The DOI matches its Crossref record; 116 of the 116 references it cites were found in a registry or an index.
Neuropod Cells: The Emerging Biology of Gut-Brain Sensory Transduction
Open accessAbstract
Guided by sight, scent, texture, and taste, animals ingest food. Once ingested, it is up to the gut to make sense of the food's nutritional value. Classic sensory systems rely on neuroepithelial circuits to convert stimuli into signals that guide behavior. However, sensation of the gut milieu was thought to be mediated only by the passive release of hormones until the discovery of synapses in enteroendocrine cells. These are gut sensory epithelial cells, and those that form synapses are referred to as neuropod cells. Neuropod cells provide the foundation for the gut to transduce sensory signals from the intestinal milieu to the brain through fast neurotransmission onto neurons, including those of the vagus nerve. These findings have sparked a new field of exploration in sensory neurobiology—that of gut-brain sensory transduction.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Enteroendocrine and enterochromaffin cells (ECCs) form close synaptic connections with certain vagal afferent fibers through cell extensions called neuropods [25, 26].”
From Role of diet and its effects on the gut microbiome in the pathophysiology of mental disorders (2022) · cites this paper as [25]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Bravo, J. A., Forsythe, P., Chew, M. V., Escaravage, E., Savignac, H. M., Dinan, T. G., Bienenstock, J., & Cryan, J. F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102999108 · Cited by 3,888 · cited 1×
“Moreover, other noninvasive gut microbes affect the central nervous system when delivered intraluminally, and their effects depend on an intact vagus nerve (Bravo et al. 2011, Sgritta et al. 2019).”
BackgroundHenry, M. A. (1995) · The Journal of the American Dental Association · doi:10.14219/jada.archive.1995.0108 · Cited by 3,454
Normal gut microbiota modulates brain development and behavior
Heijtz, R. D., Wang, S., Anuar, F., Qian, Y., Björkholm, B., Samuelsson, A., Hibberd, M. L., Forssberg, H., & Pettersson, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010529108 · Cited by 3,228 · cited 1×
“Germ-free mice, devoid of gut microbiota, have a host of neurological deficits (Diaz Heijtz et al. 2011).”
BackgroundTGR5-Mediated Bile Acid Sensing Controls Glucose Homeostasis
Thomas, C., Gioiello, A., Noriega, L., Strehle, A., Oury, J., Rizzo, G., Macchiarulo, A., Yamamoto, H., Mataki, C., Pruzanski, M., et al. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.08.001 · Cited by 1,885 · cited 1×
“Other classes of enteroendocrine cells that coexpress glucagon-like peptide 1 and peptide YY have been shown to be activated by indole (Chimerel et al. 2014) and bile acids (Thomas et al. 2009) and to co-release glucagon-like peptide 1 and ATP (Lu et al. 2019).”
BackgroundA single-cell survey of the small intestinal epithelium
Haber, A. L., Biton, M., Rogel, N., Herbst, R. H., Shekhar, K., Smillie, C., Burgin, G., Delorey, T. M., Howitt, M. R., Katz, Y., et al. (2017) · Nature · doi:10.1038/nature24489 · Cited by 1,750
Nelson, G., Chandrashekar, J. V., Hoon, M. A., Feng, L., Zhao, G., Ryba, N. J. P., & Zuker, C. S. (2002) · Nature · doi:10.1038/nature726 · Cited by 1,523 · cited 1×
“T1R1/T1R3 has also been shown to recognize other individual amino acids, suggesting that it could serve as a more generalized amino acid sensor (Daly et al. 2013, Nelson et al. 2002).”
BackgroundFunctional and chemical anatomy of the afferent vagal system
Berthoud, H.-R., & Neuhuber, W. L. (2000) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00215-0 · Cited by 1,280 · cited 1×
“The left and right vagi are composed of efferent and afferent rootlets, which exit the cranium via the jugular foramen, between the temporal and occipital bones (Berthoud & Neuhuber 2000).”
BackgroundThe mechanism of pancreatic secretion
Bayliss, W. M., & Starling, E. H. (1902) · The Journal of Physiology · doi:10.1113/jphysiol.1902.sp000920 · Cited by 1,274 · cited 2×
“[The concept of epithelial cell–specific postingestive sensing came about in the early twentieth century when Bayliss & Starling (1902) identified that a gut hormone, secretin, could be secreted following the presentation of luminal acid.]”
