Caspase inhibition increases survival of neural stem cells in the gastrointestinal tract

被引:33
作者
Micci, MA [1 ]
Pattillo, MT [1 ]
Kahrig, KM [1 ]
Pasricha, PJ [1 ]
机构
[1] Univ Texas, Med Branch, Div Gastroenterol & Hepatol, Enter Neuromuscular Disorders & Pain Lab, Galveston, TX 77555 USA
关键词
apoptosis; caspase-1; inhibitor; cyclosporin; enteric nervous system; neural stem cells; pylorus;
D O I
10.1111/j.1365-2982.2005.00702.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Neural stem cell (NSC) transplantation is a promising tool for the restoration of the enteric nervous system in a variety of motility disorders. Post-transplant survival represents a critical limiting factor for successful repopulation. The aim of this study was to determine the role of both immunological as well as non-immune-mediated mechanisms on post-transplant survival of NSC in the gut. Mouse CNS-derived NSC (CNS-NSC) were transplanted into the pylorus of recipient mice with and without the addition of a caspase-1 inhibitor (Ac-YVAD-cmk) in the injection media. In a separate experiment, CNS-NSC were transplanted in the pylorus of mice that were immunosuppressed by administration of cyclosporin A (CsA). Apoptosis and proliferation of the implanted cells was assessed 1 and 7 days post-transplantation. Survival was assessed 1 week post-transplantation. The degree of immunoresponse was also measured. The addition of a caspase-1 inhibitor significantly reduced apoptosis, increased proliferation and enhanced survival of CNS-NSC. CsA-treatment did not result in improved survival. Our results indicate that caspase-1 inhibition, but not immunosuppression, improves survival of CNS-NSC in the gut. Pre-treatment with a caspase-1 inhibitor may be a practical method to enhance the ability of transplanted CNS-NSC to survive in their new environment.
引用
收藏
页码:557 / 564
页数:8
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