Biology:Equilibrative nucleoside transporter family
Members of the Equilibrative Nucleoside Transporter (ENT) Family (TC# 2.A.57) are transport proteins that are specific to nucleosides and nucleobases, and are part of the major facilitator superfamily. They generally possess at least 6, typically 10, transmembrane segments (TMSs) and are 300-600 amino acyl residues in length.
Function
ENTs, including those in parasitic protozoa, function in nucleoside and nucleobase uptake for salvage pathways of nucleotide synthesis and, in humans, are also responsible for the cellular uptake of nucleoside analogues used in the treatment of cancers and viral diseases. By regulating the concentration of adenosine available to cell surface receptors, mammalian ENTs additionally influence physiological processes ranging from cardiovascular activity to neurotransmission.[1]
Human ENTs
In humans ENT are also known as SLC29, a group of plasmalemmal transport proteins which transport nucleoside substrates like adenosine into cells.[2] There are four known human ENTs, designated ENT1, ENT2, ENT3, and ENT4.[2][3] They are blocked by adenosine reuptake inhibitors like dipyridamole and dilazep, drugs used clinically for their vasodilatory properties.[3][4]
The best-characterized members of the human Ent family, hENT1 and hENT2, possess similar broad permeant selectivities for purine and pyrimidine nucleosides, but hENT2 also efficiently transports nucleobases.[5][6] hENT3 has a similar broad permeant selectivity for nucleosides and nucleobases and appears to function in intracellular membranes, including lysosomes. Gemcitabine, an anti-cancer drug, is transported by hENT1 and hENT3.[7] hENT4 is uniquely selective for adenosine, and also transports a variety of organic cations.
Transport reaction
The generalized transport reaction catalyzed by well characterized ENT family members is:
- Nucleoside (out) → Nucleoside (in)
See also
Further reading
- "Physiological and pharmacological roles of nucleoside transporter proteins". Nucleosides, Nucleotides & Nucleic Acids 27 (6): 769–78. Jun 2008. doi:10.1080/15257770802145819. PMID 18600539.
References
- ↑ Young, J. D.; Yao, S. Y. M.; Sun, L.; Cass, C. E.; Baldwin, S. A. (2008-07-01). "Human equilibrative nucleoside transporter (ENT) family of nucleoside and nucleobase transporter proteins". Xenobiotica 38 (7–8): 995–1021. doi:10.1080/00498250801927427. ISSN 1366-5928. PMID 18668437.
- ↑ 2.0 2.1 "The equilibrative nucleoside transporter family, SLC29". Pflügers Archiv 447 (5): 735–43. Feb 2004. doi:10.1007/s00424-003-1103-2. PMID 12838422.
- ↑ 3.0 3.1 "Nucleoside transporter proteins". Current Vascular Pharmacology 7 (4): 426–34. Oct 2009. doi:10.2174/157016109789043892. PMID 19485885. http://www.bentham-direct.org/pages/content.php?CVP/2009/00000007/00000004/002AD.SGM.
- ↑ "Adenosine uptake inhibitors". European Journal of Pharmacology 495 (1): 1–16. Jul 2004. doi:10.1016/j.ejphar.2004.05.003. PMID 15219815.
- ↑ Engel, Karen; Zhou, Mingyan; Wang, Joanne (2004-11-26). "Identification and characterization of a novel monoamine transporter in the human brain". The Journal of Biological Chemistry 279 (48): 50042–50049. doi:10.1074/jbc.M407913200. ISSN 0021-9258. PMID 15448143.
- ↑ Griffiths, Mark (15 Dec 1997). "Molecular cloning and characterization of a nitrobenzylthioinosine-insensitive (ei) equilibrative nucleoside transporter from human placenta.". Biochemical Journal 328 (3): 739–43. doi:10.1042/bj3280739. PMID 9396714.
- ↑ Orlandi, A.; Calegari, M. A.; Martini, M.; Cocomazzi, A.; Bagalà, C.; Indellicati, G.; Zurlo, V.; Basso, M. et al. (2016-10-01). "Gemcitabine versus FOLFIRINOX in patients with advanced pancreatic adenocarcinoma hENT1-positive: everything was not too bad back when everything seemed worse". Clinical & Translational Oncology 18 (10): 988–995. doi:10.1007/s12094-015-1471-z. ISSN 1699-3055. PMID 26742940.
As of this edit, this article uses content from [PASTE TCDB URL HERE "PASTE TCDB ARTICLE TITLE HERE"], which is licensed in a way that permits reuse under the Creative Commons Attribution-ShareAlike 3.0 Unported License, but not under the GFDL. All relevant terms must be followed.
 |  |
