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HPMR

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Solute Carrier Family 18, Member 3 OKDB#: 1115
 Symbols: SLC18A3 Species: human
 Synonyms: VESICULAR ACETYLCHOLINE TRANSPORTER, VACHT|  Locus: 10q11.2 in Homo sapiens
HPMR


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General Comment The vesicular acetylcholine transporter (VAChT) has been identified and characterized based on the acquisition of high affinity vesamicol binding and proton-dependent, vesamicol-sensitive acetylcholine accumulation by a fibroblast cell line transfected with a clone from a rat pheochromocytoma cDNA library encoding this protein Erickson JD et al 1994 . The distribution of VAChT mRNA coincides with that reported for choline acetyltransferase (ChAT), the enzyme required for acetylcholine biosynthesis, in the peripheral and central cholinergic nervous systems.

General function Receptor, Channel/transport protein
Comment
Cellular localization Plasma membrane
Comment
Ovarian function Follicle development, Antral follicle growth
Comment
Expression regulated by
Comment
Ovarian localization Granulosa, Luteal cells
Comment Fritz S, et al reported the evidence for expression of choline-acetyltransferase and vesicular acetylcholine transporter in human granulosa-luteal cells. The authors demonstrated the ability of muscarinic agonists to stimulate the proliferation of human GC within 24 h. In vivo, ACh, the natural ligand of these receptors is thought to be contained in cholinergic nerve fibers innervating the ovary. Surprisingly, the prerequisite for the synthesis of ACh, the enzyme choline-acetyltransferase (ChAT), is also expressed by human GC, as shown by Western blotting and immunocytochemistry. In addition, these cells express another marker for ACh synthesis, namely the gene for the vesicular acetylcholine transporter, as evidenced by RT-PCR cloning, Western blotting, and immunocytochemistry. The data identify the M1 receptor in human GC and point to a novel, trophic role of the neurotransmitter ACh. Furthermore, the presence of the prerequisites of ACh synthesis in human GC indicate that an autocrine/paracrine regulatory loop also exists in the in vivo counterparts of these cells in the ovary, i.e. in the cells of the preovulatory follicle and/or of the young corpus luteum.
Follicle stages Antral, Preovulatory
Comment
Phenotypes
Mutations 0 mutations
Genomic Region show genomic region
Phenotypes and GWAS show phenotypes and GWAS
Links
OMIM (Online Mendelian Inheritance in Man: an excellent source of general gene description and genetic information.)
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created: March 2, 2001, 3:43 p.m. by: hsueh   email:
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last update: Aug. 14, 2001, 9:19 a.m. by: hsueh    email:



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