IQUIFIB   02644
INSTITUTO DE QUIMICA Y FISICOQUIMICA BIOLOGICAS "PROF. ALEJANDRO C. PALADINI"
Unidad Ejecutora - UE
artículos
Título:
Beneficial activity of Enteroccocus faecaeis CECT7121 in the anti-limphoma protective response
Autor/es:
M.S. CASTRO; M.A. MOLINA; P. DI SCIULLO; M.B. AZPIROZ; F. LEOCATA NIETO; N.B. STERIN-SPEZIALE; C. MONGINI; M.A. MANGHI
Revista:
JOURNAL OF APPLIED MICROBIOLOGY
Editorial:
WILEY-BLACKWELL PUBLISHING, INC
Referencias:
Año: 2010 vol. 5072 p. 1234 - 1243
ISSN:
1364-5072
Resumen:
Abstract
Aims: To study the anti-tumour effects of Enterococcus faecalis CECT7121 on
LBC cells, an aggressive murine T-cell lymphoma that kills the host in 18 days
when is intraperitoneally (i.p.) administrated.To study the anti-tumour effects of Enterococcus faecalis CECT7121 on
LBC cells, an aggressive murine T-cell lymphoma that kills the host in 18 days
when is intraperitoneally (i.p.) administrated.
Methods and Results: In vitro studies have shown that LBC cell proliferation
was inhibited by Ent. faecalis CECT7121 stimulus in a dose-dependent manner,
inducing apoptosis. The production of ceramide was involved in the latter
effect. To undertake in vivo studies, syngeneic BALB ⁄ c mice pre-treated i.p.
with Ent. faecalis CECT7121 (2Æ5 · 108 CFU) were challenged i.p. with LBC
cells (1Æ0 · 106 cells) the day after. On day 30 post-inoculation of LBC cells,
70% of Ent. faecalis CECT7121 pre-treated mice survived, whereas no survivals
were recorded in the control group. A group of surviving mice was re-challenged
with LBC cells, and 89% of them survived. Upon stimulation with irradiated
LBC cells, spleen cell proliferation, high IFNc, IL-12 and IL-10 levels
were observed in surviving animals.In vitro studies have shown that LBC cell proliferation
was inhibited by Ent. faecalis CECT7121 stimulus in a dose-dependent manner,
inducing apoptosis. The production of ceramide was involved in the latter
effect. To undertake in vivo studies, syngeneic BALB ⁄ c mice pre-treated i.p.
with Ent. faecalis CECT7121 (2Æ5 · 108 CFU) were challenged i.p. with LBC
cells (1Æ0 · 106 cells) the day after. On day 30 post-inoculation of LBC cells,
70% of Ent. faecalis CECT7121 pre-treated mice survived, whereas no survivals
were recorded in the control group. A group of surviving mice was re-challenged
with LBC cells, and 89% of them survived. Upon stimulation with irradiated
LBC cells, spleen cell proliferation, high IFNc, IL-12 and IL-10 levels
were observed in surviving animals.Ent. faecalis CECT7121 stimulus in a dose-dependent manner,
inducing apoptosis. The production of ceramide was involved in the latter
effect. To undertake in vivo studies, syngeneic BALB ⁄ c mice pre-treated i.p.
with Ent. faecalis CECT7121 (2Æ5 · 108 CFU) were challenged i.p. with LBC
cells (1Æ0 · 106 cells) the day after. On day 30 post-inoculation of LBC cells,
70% of Ent. faecalis CECT7121 pre-treated mice survived, whereas no survivals
were recorded in the control group. A group of surviving mice was re-challenged
with LBC cells, and 89% of them survived. Upon stimulation with irradiated
LBC cells, spleen cell proliferation, high IFNc, IL-12 and IL-10 levels
were observed in surviving animals.in vivo studies, syngeneic BALB ⁄ c mice pre-treated i.p.
with Ent. faecalis CECT7121 (2Æ5 · 108 CFU) were challenged i.p. with LBC
cells (1Æ0 · 106 cells) the day after. On day 30 post-inoculation of LBC cells,
70% of Ent. faecalis CECT7121 pre-treated mice survived, whereas no survivals
were recorded in the control group. A group of surviving mice was re-challenged
with LBC cells, and 89% of them survived. Upon stimulation with irradiated
LBC cells, spleen cell proliferation, high IFNc, IL-12 and IL-10 levels
were observed in surviving animals.Ent. faecalis CECT7121 (2Æ5 · 108 CFU) were challenged i.p. with LBC
cells (1Æ0 · 106 cells) the day after. On day 30 post-inoculation of LBC cells,
70% of Ent. faecalis CECT7121 pre-treated mice survived, whereas no survivals
were recorded in the control group. A group of surviving mice was re-challenged
with LBC cells, and 89% of them survived. Upon stimulation with irradiated
LBC cells, spleen cell proliferation, high IFNc, IL-12 and IL-10 levels
were observed in surviving animals.Æ0 · 106 cells) the day after. On day 30 post-inoculation of LBC cells,
70% of Ent. faecalis CECT7121 pre-treated mice survived, whereas no survivals
were recorded in the control group. A group of surviving mice was re-challenged
with LBC cells, and 89% of them survived. Upon stimulation with irradiated
LBC cells, spleen cell proliferation, high IFNc, IL-12 and IL-10 levels
were observed in surviving animals.Ent. faecalis CECT7121 pre-treated mice survived, whereas no survivals
were recorded in the control group. A group of surviving mice was re-challenged
with LBC cells, and 89% of them survived. Upon stimulation with irradiated
LBC cells, spleen cell proliferation, high IFNc, IL-12 and IL-10 levels
were observed in surviving animals.c, IL-12 and IL-10 levels
were observed in surviving animals.
Conclusions: Enterococcus faecalis CECT7121 affected multiple factors of the
tumour establishment by the following methods: down-regulating the LBC cell
proliferation and inducing apoptosis in these cells; and enhancing the immune
response that protects animals from lymphoma challenge and re-challenge.Enterococcus faecalis CECT7121 affected multiple factors of the
tumour establishment by the following methods: down-regulating the LBC cell
proliferation and inducing apoptosis in these cells; and enhancing the immune
response that protects animals from lymphoma challenge and re-challenge.
Significance and Impact of the Study: This study demonstrate that Ent. faecalisThis study demonstrate that Ent. faecalis
CECT7121 has potential as a probiotic that could facilitate the development of
novel complements to therapeutic strategies against oncological diseases.
Journal of Applied Microbiology ISSN 1364-5072
1234 Journal compilation ª 2010 The Society for Applied Microbiology, Journal of Applied Microbiology 109 (2010) 12341243Journal compilation ª 2010 The Society for Applied Microbiology, Journal of Applied Microbiology 109 (2010) 12341243
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