Acidic extracellular pH shifts colorectal cancer cell death from apoptosis to necrosis upon exposure to propionate and acetate, major end-products of the human probiotic propionibacteria

被引:109
作者
Lan, Annaig
Lagadic-Gossmann, Dominique
Lemaire, Christophe
Brenner, Catherine
Jan, Gwenael
机构
[1] UMR Sci & Technol Lait & Oeuf 1253, F-35042 Rennes, France
[2] Labs Standa, F-14050 Caen 4, France
[3] Univ Rennes 1, INSERM U620, Fac Pharm, F-35043 Rennes, France
[4] Univ Versailles, CNRS, UMR 8159, LGBC, F-78035 Versailles, France
关键词
cell death; colorectal cancer; short-chain fatty acids;
D O I
10.1007/s10495-006-0010-3
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
The human probiotic Propionibacterium freudenreichii kills colorectal adenocarcinoma cells through apoptosis in vitro via its metabolites, the short chain fatty acids (SCFA), acetate and propionate. However, the precise mechanisms, the kinetics of cellular events and the impact of environmental factors such as pH remained to be specified. For the first time, this study demonstrates a major impact of a shift in extracellular pH on the mode of propionibacterial SCFA-induced cell death of HT-29 cells, in the pH range 5.5 to 7.5 prevailing within the colon. Propionibacterial SCFA triggered apoptosis in the pH range 6.0 to 7.5, a lethal process lasting more than 96 h. Indeed at pH 7.5, SCFA induced cell cycle arrest in the G2/M phase, followed by a sequence of cellular events characteristic of apoptosis. By contrast, at pH 5.5, the same SCFA triggered a more rapid and drastic lethal process in less than 24 h. This was characterised by sudden mitochondrial depolarisation, inner membrane permeabilisation, drastic depletion in ATP levels and ROS accumulation, suggesting death by necrosis. Thus, in digestive cancer prophylaxis, the observed pH-mediated switch between apoptosis and necrosis has to be taken into account in strategies involving SCFA production by propionibacteria to kill colon cancer cells.
引用
收藏
页码:573 / 591
页数:19
相关论文
共 64 条
[1]   Necrotic volume increase and the early physiology of necrosis [J].
Barros, LF ;
Hermosilla, T ;
Castro, J .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR AND INTEGRATIVE PHYSIOLOGY, 2001, 130 (03) :401-409
[2]  
Belzacq AS, 2001, CANCER RES, V61, P1260
[3]   Apoptosis induced by the histone deacetylase inhibitor sodium butyrate in human leukemic lymphoblasts [J].
Bernhard, D ;
Ausserlechner, MJ ;
Tonko, M ;
Löffler, M ;
Hartmann, BL ;
Csordas, A ;
Kofler, R .
FASEB JOURNAL, 1999, 13 (14) :1991-2001
[4]   The fibre-folate debate in colo-rectal cancer [J].
Bingham, S .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2006, 65 (01) :19-23
[5]   Programmed cell death via mitochondria: Different modes of dying [J].
Bras, M ;
Queenan, B ;
Susin, SA .
BIOCHEMISTRY-MOSCOW, 2005, 70 (02) :231-+
[6]   Apoptosis - Mitochondria - the death signal integrators [J].
Brenner, C ;
Kroemer, G .
SCIENCE, 2000, 289 (5482) :1150-1151
[7]   Cell death independent of caspases:: A review [J].
Bröker, LE ;
Kruyt, FAE ;
Giaccone, G .
CLINICAL CANCER RESEARCH, 2005, 11 (09) :3155-3162
[8]   Acidic pH inhibits ATP depletion-induced tubular cell apoptosis by blocking caspase-9 activation in apoptosome [J].
Brooks, C ;
Ketsawatsomkron, P ;
Sui, Y ;
Wang, JZ ;
Wang, CY ;
Yu, FS ;
Dong, Z .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2005, 289 (02) :F410-F419
[9]   The role of disturbed pH dynamics and the Na+/H+ exchanger in metastasis [J].
Cardone, RA ;
Casavola, V ;
Reshkin, SJ .
NATURE REVIEWS CANCER, 2005, 5 (10) :786-795
[10]   A role for tumor necrosis factor receptor-2 and receptor-interacting protein in programmed necrosis and antiviral responses [J].
Chan, FKM ;
Shisler, J ;
Bixby, JG ;
Felices, M ;
Zheng, LX ;
Appel, M ;
Orenstein, J ;
Moss, B ;
Lenardo, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (51) :51613-51621