-4613-2473-7_2 · Cited by 16
Growth of myenteric plexus explant cultures in a serum‐free, hormone‐supplemented culture medium
Saffrey, M. J., & Burnstock, G. (1984) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(84)90037-6 · Cited by 16
Regulation of Pain Perception by Microbiota in Parkinson Disease
Manjarres, Z., Calvo, M., & Pacheco, R. (2023) · Pharmacological Reviews · doi:10.1124/pharmrev.122.000674 · Cited by 15
Roufa, D. G., Bunge, M., Johnson, M., & Cornbrooks, C. J. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-03-00790.1986 · Cited by 15
Enteric GliaPreprint
Rao, M., & Gulbransen, B. D. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041368 · Cited by 15
Cohen, G., Gover, O., & Schwartz, B. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914628 · Cited by 14
Giuliani, D., Giaroni, C., Zanetti, E., Canciani, L., Borroni, P., Lecchini, S., & Frigo, G. (2005) · Neurochemistry International · doi:10.1016/j.neuint.2005.10.005 · Cited by 14
Regulation of the early development of the nervous system by growth factors
Bartlett, P. F., Kilpatrick, T. J., Richards, L. J., Talman, P. S., & Murphy, M. (1994) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(94)00044-1 · Cited by 14
Yasuda, T., Sobue, G., Ito, T., Doyu, M., Sugiura, I., Hashizume, Y., & Kato, K. (1991) · Muscle & Nerve · doi:10.1002/mus.880140903 · Cited by 13
Li, B., Yang, Z., Hou, J., McCracken, A., Jennings, M. A., & Ma, M. Y. J. (2003) · Molecular Endocrinology · doi:10.1210/me.2003-0023 · Cited by 13
Potential roles of enteric glial cells in Crohn's disease: A critical review
Mao, X., & Shen, J. (2023) · Cell Proliferation · doi:10.1111/cpr.13536 · Cited by 10
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Reichenbach, A., & Bringmann, A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00050-6 · Cited by 12
LRRK2 expression in normal and pathologic human gut and in rodent enteric neural cell lines
de Lataillade, A. D. G., Caillaud, M., Oullier, T., Naveilhan, P., Pellegrini, C., TOLOSA, E. S., Neunlist, M., Rolli‐Derkinderen, M., Gelpí, E., & Derkinderen, P. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15704 · Cited by 12
Tachykinin signaling defines distinct populations of glia in the enteric nervous system
Muppirala, A. N., Mitchell, P. E., Courtney, E., Debnath, S., D’Alessandro, L. R., Mani, N., Dadabhoy, M., Robinson, A. F., Díaz-Muñoz, C., Paraskevopoulou, M. D., et al. (2026) · Neuron · doi:10.1016/j.neuron.2025.11.030 · Cited by 11
Pavone, S., Gialletti, R., Pepe, M., Onofri, A., & Mandara, M. T. (2011) · Research in Veterinary Science · doi:10.1016/j.rvsc.2011.07.019 · Cited by 11
Molecular Signaling in Schwann Cell Development
Mirsky, R., & Jessen, K. R. (2005) · Elsevier eBooks · doi:10.1016/b978-0-7216-9491-7.50019-3 · Cited by 11
Self-citationNeuroglia and the microbiota-gut-brain axis
Blair, H., Morales, L., Cryan, J. F., & Aburto, M. R. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00001-2 · Cited by 12
Shi, C., Lian, J.-J., Zhang, B.-W., Cha, J.-X., Hua, Q., Pi, X., Hou, Y., Xie, X., & Zhang, R. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-022-00932-4 · Cited by 10
Hansson, E., & Rönnbäck, L. (1985) · Journal of Neuroscience Research · doi:10.1002/jnr.490140409 · Cited by 10
Good, P. (2012) · Medical Hypotheses · doi:10.1016/j.mehy.2012.08.035 · Cited by 9
Glial fibrillary acidic protein (GFAP) immunoreactivity in enteric ganglia of the chick embryo
Balaskas, C., & Gabella, G. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00709-4 · Cited by 9
Patient-Specific Cell Communication Networks Associate With Disease Progression in Cancer
Gibbs, D. L., Aguilar, B. H., Thórsson, V., Ratushny, A. V., & Ilya Shmulevich, C. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.667382 · Cited by 8
Peripheral nerve fibres regenerate through myenteric plexus
Anderson, P. N., & Turmaine, M. (1987) · Neuroscience Letters · doi:10.1016/0304-3940(87)90703-8 · Cited by 8
Enteric glia regulate Paneth cell secretion and intestinal microbial ecology
Prochera, A., Muppirala, A. N., Kuziel, G. A., Soualhi, S., Shepherd, A., Sun, L., Issac, B., Rosenberg, H. J., Karim, F., Perez, K., et al. (2025) · eLife · doi:10.7554/elife.97144.3 · Cited by 7
Engineering the Niche for Intestinal Regeneration
Hernandez‐Gordillo, V., Koppes, A. N., Griffith, L. G., Breault, D. T., & Carrier, R. L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802734-9.00037-8 · Cited by 7
Neurons and Glial Cells of the Enteric Nervous System: Studies in Tissue Culture
Menachem Hanani, A. (1993) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp.1993.4.3.157 · Cited by 7
Heterogeneity and Potency of Peripheral Glial Cells in Embryonic Development and Adults
