Glutaminolysis is Essential for Energy Production and Ion Transport in Human Corneal Endothelium

被引:53
作者
Zhang, Wenlin [1 ]
Li, Hongde [2 ]
Ogando, Diego G. [1 ]
Li, Shimin [1 ]
Feng, Matthew [3 ]
Price, Francis W., Jr. [3 ]
Tennessen, Jason M. [2 ]
Bonanno, Joseph A. [1 ]
机构
[1] Indiana Univ, Sch Optometry, Bloomington, IN 47405 USA
[2] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
[3] Price Vis Grp, Indianapolis, IN 46260 USA
关键词
Glutaminolysis; Energy metabolism; Corneal endothelium; SLC4A11 ammonia transporter; Congenital hereditary endothelial dystrophy (CHED); Fuchs' endothelial corneal dystrophy (FECD); PHOSPHATE-ACTIVATED GLUTAMINASE; GAMMA-GLUTAMYL-TRANSPEPTIDASE; PENETRATING KERATOPLASTY; SLC4A11; MUTATIONS; FLUID TRANSPORT; METABOLISM; GLUCOSE; EXTRACTION; EXPRESSION; PUMP;
D O I
10.1016/j.ebiom.2017.01.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Corneal endothelium (CE) is among the most metabolically active tissues in the body. This elevated metabolic rate helps the CE maintain corneal transparency by its ion and fluid transport properties, which when disrupted, leads to visual impairment. Here we demonstrate that glutamine catabolism(glutaminolysis) through TCA cycle generates a large fraction of the ATP needed to maintain CE function, and this glutaminolysis is severely disrupted in cells deficient in NH3:H+ cotransporter Solute Carrier Family 4 Member 11 (SLC4A11). Considering SLC4A11 mutations leads to corneal endothelial dystrophy and sensorineural deafness, our results indicate that SLC4A11-associated developmental and degenerative disorders result from altered glutamine catabolism. Overall, our results describe an important metabolic mechanism that provides CE cells with the energy required to maintain high level transport activity, reveal a direct link between glutamine metabolism and developmental and degenerative neuronal diseases, and suggest an approach for protecting the CE during ophthalmic surgeries. (C) 2017 The Authors. Published by Elsevier B.V.
引用
收藏
页码:292 / 301
页数:10
相关论文
共 52 条
[1]   Metabolic reprogramming during neuronal differentiation [J].
Agostini, M. ;
Romeo, F. ;
Inoue, S. ;
Niklison-Chirou, M. V. ;
Elia, A. J. ;
Dinsdale, D. ;
Morone, N. ;
Knight, R. A. ;
Mak, T. W. ;
Melino, G. .
CELL DEATH AND DIFFERENTIATION, 2016, 23 (09) :1502-1514
[2]  
Alleyne G A, 1982, Ciba Found Symp, V87, P101, DOI 10.1002/9780470720691.ch6
[3]   ELECTRICAL POTENTIAL AND FLUID TRANSPORT ACROSS CORNEAL ENDOTHELIUM [J].
BARFORT, P ;
MAURICE, D .
EXPERIMENTAL EYE RESEARCH, 1974, 19 (01) :11-19
[4]   Molecular mechanisms underlying the corneal endothelial pump [J].
Bonanno, Joseph A. .
EXPERIMENTAL EYE RESEARCH, 2012, 95 (01) :2-7
[5]  
Boonstra F, 2002, Ophthalmic Genet, V23, P247, DOI 10.1076/opge.23.4.247.13882
[6]   Biology of the corneal endothelium in health and disease [J].
Bourne, WM .
EYE, 2003, 17 (08) :912-918
[7]  
Bozkir G, 1997, ACTA MED OKAYAMA, V51, P9
[8]   CORNEAL DECOMPENSATION IN MITOCHONDRIAL OPHTHALMOPLEGIA PLUS (KEARNS-SAYRE) SYNDROME - A CLINICOPATHOLOGICAL CASE-REPORT [J].
CHANG, TS ;
JOHNS, DR ;
STARK, WJ ;
DRACHMAN, DB ;
GREEN, WR .
CORNEA, 1994, 13 (03) :269-273
[9]   High Throughput Gene Expression Analysis Identifies Reliable Expression Markers of Human Corneal Endothelial Cells [J].
Chng, Zhenzhi ;
Peh, Gary S. L. ;
Herath, Wishva B. ;
Cheng, Terence Y. D. ;
Ang, Heng-Pei ;
Toh, Kah-Peng ;
Robson, Paul ;
Mehta, Jodhbir S. ;
Colman, Alan .
PLOS ONE, 2013, 8 (07)
[10]   REGULATION OF GLUTAMINASE ACTIVITY AND GLUTAMINE-METABOLISM [J].
CURTHOYS, NP ;
WATFORD, M .
ANNUAL REVIEW OF NUTRITION, 1995, 15 :133-159