Suggested functions for prolyl oligopeptidase:: A puzzling paradox

被引:75
作者
Brandt, Inger [1 ]
Scharpe, Simon [1 ]
Lambeir, Anne-Marie [1 ]
机构
[1] Univ Antwerp VIB, Dept Pharmaceut Sci, Med Biochem Lab, B-2610 Antwerp, Wilrijk, Belgium
关键词
prolyl oligopeptidase; serine protease; inositolphosphate; brain; neuropeptide;
D O I
10.1016/j.cca.2006.09.001
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Prolyl oligopeptidase (PO, E.C. 3.4.21.26) is a post-proline cleaving enzyme with endopeptidase activity towards peptides not longer than 30 amino acids. It has been purified and characterized from various mammalian and bacterial sources, but despite its thorough enzymological and structural characterization, the exact function of PO remains obscure. Many investigations have addressed the physiological role of this enzyme, mainly by the use of specific PO inhibitors, activity measurements in clinical samples and (neuro)peptide degradation studies. From the combined results emerges a puzzling paradox: how can an intracellular, cytoplasmatic oligopeptidase affect not only the amount of extracellular neuropeptides but also signal transduction and secretion? This report provides a review of the literature on the suggested functions for PO, highlighting possible pitfalls and contradictions. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:50 / 61
页数:12
相关论文
共 113 条
[101]   Pyroglutamyl peptidase I and prolyl endopeptidase in human semen:: increased activity in necrozoospermia [J].
Valdivia, A ;
Irazusta, J ;
Fernández, D ;
Múgica, J ;
Ochoa, C ;
Casis, L .
REGULATORY PEPTIDES, 2004, 122 (02) :79-84
[102]   Serum activity of prolyl endopeptidase, but not of dipeptidyl peptidase IV, is decreased by immunotherapy with IFN-α in high-risk melanoma patients [J].
Van Gool, AR ;
Van Ojik, HH ;
Kruit, WHJ ;
Mulder, PGH ;
Fekkes, D ;
Bannink, M ;
Scharpé, S ;
Stoter, G ;
Eggermont, AMM ;
Maes, M ;
Verkerk, R .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2004, 24 (07) :411-415
[103]   Evolutionary relationships of the prolyl oligopeptidase family enzymes [J].
Venäläinen, JI ;
Juvonen, RO ;
Männistö, PT .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2004, 271 (13) :2705-2715
[104]   PARTIAL-PURIFICATION AND CHARACTERIZATION OF POST-PROLINE CLEAVING ENZYME - ENZYMATIC INACTIVATION OF NEUROHYPOPHYSEAL HORMONES BY KIDNEY PREPARATIONS OF VARIOUS SPECIES [J].
WALTER, R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 422 (01) :138-158
[105]   EVIDENCE THAT PROLYL ENDOPEPTIDASE PARTICIPATES IN THE PROCESSING OF BRAIN ANGIOTENSIN [J].
WELCHES, WR ;
SANTOS, RAS ;
CHAPPELL, MC ;
BROSNIHAN, KB ;
GREENE, LJ ;
FERRARIO, CM .
JOURNAL OF HYPERTENSION, 1991, 9 (07) :631-638
[106]   Lithium therapy and signal transduction [J].
Williams, RSB ;
Harwood, AJ .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2000, 21 (02) :61-64
[107]   Pharmacogenetics in model systems: Defining a common mechanism of action for mood stabilisers [J].
Williams, RSB .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2005, 29 (06) :1029-1037
[108]   Loss of a prolyl oligopeptidase confers resistance to lithium by elevation of inositol (1,4,5) trisphosphate [J].
Williams, RSB ;
Eames, M ;
Ryves, WJ ;
Viggars, J ;
Harwood, AJ .
EMBO JOURNAL, 1999, 18 (10) :2734-2745
[109]   A common mechanism of action for three mood-stabilizing drugs [J].
Williams, RSB ;
Cheng, LL ;
Mudge, AW ;
Harwood, AJ .
NATURE, 2002, 417 (6886) :292-295
[110]   Early prepubertal ontogeny of pulsatile gonadotropin-releasing hormone (GnRH) secretion: I. Inhibitory autofeedback control through prolyl endopeptidase degradation of GnRH [J].
Yamanaka, C ;
Lebrethon, MC ;
Vandersmissen, E ;
Gerard, A ;
Purnelle, G ;
Lemaitre, M ;
Wilk, S ;
Bourguignon, JP .
ENDOCRINOLOGY, 1999, 140 (10) :4609-4615