The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Human CD4+CD25+ regulatory T cells selectively express tyrosine hydroxylase and contain endogenous catecholamines subserving an autocrine/paracrine inhibitory functional loop
Abstract
CD4+CD25+ regulatory T lymphocytes (Tregs) are specialized T cells playing a key role in the control of immune homeostasis. Here, we show that human Tregs constitutively express tyrosine hydroxylase (TH, EC 1.14.16.2), the rate-limiting enzyme in the synthesis of catecholamines, and contain substantial amounts of dopamine, norepinephrine, and epinephrine, which are released upon treatment with reserpine. Catecholamine release results in reduced production of interleukin-10 and transforming growth factor-β by Tregs, and in down-regulation of Treg-dependent inhibition of effector T-lymphocyte (Teff) proliferation, which occurs without affecting the production of tumor necrosis factor-α or interferon-γ. Tregs and Teffs express on the cell membrane both D1-like and D2-like dopaminergic receptors to a similar extent (12%-29% of the cells). Catecholamine-dependent down-regulation of Tregs is, however, selectively reversed by pharmacological blockade of dopaminergic D1-like receptors, which in Tregs only (and not in Teffs) are also expressed at the level of mRNA and are functionally coupled to intracellular production of cAMP. These findings indicate that in human Tregs endogenous catecholamines subserve an autocrine/paracrine loop involving dopaminergic pathways and resulting in down-regulation of Treg function.
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.
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
Regulatory T cells and tolerogenic dendritic cells: from basic biology to clinical applications
Rutella, S., & Lemoli, R. M. (2004) · Immunology Letters · doi:10.1016/j.imlet.2004.04.015 · Cited by 147
Research works printed but not linked: 62
- Sakaguchi S. Naturally arising CD4+ regulatory T cells for immunologic self-tolerance and negative control of the immune response. Annu Rev Immunol2004; 22:531–562.
- Thompson C and Powrie F. Regulatory T cells. Curr Op Pharmacol2004; 4:408–414. · DOI · Paper page
- Piccirillo CA and Thornton AM. Cornerstone of peripheral tolerance: naturally occurring CD4+CD25+ regulatory T cells. Trends Immunol2004; 25:374–380. · DOI · Paper page
- Walker LSK. CD4+ CD25+ Treg: divide and rule? Immunology2004; 111:129–137. · DOI
- Josefsson E, Bergquist J, Ekman R, Tarkowski A. Catecholamines are synthesized by mouse lymphocytes and regulate function of these cells by induction of apoptosis. Immunology1996; 88:140–146. · DOI · Paper page
- Spengler RN, Chensue SW, Giacherio DA, Blenk N, Kunkel SL. Endogenous norepinephrine regulates tumor necrosis factor-alpha production from macrophages in vitro. J Immunol1994; 152:3024–3031. · DOI · Paper page
- Freeman JG, Ryan JJ, Shelburne CP, et al. Catecholamines in murine bone marrow derived mast cells. J Neuroimmunol2001; 119:231–238. · DOI
- Musso NR, Brenci S, Setti M, Indiveri F, Lotti G. Catecholamine content and in vitro catecholamine synthesis in peripheral human lymphocytes. J Clin Endocrinol Metab1996; 81:3553–3557. · DOI
- Bergquist J and Silberring J. Identification of catecholamines in the immune system by electrospray ionization mass spectrometry. Rapid Commun Mass Spectrom1998; 12:683–688. · doi:10.1002/(sici)1097-0231(19980615)12:11<683::aid-rcm218>3.3.co;2-e
- Marino F, Cosentino M, Bombelli R, Ferrari M, Lecchini S, Frigo G. Endogenous catecholamine synthesis, metabolism storage, and uptake in human peripheral blood mononuclear cells. Exp Hematol1999; 27:489–495. · DOI
- Bergquist J, Tarkowski A, Ekman R, Ewing A. Discovery of endogenous catecholamines in lymphocytes and evidence for catecholamine regulation of lymphocyte function via an autocrine loop. Proc Natl Acad Sci U S A1994; 91:12912–12916. · DOI · Paper page