BackgroundGut-expressed gustducin and taste receptors regulate secretion of glucagon-like peptide-1.
Jang, H.-J., Kokrashvili, Z., Theodorakis, M. J., Carlson, O. D., Kim, B.-J., Zhou, J., Kim, H. H., Xu, X., Chan, S. L., Juhaszova, M., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706890104 · Cited by 995 · cited 1×
“Enteroendocrine cells are known to express taste receptors, particularly sweet taste receptors T1R2 andT1R3 ( Jang et al. 2007, Reimann et al. 2008).”
BackgroundA gut-brain neural circuit for nutrient sensory transduction
Kaelberer, M. M., Buchanan, K. L., Klein, M. E., Barth, B. B., Montoya, M. M., Shen, X., & Bohórquez, D. V. (2018) · Science · doi:10.1126/science.aat5236 · Cited by 932 · cited 6×
“More recently, it was discovered that enteroendocrine cells synapse with neurons largely originated from both the spinal cord dorsal root ganglia and the vagal nodose ganglia (Kaelberer et al. 2018).”
BackgroundInfluentialSelf-citation
Research works printed but not linked: 9
- Davison JS, 1988, Am. J. Physiol., 255, G55
- Lange CG, 1922, A Series of Reprints and Translations, Vol. 1: The Emotions
- Monnikes H, 1997, Am. J. Physiol., 273, R2059
- Pavlov IP., 1910, The Work of the Digestive Glands
- Phifer CB, 1998, Am. J. Physiol., 274, R1725
- Phillips RJ, 1998, Am. J. Physiol., 274, R1626
- Schwartz GJ, 1991, Am. J. Physiol., 261, R1141, 10.1152/ajpcell.1991.261.5.C793 · DOI
- Sidhu M, 1995, Am. J. Physiol., 269, G346
- Walls EK, 1995, Am. J. Physiol., 269, R1410
Cited by
Sorted by citations
Items 201–236 of 236
An “electric” microbial cue to control food intake behavior
Li, H., & Mucida, D. (2025) · Cell Metabolism · doi:10.1016/j.cmet.2025.09.007
Robust dual dynamics of ictogenesis in temporal lobe seizures in vivoPreprint
Mashiel, A., Achvat, S., & Schiller, Y. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.02.686119
Human Microbiome and Neurodevelopmental Disorders
Soni, J., Singh, M., Sharma, A., & Sen, A. (2025) · Springer eBooks · doi:10.1007/978-3-031-40858-8_588-1
NeuRoDev resolves lifelong temporal and cellular variation in human cortical gene expression
Zonca, A., Bot, E., & Dávila-Velderrain, J. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117374
Human Microbiome and Neurodevelopmental Disorders
Soni, J., Singh, M., Sharma, A., & Sen, A. (2025) · Springer eBooks · doi:10.1007/978-3-031-40858-8_588-2 · Cited by 1
Iida, N., Yoshida, Y., Iwasa, K., Kenta, A., Fujii, Y., Calabrese, V., Ohmoto, M., Abe, K., & Osakabe, N. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.6127970
Transcriptomic integration nominates FOXN2 as a candidate schizophrenia risk gene
Yu, L., Chen, J., Du, S., Long, Q., Guo, Z., Liu, Y. K., Qin, F., Wang, M., Luo, R., Zhang, Y., et al. (2026) · Behavioural Brain Research · doi:10.1016/j.bbr.2026.116068
Heng, Y., & Qiuming, Y. (2026) · Nutrition Clinique et Métabolisme · doi:10.1016/j.nupar.2026.103032
Lei, Y. J., Chen, C., Zhan, X., Xie, M., Wang, Y., Li, H., Zhang, J., & Liu, P. (2026) · Nature Communications · doi:10.1038/s41467-026-69924-w
“5 | Intestine-released ILPs regulate SRI-36 expression via the IIS pathway inADF. a – d Diacetyl-evokedGCaMP6responsesinADFneuronsofwormswiththe indicated genotypes and conditions.”
