Natalie F. Barley
Imperial College London
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Featured researches published by Natalie F. Barley.
Journal of Bone and Mineral Research | 2006
Julian R. Walters; Sara Balesaria; Konstantia Maria Chavele; Vivienne Taylor; J.L. Berry; Umma Khair; Natalie F. Barley; David A. van Heel; Jennifer Field; Jamal O. Hayat; Abhik Bhattacharjee; Rosemary Jeffery; Richard Poulsom
Intestinal absorption of calcium affects bone mineralization and varies greatly. In human duodenum, expression of the calcium channel TRPV6 was directly related to blood 1,25‐dihydroxyvitamin D in men, but effects of age with lower median vitamin D receptor levels were more significant in women.
European Journal of Gastroenterology & Hepatology | 2008
Sara Balesaria; Robert J. Pell; Lucy J. Abbott; Ali M. Tasleem; Konstantia-Marie Chavele; Natalie F. Barley; Umma Khair; Alex Simon; Kieran J. Moriarty; W. Gordon Brydon; Julian R. Walters
Objectives Chronic diarrhoea resulting from primary idiopathic bile acid malabsorption (IBAM) is common, but its aetiology is largely unknown. We investigated possible mechanisms, first looking for common sequence variations in the cytoplasmic ileal bile acid-binding protein (IBABP, gene symbol FABP6), and secondly, determining the expression of ileal mucosal transcripts for the apical sodium-linked bile acid transporter (ASBT), IBABP, the putative basolateral transporters, OST&agr; and OST&bgr;, and regulatory factors. Methods Genomic DNA was prepared from two cohorts of patients and two control groups; the promoter and exonic regions of FABP6 were sequenced. In intestinal biopsies, transcript expression was measured by quantitative real time-PCR, using ileum from 17 patients and 21 controls. Results Sequence variations were identified in FABP6, but overall frequencies were similar in patients and controls. Transcripts of ASBT and IBABP, but not OST&agr; and OST&bgr;, were expressed at higher levels in ileum than duodenum. The transcription factors farnesoid-X-receptor (FXR) and liver-receptor-homologue (LRH-1) were also more abundant in ileum, as was fibroblast growth factor 19 (FGF19), unlike short heterodimer partner (SHP), c-Fos, or CDX2. No significant differences in mean or median values were found between the groups for any of these transcripts. However, findings on regression analysis suggested that these transporters differ in their regulation, particularly in the relationships of CDX2, LRH-1 and FXR with OST&agr;. Conclusion Most cases of IBAM are unlikely to be caused by genetic variation in FABP6 or by major differences in transporter transcript expression. Our evidence indicates that other factors, such as regulation of expression of the basolateral bile acid transporter, should be considered as possible causes.
The Journal of Steroid Biochemistry and Molecular Biology | 2004
Julian R. Walters; Natalie F. Barley; Mohammed Khanji; Orli Rhodes-Kendler
Intestinal absorption of dietary calcium is regulated by 1,25-dihydroxycholecalciferol (1,25(OH)(2)D(3)) in humans and in experimental animals but interspecies differences in responsiveness to 1,25(OH)(2)D(3) are found, possibly due to differences in the promoters of genes for intestinal calcium transport proteins or of the Vitamin D receptor (VDR). The epithelial calcium transporter, known as ECAC2 or CAT1, the product of the TRPV6 gene expressed in proximal intestinal enterocytes, is the first step in calcium absorption and studies in mice have shown that its expression is Vitamin D-dependent. In contrast in man, we showed that duodenal TRPV6 mRNA expression was independent of blood 1,25(OH)(2)D(3), although in Caco-2 cells, 1,25(OH)(2)D(3)-dependent changes have been demonstrated. We sought to explain these findings. A consensus Vitamin D response element in the mouse gene is absent in the human gene. We re-analysed our duodenal expression data according to a CDX2-site polymorphism in the VDR promoter. Mean TRPV6 expression was the same, but there was evidence of different responsiveness to 1,25(OH)(2)D(3). In the GG genotype group, but not the AG, duodenal TRPV6 expression increased with 1,25(OH)(2)D(3). We postulate that lower levels of expression of VDR in the GG group produce greater sensitivity to 1,25(OH)(2)D(3).
American Journal of Physiology-gastrointestinal and Liver Physiology | 2001
Natalie F. Barley; Alison Howard; David O'Callaghan; Stephen Legon; Julian R. Walters
Biochemical Journal | 1999
Natalie F. Barley; S. R. Prathalingam; P. Zhi; Stephen Legon; Alison Howard; Julian R. Walters
American Journal of Physiology-gastrointestinal and Liver Physiology | 2000
Paul Kitchen; Anthony J. FitzGerald; Robert A. Goodlad; Natalie F. Barley; M. A. Ghatei; Stephen Legon; S.R. Bloom; Ashley B. Price; Julian R. Walters; Alastair Forbes
Biochimica et Biophysica Acta | 2003
Natalie F. Barley; Vivienne Taylor; Charles J. Shaw-Smith; Probir Chakravarty; Alison Howard; Stephen Legon; Julian R. Walters
Analytical Biochemistry | 1998
S.Radhika Prathalingam; Alison Howard; Natalie F. Barley; Stephen Legon; Julian R. Walters
Gastroenterology | 2003
Julian R. Walters; Mohammed Khanji; Natalie F. Barley; Orli Rhodes-Kendler; Umma Khair
Gastroenterology | 2001
Natalie F. Barley; David O'Callaghan; Alison Howard; Stephen Legon; Julian R. Walters