Prolylcarboxypeptidase: A cardioprotective enzyme

被引:46
作者
Mallela, J. [1 ]
Yang, J. [1 ]
Shariat-Madar, Z. [1 ]
机构
[1] Univ Mississippi, Sch Pharm, Dept Pharmacol, University, MS 38677 USA
关键词
ANGIOTENSINASE-C; GENE; RESPONSES;
D O I
10.1016/j.biocel.2008.02.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prolycarboxypeptidase (PRCP) is involved in regulating the blood flow through active tissues in order to preserve the internal environment. The expression of PRCP in tissues is determined by a number of pharmacological stimuli such as glucocorticoids and a combination of dexamethasone plus the mu-opioid receptor agonise [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate. PRCP is all enzyme which is associated with preeclampsia, rheumatoid arthritis, and tonsillitis. The interplay between inward cellular signalling required for induced and basal transcription, and PRCP expression have not been mechanistically characterized. Molecules modulated by PROP include angiotensin II (Ang II), angiotensin III (Ang III), alpha-MSH, and prekallikrein (PK), demonstrating its cardiovascular protective role. In addition to regulating vascular tone, PROP may modulate proliferation, cell migration, and angiogenesis through regulating angiotensin molecules - and bradykinin - induced endothelium activation. The anti-hypertensive and proinflammatory properties of PRCP implicate that this enzyme may well be all accessible target for anti-inflammatory therapy. Published by Elsevier Ltd.
引用
收藏
页码:477 / 481
页数:5
相关论文
共 20 条
[1]   Atrial fibrillation associated with hypokalemia due to primary hyperaldosteronism (Conn's syndrome) [J].
Aloul, Basel Al. ;
Li, Jian-Ming ;
Benditt, David ;
Tholakanahalli, Venkatakrishna .
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 2006, 29 (11) :1303-1305
[2]  
Catania Anna, 2003, Pediatr Endocrinol Rev, V1, P101
[3]   NEUROPHYSIOLOGICAL RESPONSES TO ANGIOTENSIN-(1-7) [J].
FELIX, D ;
KHOSLA, MC ;
BARNES, KL ;
IMBODEN, H ;
MONTANI, B ;
FERRARIO, CM .
HYPERTENSION, 1991, 17 (06) :1111-1114
[4]   Systemic effects of angiotensin III in conscious dogs during acute double blockade of the renin-angiotensin-aldosterone-system [J].
Gammelgaard, I. ;
Wamberg, S. ;
Bie, P. .
ACTA PHYSIOLOGICA, 2006, 188 (02) :129-138
[5]  
HOOLEY E, 2007, J THROMB HAEMOST
[6]   Protection from angiotensin II-induced cardiac hypertrophy and fibrosis by systemic lentiviral delivery of ACE2 in rats [J].
Huentelman, MJ ;
Grobe, JL ;
Vazquez, J ;
Stewart, JM ;
Mecca, AP ;
Katovich, MJ ;
Ferrario, CM ;
Raizada, MK .
EXPERIMENTAL PHYSIOLOGY, 2005, 90 (05) :783-790
[7]   PLASMA MEMBRANE-BOUND AND LYSOSOMAL PEPTIDASES IN HUMAN ALVEOLAR MACROPHAGES [J].
JACKMAN, HL ;
TAN, FL ;
SCHRAUFNAGEL, D ;
DRAGOVIC, T ;
DEZSO, B ;
BECKER, RP ;
ERDOS, EG .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 13 (02) :196-204
[8]   PROLYLCARBOXYPEPTIDASE (ANGIOTENSINASE-C) IN HUMAN-LUNG AND CULTURED-CELLS [J].
KUMAMOTO, K ;
STEWART, TA ;
JOHNSON, AR ;
ERDOS, EG .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 67 (01) :210-215
[9]  
ODYA CE, 1978, J BIOL CHEM, V253, P5927
[10]   Differential gene expression profile of human tonsil high endothelial cells: implications for lymphocyte trafficking [J].
Palmeri, D ;
Zuo, FR ;
Rosen, SD ;
Hemmerich, S .
JOURNAL OF LEUKOCYTE BIOLOGY, 2004, 75 (05) :910-927