InfluentialPolyphenols and Sensory Nutrition
Osakabe, N. (2026) · Nippon Eiyo Shokuryo Gakkaishi · doi:10.4327/jsnfs.79.5
Gut-brain axis in metabolic control
Singh, S. P., Ghosh, S., Singh, D. K. K., & Sinha, J. K. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-32848-0.00024-8
Shen, Q., Lv, A., Li, Y., Liu, P., Yang, J., Wang, S., & Guo, H. (2026) · Neurogastroenterology & Motility · doi:10.1111/nmo.70289 · Cited by 1
“These cells form direct synaptic connections with vagal sensory terminals via specialized basolateral structures known as neuropods, establishing a gut–brain communication pathway that operates independently of classical neuronal circuits [112, 113].”
Gabriel-Segard, T. (2023) · theses.fr (ABES) · doi:10.70675/2f469c9fz7a22z4f47z9e37zcf0e1f890660
Yi, S., Qiwang, H. E., Yanan, L. I., & Bijiang, W. A. N. (2026) · Journal of Zhejiang University (Medical Sciences) · doi:10.3724/zdxbyxb-2025-0569
Intrinsic Primary Afferent Neurons of the Gastrointestinal Tract: Polyfunctional and Polymodal
Маслюков, П. М., Порсева, В. В., Будник, А. Ф., & Сальников, Е. В. (2026) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093026020134
Brain-Gut Interactions: Sensory Nutrition and Polyphenols
Osakabe, N., & Fujii, Y. (2026) · Springer eBooks · doi:10.1007/978-981-95-7068-3_54
Nowacka, A., Śniegocki, M., & Ziółkowska, E. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27115109
“The GUCY2C paradigm therefore extends neuropod-cell biology from nutrient sensing to direct regulation of visceral nociception [10,30,40,70,72,78,80].”
ZHANG, J.-J., Meng-Ya, F. A. N., & Shi-Feng, W. A. N. G. (2026) · Shengming kexue · doi:10.3724/cbls.2026089
Enteric neural-tumor interactions in gastrointestinal malignancies and therapeutic implications
Wang, S.-R., Cao, T.-L., Xia, Z.-A., & Jiang, H. (2026) · World Journal of Clinical Oncology · doi:10.5306/wjco.120495
Delgado‐Ocaña, S., Herrera, G., Guzman, D. D., Self, D. W., & Cuesta, S. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2693397
“83,84 In line with this idea, mice supplemented with exogenous glycine, while showing elevated amino acid levels in stool, displayed glycine levels in the NAc similar to those of untreated E. coli HS-colonized animals.”
Intestinal epithelial cells: Gatekeepers of the gut–brain axis, microbiome, and beyond
Wu, W.-L. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-40306-4.00018-1
Myc sustains sex-biased organ zonation in the Drosophila intestine
Amourda, C., Blackie, L., Gaspar, P., Martín-Coll, L., Prasad, A. R., House, A. H., Holopainen, M., Ruhanen, H., Lamichane, N., Hadjieconomou, D., et al. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.06.003
Yoshida, Y., Iida, N., Iwasa, K., Saito, A., Aso, K., Fujii, Y., Modafferi, S., Calabrese, V., Ohmoto, M., Abe, K., et al. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1863138
“Recent findings have further refined this model, revealing that a subset of EECs, termed “neuropod cells,” establish direct synaptic connections with nerves in the mucosa of the small intestine and colon (13).”
Breevoort, A., Ivanov, D., Horan-Portelance, L., Nana, A. L., Vatsavayai, S. C., Tudoras, À., Wallace, J. L., Ding, J. W., Pereira, F. L., Fernhoff, K., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.13.738307
Mental health and gut-brain crosstalk: implications for depression and Alzheimer's disease
Skourti, K., Katsaitis, F., Pavlidi, P., Anesti, M., Balla, J., Emvalomatis, A., Kokras, N., Dalla, C., & Sotiropoulos, I. (2026) · Neuroscience Applied · doi:10.1016/j.nsa.2026.107023
“This gut-to-brain sensory transmission is facilitated by specialized enteroendocrine cells (known as ‘neuropods ’ ) (Boh ´ orquez et al., 2015), which form synapses with vagal neurons, allowing fast and direct signaling from the gut to the brain (Kaelberer et al., 2020).”
