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Endocrine Abstracts (2004) 8 P38

SFE2004 Poster Presentations Diabetes, metabolism and cardiovascular (18 abstracts)

CHARACTERISATION OF ADRENOMEDULLIN RECEPTOR (CRLR/RAMP2) EXPRESSION IN HUMAN MICROVASCULAR ENDOTHELIAL CELLS

N Schwarz 1 , K Sidhu 2 , S Kapas 3 & JP Hinson 1


1Department of Endocrinology, Barts and the London, Queen Mary's School of Medicine and Dentistry, Suite 12, Dominion House, Bartholomew Close, London, EC1A 7BE, UK.; 2Department of Endocrinology, Barts and the London, Queen Mary's School of Medicine and Dentistry, Suite 14, Dominion House, Bartholomew Close, London, EC1A 7BE, UK.; 3Molecular Signalling Group, Clinical Sciences Research Center, Barts & the London, Queen Mary's School of Medicine & Dentistry, London, U.K.


Adrenomedullin (ADM) is a multifunctional peptide which plays a significant role in vasodilation, angiogenisis and septic shock. It exerts its effects via the calcitonin receptor-like receptor (CRLR) in combination with either receptor associated protein (RAMP) 2 or 3. However the regulation of the ADM receptors is still widely unknown (1). In the present study the effects of adrenomedullin on immortalized Human Microvascular Endothelial Cells (HMECs) was investigated. Endothelial cells are well established as a model for the study of ADM actions. We found for the first time in this cell line the expression of ADM receptor message and protein using PCR and western blotting respectively. Treatment of the cells with ADM elevated intracellular cAMP levels in a dose (10(super)-6(/super)-10(super)-9(/super)M) and time (5-45min) dependent manner. However in this study, this did not result in increased cell proliferation. The consequences of the raised cAMP levels are yet to be established. We further investigated the possible transcriptional activation of the RAMPs and CRLR in response to ADM stimulation, using semi-quantitative PCR. The results suggest that after 24 hours treatment with ADM (10(super)-7(/super)M) the transcription of CRLR is increased. Taken together with the already published characterisation of the CRLR promoter (2) these findings provide an explanation for the regulation of the adrenomedullin receptors.

References:

1.Hinson JP, Kapas S, Smith DM 2000 Adrenomedullin, a Multifunctional Regulatory Peptide. Endocrine Reviews 21(2): 138-1672.

2. Nikitenko LL, Smith DM, Bicknell R, Rees MC 2003 Transcriptional Regulation of the CRLR gene in human microvascular endothelial cells by hypoxia. FASEB J. Aug 17(11):1499-501

Volume 8

195th Meeting of the Society for Endocrinology joint with Diabetes UK and the Growth Factor Group

Society for Endocrinology 

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