4.5 Article

BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons

期刊

PHYSIOLOGICAL GENOMICS
卷 27, 期 3, 页码 391-397

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.00092.2006

关键词

choline acetyltransferase; bacterial artificial chromosome; acetylcholine

资金

  1. NHLBI NIH HHS [HL-45239, HL-76999] Funding Source: Medline
  2. NIDDK NIH HHS [DK-65992] Funding Source: Medline

向作者/读者索取更多资源

BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons. Physiol Genomics 27: 391-397, 2006. First published August 29, 2006; doi: 10.1152/physiolgenomics. 00092.2006. - The peripheral nervous system has complex and intricate ramifications throughout many target organ systems. To date this system has not been effectively labeled by genetic markers, due largely to inadequate transcriptional specification by minimum promoter constructs. Here we describe transgenic mice in which enhanced green fluorescent protein (eGFP) is expressed under the control of endogenous choline acetyl-transferase (ChAT) transcriptional regulatory elements, by knock-in of eGFP within a bacterial artificial chromosome (BAC) spanning the ChAT locus and expression of this construct as a transgene. eGFP is expressed in ChAT(BAC)-eGFP mice in central and peripheral cholinergic neurons, including cell bodies and processes of the somatic motor, somatic sensory, and parasympathetic nervous system in gastrointestinal, respiratory, urogenital, cardiovascular, and other peripheral organ systems. Individual epithelial cells and a subset of lymphocytes within the gastrointestinal and airway mucosa are also labeled, indicating genetic evidence of acetylcholine biosynthesis. Central and peripheral neurons were observed as early as 10.5 days postcoitus in the developing mouse embryo. ChAT(BAC)-eGFP mice allow excellent visualization of all cholinergic elements of the peripheral nervous system, including the submucosal enteric plexus, preganglionic autonomic nerves, and skeletal, cardiac, and smooth muscle neuromuscular junctions. These mice should be useful for in vivo studies of cholinergic neurotransmission and neuromuscular coupling. Moreover, this genetic strategy allows the selective expression and conditional inactivation of genes of interest in cholinergic nerves of the central nervous system and peripheral nervous system.

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