- Cosentino M, Marino F, Bombelli R, Ferrari M, Lecchini S, Frigo G. Endogenous catecholamine synthesis, metabolism, storage and uptake in human neutrophils. Life Sci1999; 64:975–981. · DOI
- Cosentino M, Bombelli R, Ferrari M, et al. HPLC-ED measurement of endogenous catecholamines in human immune cells and hematopoietic cell lines. Life Sci2000; 68:283–295. · DOI
- Tsao CW, Lin YS, Cheng JT. Inhibition of immune cell proliferation with haloperidol and relationship of tyrosine hydroxylase expression to immune cell growth. Life Sci1998; 62:335–344. · doi:10.1016/s0024-3205(98)00170-2
- Cosentino M, Marino F, Bombelli R, et al. Stimulation with phytohaemagglutinin induces the synthesis of catecholamines in human peripheral blood mononuclear cells: role of protein kinase C and contribution of intracellular calcium. J Neuroimmunol2002; 125:125–133. · DOI
- Ferrari M, Cosentino M, Marino F, et al. Dopaminergic D1-like receptor-dependent inhibition of tyrosine hydroxylase mRNA expression and catecholamine production in human lymphocytes. Biochem Pharmacol2004; 67:865–873. · DOI
- Cosentino M, Zaffaroni M, Marino F, et al. Catecholamine production and tyrosine hydroxylase expression in peripheral blood mononuclear cells from multiple sclerosis patients: effect of cell stimulation and possible relevance for activation-induced apoptosis. J Neuroimmunol2002; 133:233–240. · DOI
- Cosentino M, Marino F, Bombelli R, Ferrari M, Lecchini S, Frigo GM. Unravelling dopamine (and catecholamine) physiopharmacology in lymphocytes: open questions. Trends Immunol2003; 24:581–582. · DOI
- Kohm AP and Sanders VM. Norepinephrine and beta 2-adrenergic receptor stimulation regulate CD4+ T and B lymphocyte function in vitro and in vivo. Pharmacol Rev2001; 53:487–525. · DOI · Paper page
- Elenkov IJ, Wilder RL, Chrousos GP, Vizi ES. The sympathetic nerve: an integrative interface between two supersystems: the brain and the immune system. Pharmacol Rev2000; 52:595–638. · DOI · Paper page
- Levite M, Chowers Y, Ganor Y, Besser M, Hershkovits R, Cahalon L. Dopamine interacts directly with its D3 and D2 receptors on normal human T cells, and activates beta1 integrin function. Eur J Immunol2001; 31:3504–3512. · DOI
- McKenna F, McLaughlin PJ, Lewis BJ, et al. Dopamine receptor expression on human T- and B-lymphocytes, monocytes, neutrophils, eosinophils and NK cells: a flow cytometric study. J Neuroimmunol2002; 132:34–40. · DOI · Paper page
- Ilani T, Strous RD, Fuchs S. Dopaminergic regulation of immune cells via D3 dopamine receptor: a pathway mediated by activated T cells. FASEB J2004; 18:1600–1602. · DOI
- Besser MJ, Ganor Y, Levite M. Dopamine by itself activates either D2, D3 or D1/D5 dopaminergic receptors in normal human T-cells and triggers the selective secretion of either IL-10, TNFalpha or both. J Neuroimmunol2005; 169:161–171. · DOI · Paper page
- Watanabe Y, Nakayama T, Nagakubo D, et al. Dopamine selectively induces migration and homing of naive CD8+ T cells via dopamine receptor D3. J Immunol2006; 176:848–856. · DOI · Paper page
- Kin NW and Sanders VM. It takes nerve to tell T and B cells what to do. J Leukoc Biol2006; 79:1093–1104. · DOI · Paper page
- Basu S and Dasgupta PS. Dopamine, a neurotransmitter, influences the immune system. J Neuroimmunol2000; 102:113–124. · DOI · Paper page
- Saha B, Mondal AC, Majumder J, Basu S, Dasgupta PS. Physiological concentrations of dopamine inhibit the proliferation and cytotoxicity of human CD4+ and CD8+ T cells in vitro: a receptor-mediated mechanism. Neuroimmunomodulation2001; 9:23–33. · DOI
- Ghosh MC, Mondal AC, Basu S, et al. Dopamine inhibits cytokine release and expression of tyrosine kinases, Lck and Fyn in activated T cells. Int Immunopharmacol2003; 3:1019–1026. · DOI
- Kipnis J, Cardon M, Avidan H, et al. Dopamine, through the extracellular signal-regulated kinase pathway, downregulates CD4+CD25+ regulatory T-cell activity: implications for neurodegeneration. J Neurosci2004; 24:6133–6143. · DOI · Paper page
