Physiological roles for ecto-5′-nucleotidase (CD73)

被引:422
作者
Colgan S.P. [1 ]
Eltzschig H.K. [1 ,2 ]
Eckle T. [2 ]
Thompson L.F. [3 ]
机构
[1] Center for Experimental Therapeutics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, Thorn Building 704
[2] Department of Anesthesiology and Intensive Care Medicine, Tübingen University Hospital, Tübingen
[3] Immunobiology and Cancer Program, Oklahoma Medical Research Foundation, Oklahoma City
基金
美国国家卫生研究院;
关键词
Endothelia; Epithelia; Hypoxia; Inflammation; Nucleotidase; Nucleotide;
D O I
10.1007/s11302-005-5302-5
中图分类号
学科分类号
摘要
Nucleotides and nucleosides influence nearly every aspect of physiology and pathophysiology. Extracellular nucleotides are metabolized through regulated phosphohydrolysis by a series of ecto-nucleotidases. The formation of extracellular adenosine from adenosine 5′-monophosphate is accomplished primarily through ecto-5′-nucleotidase (CD73), a glycosyl phosphatidylinositol-linked membrane protein found on the surface of a variety of cell types. Recent in vivo studies implicating CD73 in a number of tissue protective mechanisms have provided new insight into its regulation and function and have generated considerable interest. Here, we review contributions of CD73 to cell and tissue stress responses, with a particular emphasis on physiologic responses to regulated CD73 expression and function, as well as new findings utilizing Cd73-deficient animals. © Springer 2006.
引用
收藏
页码:351 / 360
页数:9
相关论文
共 50 条
[41]   Hypoxia enhances Ecto-5′-Nucleotidase activity and cell surface expression in endothelial cells -: Role of membrane lipids [J].
Ledoux, S ;
Runembert, I ;
Koumanov, K ;
Michel, JB ;
Trugnan, G ;
Friedlander, G .
CIRCULATION RESEARCH, 2003, 92 (08) :848-855
[42]   Ectonucleoside triphosphate diphosphohydrolases and ecto-5′-nucleotidase in purinergic signaling: how the field developed and where we are now [J].
Zimmermann, Herbert .
PURINERGIC SIGNALLING, 2021, 17 (01) :117-125
[43]   Methotrexate and sulfasalazine promote adenosine release by a mechanism that requires ecto-5′-nucleotidase-mediated conversion of adenine nucleotides [J].
Morabito, L ;
Montesinos, MC ;
Schreibman, DM ;
Balter, L ;
Thompson, LF ;
Resta, R ;
Carlin, G ;
Huie, MA ;
Cronstein, BN .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (02) :295-300
[44]   Enzyme activity of circulating CD73 in human serum [J].
Morello, Silvana ;
Turiello, Roberta ;
Madonna, Gabriele ;
Pinto, Aldo ;
Ascierto, Paolo A. ;
Capone, Mariaelena .
TUMOR IMMUNOLOGY AND IMMUNOTHERAPY - MOLECULAR METHODS, 2019, 629 :257-267
[45]   Regulation of CD73 in the development of lower limb atherosclerosis [J].
Jalkanen, Juho ;
Hollmen, Maija ;
Jalkanen, Sirpa ;
Hakovirta, Harri .
PURINERGIC SIGNALLING, 2017, 13 (01) :127-134
[46]   Deletion of CD73 in mice leads to aortic valve dysfunction [J].
Zukowska, P. ;
Kutryb-Zajac, B. ;
Jasztal, A. ;
Toczek, M. ;
Zabielska, M. ;
Borkowski, T. ;
Khalpey, Z. ;
Smolenski, R. T. ;
Slominska, E. M. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2017, 1863 (06) :1464-1472
[47]   CD73: A Novel Target for Cancer Immunotherapy [J].
Zhang, Bin .
CANCER RESEARCH, 2010, 70 (16) :6407-6411
[48]   Ecto-5′-Nucleotidase, Adenosine and Transmembrane Adenylyl Cyclase Signalling Regulate Basal Carotid Body Chemoafferent Outflow and Establish the Sensitivity to Hypercapnia [J].
Holmes, Andrew P. ;
Nunes, Ana Rita ;
Cann, Martin J. ;
Kumar, Prem .
ARTERIAL CHEMORECEPTORS IN PHYSIOLOGY AND PATHOPHYSIOLOGY, 2015, 860 :279-289
[49]   Probiotic-Derived Ecto-5'-Nucleotidase Produces Anti-Inflammatory Adenosine Metabolites in Treg-Deficient Scurfy Mice [J].
Liu, Yuying ;
Armbrister, Shabba A. ;
Okeugo, Beanna ;
Mills, Tingting W. ;
Daniel, Rhea C. ;
Oh, Jee-Hwan ;
van Pijkeren, Jan-Peter ;
Park, Evelyn S. ;
Saleh, Zeina M. ;
Lahiri, Sharmistha ;
Roos, Stefan ;
Rhoads, JMarc .
PROBIOTICS AND ANTIMICROBIAL PROTEINS, 2023, 15 (04) :1001-1013
[50]   ALPHA(1)-ADRENOCEPTOR ACTIVATION INCREASES ECTO-5'-NUCLEOTIDASE ACTIVITY AND ADENOSINE RELEASE IN RAT CARDIOMYOCYTES BY ACTIVATING PROTEIN-KINASE-C [J].
KITAKAZE, M ;
HORI, M ;
MORIOKA, T ;
MINAMINO, T ;
TAKASHIMA, S ;
OKAZAKI, Y ;
NODE, K ;
KOMAMURA, K ;
IWAKURA, K ;
ITOH, T ;
INOUE, M ;
KAMADA, T .
CIRCULATION, 1995, 91 (08) :2226-2234