Beyond flavor perception: The role of the taste receptor family in immunity
Ye, N., Wang, B., Cheng, Z., & Cheng, A. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.117184
EASI-PASS: An accessible pipeline for linking functional imaging and mRNA profilingPreprint
Alvarado, J. S., Massengill, C. I., Stern, J., Amsalem, O., Ventura, B. F., Jang, A., Cook, S., Veliche, A., Sunkavalli, P. S., Patel, D., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.21.746328
Microbiome and Diseases: Gut–Brain Axis and Neurological Disorders
de Castilhos, J., & Stein‐Thoeringer, C. K. (2026) · Springer eBooks · doi:10.1007/978-3-032-26410-7_18
The last‐step integrator thesis: Heterarchical control of the mammalian gastrointestinal tract
Bechtel, W., & Bich, L. (2026) · The Journal of Physiology · doi:10.1113/jp291403
“…inputs arise from some of the local control mechanisms we discussed above (in the case of neuroendocrine cells, they originate from extensions that have been designated neuropods; see Kaelberer et al., 2020), and the efferent outputs project back to them or directly to the production mechanisms.”
How the Sleeve Gastrectomy Works: Metabolically
Kachmar, M., Schauer, P. R., Aminian, A., & Albaugh, V. L. (2025) · Springer eBooks · doi:10.1007/978-3-031-77690-8_6-1
Lehner, T., Sandoval, D. A., & McCullough, R. L. (2026) · Alcohol · doi:10.1016/j.alcohol.2026.107460
Stepensky, D. (2026) · Pharmaceutics · doi:10.3390/pharmaceutics18101276
“Specialized enteroendocrine cells, termed neuropods, establish direct synaptic contact with vagal affer-ents, using glutamate and serotonin to relay microbial signals from the gut lumen to the brainstem (Level 3/4) [37,45].”
Luo, J., Li, X., Liu, B., Yu, Y., Shen, X., Liu, H., Hu, S., Luo, Q., Liang, X., Xiong, Y., et al. (2026) · Nutrients · doi:10.3390/nu18203371
“Luminal nutrients stimulate enteroendocrine cells to release cholecystokinin, glucagon-like peptide-1, and 5-HT, which activate vagal afferents to regulate appetite, energy balance, and fatigue perception [76,77].”
Self-citationFrom gut microbiome to aging brain: Butyrate as a neurogeroscience effector
Mitrea, L., Calinoiu, L.-F., Martau, G.-A., Teleky, B.-E., Cocean, A.-M., Odocheanu, R., Stefanescu, B.-E., & Vodnar, D.-C. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.107037
Diet and the microbiome–gut–brain axis: implications for clinical neuropsychology
Frame, L. A. (2026) · Archives of Clinical Neuropsychology · doi:10.1093/arclin/acag083
Jacquier‐Sarlin, M. R., Seignobos, M., Rauzier, L., Schaack, B., Laurin, D., & Buisson, A. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1963040
Metadata
- Authors
- Kaelberer, M. M., Rupprecht, L. E., Liu, W. W., Weng, P., & Bohórquez, D. V.
- Affiliations
- Duke University (US)
- Corresponding author
- Bohórquez, Diego V.
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 2020-07-08
- Volume
- 43
- Issue
- 1
- Pages
- 337-353
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- PMC
- PMC7573801
- OpenAlex
- W3007159566
- Cited by
- 236
- References
- 115
- Citations by year
- 2026: 44 · 2025: 58 · 2024: 43 · 2023: 36 · 2022: 26 · 2021: 22 · 2020: 7
- FWCI
- 3.99
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Duke-NUS Medical School
- National Institutes of Health (5r21at010818-02)
- National Institute of Mental Health (DP2MH122402)
- National Institute of General Medical Sciences (T32GM007171)
- National Center for Complementary and Integrative Health (R21-AT010818)
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Health Sciences › Nursing › Nutrition and Dietetics › Biochemical Analysis and Sensing Techniques
- Keywords
- enteroendocrine cells, synapses, neurotransmission, vagus nerve, intestinal hormones
- MeSH terms
- Animals, Brain, Humans, Neurons, Synapses, Vagus Nerve, Signal Transduction, Enteroendocrine Cells
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 ›
Are you an author, or do you see a problem with this page? Request a review