- Rouppe van der Voort C, Kavelaars A, van de Pol M, Heijnen C. Noradrenaline induces the phosphorylation of ERK-2 in human peripheral blood mononuclear cells after induction of α1-adrenergic receptors. J Neuroimmunol2000; 108:82–91. · DOI
- Zoukos Y, Kidd D, Woodroofe MN, Kendall BE, Thompson AJ, Cuzner ML. Increased expression of high affinity IL-2 receptors and β-adrenoceptors on peripheral blood mononuclear cells is associated with clinical and MRI activity in multiple sclerosis. Brain1994; 117:307–315. · DOI
- Hayashi M, Haga M, Yatsushiro S, Yamamoto A, Moriyama Y. Vesicular monoamine transporter 1 is responsible for storage of 5-hydroxytryptamine in rat pinealocytes. J Neurochem1999; 73:2538–2545. · DOI
- Vrana S, Kluttz B, Vrana K. Application of quantitative RT-PCR to the analysis of dopamine receptor mRNA levels in rat striatum. Mol Brain Res1995; 34:127–134. · DOI
- Segal D, Moraes C, Mash D. Up-regulation of D3 dopamine receptor mRNA in the nucleus accumbens of human cocaine fatalities. Mol Brain Res1997; 45:335–339. · DOI · Paper page
- Mulcrone J and Kerwin R. No difference in the expression of the D4 gene in post-mortem frontal cortex from controls and schizophrenics. Neurosci Lett1996; 219:163–166. · DOI
- Nagai Y, Ueno S, Saeki Y, Soga F, Hirano M, Yanagihara T. Decrease of the D3 dopamine receptor mRNA expression in lymphocytes from patients with Parkinson's disease. Neurology1996; 46:791–795. · DOI
- Ricci A, Bronzetti E, Conterno A, et al. alpha1-adrenergic receptor subtypes in human peripheral blood lymphocytes. Hypertension1999; 33:708–712. · DOI
- Viguerie N, Millet L, Avizou S, Vidal H, Larrouy D, Langin D. Regulation of human adipocyte gene expression by thyroid hormone. J Clin Endocrinol Metab2002; 87:630–634. · DOI
- Scriba D, Aprath-Husmann I, Blum WF, Hauner H. Catecholamines suppress leptin release from in vitro differentiated subcutaneous human adipocytes in primary culture via beta1- and beta2-adrenergic receptors. Eur J Endocrinol2000; 143:439–445. · DOI
- Garlet GP, Martins W Jr, Ferreira BR, Milanezi CM, Silva JS. Patterns of chemokines and chemokine receptors expression in different forms of human periodontal disease. J Periodontal Res2003; 38:210–217. · DOI · Paper page
- Saed GM, Collins KL, Diamond MP. Transforming growth factors beta1, beta2 and beta3 and their receptors are differentially expressed in human peritoneal fibroblasts in response to hypoxia. Am J Reprod Immunol2002; 48:387–393. · DOI
- Walker MR, Kasprowicz DJ, Gersuk VH, et al. Induction of FoxP3 and acquisition of T regulatory activity by stimulated human CD4+CD25- T cells. J Clin Invest2003; 112:1437–1443. · DOI · Paper page
- Seeman P. Brain dopamine receptors. Pharmacol Rev1980; 32:229–313.
- Seeman P and Van Tol HHM. Dopamine receptor pharmacology. Trends Pharmacol Sci1994; 15:264–270. · DOI · Paper page
- Torres KC, Antonelli LR, Souza AL, Teixeira MM, Dutra WO, Gollob KJ. Norepinephrine, dopamine and dexamethasone modulate discrete leukocyte subpopulations and cytokine profiles from human PBMC. J Neuroimmunol2005; 166:144–157. · DOI
- Ramer-Quinn DS, Baker RA, Sanders VM. Activated T helper 1 and T helper 2 cells differentially express the beta-2-adrenergic receptor: a mechanism for selective modulation of T helper 1 cell cytokine production. J Immunol1997; 159:4857–4867. · DOI · Paper page
- Andrade-Mena CE. Inhibition of gamma interferon synthesis by catecholamines. J Neuroimmunol1997; 76:10–14. · DOI
- Swanson MA, Lee WT, Sanders VM. IFN-γ production by Th1 cells generated from naive CD4+ T cells exposed to norepinephrine. J Immunol2001; 166:232–240. · DOI · Paper page
- Ramer-Quinn DS, Swanson MA, Lee WT, Sanders VM. Cytokine production by naive and primary effector CD4+ T cells exposed to norepinephrine. Brain Behav Immun2000; 14:239–255. · DOI
- Basu S and Dasgupta PS. Role of dopamine in malignant tumor growth. Endocrine2000; 12:237–241. · DOI
- Wick MM. Therapeutic effect of dopamine infusion on human malignant melanoma. Cancer Treat Rep1982; 66:1657–1659.
