Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic Injury

被引:17
作者
Rodriguez-Barrera, Roxana [1 ,2 ,3 ,4 ]
Fernandez-Presas, Ana M. [5 ]
Garcia, Elisa [1 ,3 ]
Flores-Romero, Adrian [1 ,3 ]
Martinon, Susana [1 ,3 ]
Yazmin Gonzalez-Puertos, Viridiana [2 ]
Mestre, Humberto [1 ]
Flores-Dominguez, Carmina [1 ]
Rodriguez-Mata, Veronica [5 ]
Koenigsberg, Mina [2 ]
Solano, Sandra [5 ]
Ibarra, Antonio [1 ,3 ]
机构
[1] Univ Anahuac Mexico Norte, Fac Ciencias Salud, Edo De Mexico 52786, Mexico
[2] Univ Autonoma Metropolitana Iztapalapa, Div Ciencias Biol & Salud, Dept Ciencias Salud, Mexico City 09340, DF, Mexico
[3] Ctr Invest Proyecto CAMINA AC, Mexico City 14050, DF, Mexico
[4] Univ Autonoma Metropolitana Iztapalapa, Mexico City 09340, DF, Mexico
[5] Univ Nacl Autonoma Mexico, Fac Med, Dept Microbiol & Parasitol, Mexico City 04510, DF, Mexico
关键词
NECROSIS-FACTOR-ALPHA; NITRIC-OXIDE; NEUROTROPHIC FACTOR; GLIAL APOPTOSIS; T-CELLS; NEURONS; IMMUNE; AUTOIMMUNITY; VACCINATION; EXPRESSION;
D O I
10.1155/2013/827517
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Apoptosis is one of the most destructive mechanisms that develop after spinal cord (SC) injury. Immunization with neural-derived peptides (INDPs) such as A91 has shown to reduce the deleterious proinflammatory response and the amount of harmful compounds produced after SC injury. With the notion that the aforementioned elements are apoptotic inducers, we hypothesized that INDPs would reduce apoptosis after SC injury. In order to test this assumption, adult rats were subjected to SC contusion and immunized either with A91 or phosphate buffered saline (PBS; control group). Seven days after injury, animals were euthanized to evaluate the number of apoptotic cells at the injury site. Apoptosis was evaluated using DAPI and TUNEL techniques; caspase-3 activity was also evaluated. To further elucidate the mechanisms through which A91 exerts this antiapoptotic effects we quantified tumor necrosis factor-alpha (TNF-alpha). To also demonstrate that the decrease in apoptotic cells correlated with a functional improvement, locomotor recovery was evaluated. Immunization with A91 significantly reduced the number of apoptotic cells and decreased caspase-3 activity and TNF-alpha concentration. Immunization with A91 also improved the functional recovery of injured rats. The present study shows the beneficial effect of INDPs on preventing apoptosis and provides more evidence on the neuroprotective mechanisms exerted by this strategy.
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页数:8
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