Sinegubov, A., Andreeva, D., Burzak, N., Vasyutina, M., Murashova, L. A., & Dyachuk, V. A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.737949 · Cited by 6
Zanoletti, L., Valdata, A., Nehlsen, K., Faris, P. S., Casali, C., Cacciatore, R., Sbarsi, I., Carriero, F., Arfini, D., van Baarle, L., et al. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1170309 · Cited by 6
Parra-Cid, C., García‐López, J., Garcı́a, E., & Ibarra, C. (2014) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2014.03.005 · Cited by 6
Enteric glia regulate Paneth cell secretion and intestinal microbial ecologyPreprint
Prochera, A., Muppirala, A. N., Kuziel, G. A., Soualhi, S., Shepherd, A., Sun, L., Issac, B., Rosenberg, H. J., Karim, F., Perez, K., et al. (2024) · eLife · doi:10.7554/elife.97144 · Cited by 6
Distribution and ultrastructural characteristics of enteric glial cell in the chicken cecum
Zhang, X., Qi, F., Yang, J., & Xu, C. (2024) · Poultry Science · doi:10.1016/j.psj.2024.104070 · Cited by 4
Immunohistochemical localization of aquaporin 4 (AQP4) in the porcine gastrointestinal tract
Arciszewski, M. B., Matysek, M., & Sienkiewicz, W. (2015) · Acta Veterinaria Brno · doi:10.2754/avb201584040321 · Cited by 4
Regulation of intestinal epithelial barrier by and dysfunction of intestinal glial cells
Di, Z.-S., Yang, Z., Zhu, M.-J., Wang, F., Li, L., & Xu, J. (2019) · World Chinese Journal of Digestology · doi:10.11569/wcjd.v27.i16.1013 · Cited by 4
Microbial Endocrinology in the Pathogenesis of Infectious Disease
Lyte, M. (2016) · ASM Press eBooks · doi:10.1128/9781555819286.ch6 · Cited by 4
Comparative Anatomy of Glial Cells in Mammals
Reichenbach, A., & Bringmann, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820584-6.00016-7 · Cited by 4
Coelho‐Aguiar, J. D. M., Veríssimo, C. P., Costa, D. V. D. S., Thomasi, B. B. D. M., Bon‐Frauches, A. C., Ribeiro, F. P., Gomes, A. L. T., Brito, G. A. D. C., & Moura‐Neto, V. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.89170 · Cited by 8
Morphological changes of the myenteric plexus at different gut segments of human fetuses
Bhukya, S., Singh, S., Sarwar, S., Quadri, J. A., Ahmed, A., Rani, N., Dheeraj, K., Dubey, A., Nag, T. C., & Shariff, A. (2021) · Journal of Histotechnology · doi:10.1080/01478885.2020.1862604 · Cited by 4
Willard, A. L., & Nishi, R. (1989) · Comprehensive physiology · doi:10.1002/cphy.cp060109 · Cited by 3
Variations in the cellular incorporation of [3H]proline
Contos, N., Molinari, H. H., & Berkley, K. J. (1989) · Brain Research · doi:10.1016/0006-8993(89)91349-8 · Cited by 3
Molecular Properties of Peripheral Glia
Mirsky, R., & Jessen, K. R. (1987) · Springer eBooks · doi:10.1007/978-3-642-71381-1_4 · Cited by 3
Self-citationDevelopment of the Enteric Nervous System
Broussard, D. L., & Altschuler, S. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-35214-7.00088-3 · Cited by 3
Morishita, R., Nakanishi, S., YOKOYAMA, T., Hoshi, N., & MANTANI, Y. (2025) · Cell and Tissue Research · doi:10.1007/s00441-025-03949-3 · Cited by 2
Astrocyte Marker GFAP in Gliocytes of Peripheral Nervous System
Petrova, E. S., & Kolos, E. A. (2024) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093024050090 · Cited by 2
Heiter, J., Kemp, M. W., Spiller, O. B., Singer, D., Newnham, J. P., Kallapur, S. G., Jobe, A. H., & Kramer, B. W. W. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1150208 · Cited by 2
Metadata
- Authors
- Jessen, K., & Mirsky, R.
- Affiliations
- University College London (GB)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1983-11-01
- Volume
- 3
- Issue
- 11
- Pages
- 2206-2218
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6564643
- OpenAlex
- W1495439714
- Cited by
- 246
- References
- 1
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 8 · 2023: 7 · 2022: 11 · 2021: 7 · 2020: 5 · 2019: 6 · 2018: 8 · 2017: 4 · 2016: 12 · 2015: 7 · 2014: 8 · 2013: 3 · 2012: 7
- FWCI
- 14.97
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Medical Research Council
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- enteric glial cells, enteric nervous system, glial fibrillary acidic protein, glutamine synthetase, vimentin, fibronectin, galactocerebroside, myenteric plexus, submucosal plexus, peripheral glia, glial cell culture
- MeSH terms
- Animals, Antigens, Surface, Astrocytes, Fibronectins, Fluorescent Antibody Technique, Galactosylceramides, Glial Fibrillary Acidic Protein, Glutamate-Ammonia Ligase, Histocytochemistry, Intermediate Filament Proteins, Intestine, Small, Neuroglia, Peripheral Nerves, Surface Properties, Vimentin, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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