- FitzGerald GB and Wick MM. 3,4-Dihydroxybenzylamine: an improved dopamine analog cytotoxic for melanoma cells in part through oxidation products inhibitory to dna polymerase. J Invest Dermatol1983; 80:119–123. · DOI
- Lakshmi C, Deb C, Ray C, Ray MR. Reduction of hematotoxicity and augmentation of antitumor efficacy of cyclophosphamide by dopamine. Neoplasma2005; 52:68–73.
- Hiura T, Kagamu H, Miura S, et al. Both regulatory T cells and antitumor effector T cells are primed in the same draining lymph nodes during tumor progression. J Immunol2005; 175:5058–5066. · DOI
- Cosentino M, Zaffaroni M, Ferrari M, et al. Interferon-gamma and interferon-beta affect endogenous catecholamines in human peripheral blood mononuclear cells: implications for multiple sclerosis. J Neuroimmunol2005; 162:112–121. · DOI
- Wadler S. The role of interferons in the treatment of solid tumors. Cancer1992; 70:4 suppl, 949–958.
- Moschos S, Varanasi S, Kirkwood JM. Interferons in the treatment of solid tumors. Cancer Treat Res2005; 126:207–241. · DOI
- McMurray RW. Bromocriptine in rheumatic and autoimmune diseases. Semin Arthritis Rheum2001; 31:21–32. · DOI
- Sakic B, Lacosta S, Denburg JA, Szechtman H. Altered neurotransmission in brains of autoimmune mice: pharmacological and neurochemical evidence. J Neuroimmunol2002; 129:84–96. · DOI
- Giorelli M, Livrea P, Trojano M. Dopamine fails to regulate activation of peripheral blood lymphocytes from multiple sclerosis patients: effects of IFN-beta. J Interferon Cytokine Res2005; 25:395–406. · DOI
- Bergquist J, Josefsson E, Tarkowski A, Ekman R, Ewing A. Measurements of catecholamine-mediated apoptosis of immunocompetent cells by capillary electrophoresis. Electrophoresis1997; 18:1760–1766. · DOI
Cited by
Inflammation in Parkinson’s Disease: Mechanisms and Therapeutic Implications
Pajares, M., I. Rojo, A., Manda, G., Boscá, L., & Cuadrado, A. (2020) · Cells · doi:10.3390/cells9071687 · Cited by 779
The sympathetic nervous response in inflammation
Pongratz, G., & Straub, R. H. (2014) · Arthritis Research & Therapy · doi:10.1186/s13075-014-0504-2 · Cited by 427
ANISMAN, H., MERALI, Z., & HAYLEY, S. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.01.004 · Cited by 337
The immunoregulatory role of dopamine: An update
Sarkar, C., Basu, B., Chakroborty, D., Dasgupta, P. S., & Basu, S. (2010) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2009.10.015 · Cited by 323
Dopamine, Immunity, and Disease
Channer, B., Matt, S. M., Nickoloff-Bybel, E. A., Pappa, V., Agarwal, Y., Wickman, J., & Gaskill, P. J. (2023) · Pharmacological Reviews · doi:10.1124/pharmrev.122.000618 · Cited by 308
Metadata
- Authors
- Cosentino, M., Fietta, A. M., Ferrari, M., Rasini, E., Bombelli, R., Carcano, E., Saporiti, F., Meloni, F., Marino, F., & Lecchini, S.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2006-09-19
- Volume
- 109
- Issue
- 2
- Pages
- 632-642
- ISSN
- 0006-4971
- 1528-0020
- Cited by
- 278
- References
- 1
- Language
- en
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
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Human CD4+CD25+ regulatory T cells selectively express tyrosine hydroxylase and contain endogenous catecholamines subserving an autocrine/paracrine inhibitory functional loop. https://app.cochat.ai/papers/10.1182/blood-2006-01-028423
- The paper
- Cosentino, M., Fietta, A. M., Ferrari, M., Rasini, E., Bombelli, R., Carcano, E., Saporiti, F., Meloni, F., Marino, F., & Lecchini, S. (2007). Human CD4+CD25+ regulatory T cells selectively express tyrosine hydroxylase and contain endogenous catecholamines subserving an autocrine/paracrine inhibitory functional loop. Blood. https://doi.org/10.1182/blood-2006-01-028423
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.