Migliore-Samour D, Bousseau A, Caillaud J M, Naussac A, Sedqi M, Ferradini C, Jollès P
Laboratoire des protéines, CNRS URA 1188, Université de Paris V, France.
Experientia. 1993 Feb 15;49(2):160-6. doi: 10.1007/BF01989422.
The lipopeptide lauroyl-L-Ala-gamma-D-Glu-L,L-A2pm (LtriP) increased the resistance of mice to the lethal effect of gamma-ray irradiation. The radioprotective effect was dependent on the doses of LtriP and of radiation. Maximum survival was observed when the lipopeptide was injected on two successive days before irradiation. This activity seems to be related to immunostimulating functions, since the non-immunostimulating analog lauroyl-L-Ala-gamma-D-Glu-D,D-A2pm-Gly, containing D,D-diaminopimelic acid, was not radioprotective. The protective activity might result from an induction of cytokines, such as IL-1, TNF and M-CSF, since LtriP induced the mRNA expression and the secretion of these immunomodulators.
脂肽月桂酰-L-丙氨酸-γ-D-谷氨酸-L,L-二氨基庚二酸(LtriP)增强了小鼠对γ射线辐射致死效应的抵抗力。辐射防护作用取决于LtriP的剂量和辐射剂量。当在辐射前连续两天注射脂肽时,观察到最大存活率。这种活性似乎与免疫刺激功能有关,因为含有D,D-二氨基庚二酸的非免疫刺激类似物月桂酰-L-丙氨酸-γ-D-谷氨酸-D,D-二氨基庚二酸-甘氨酸没有辐射防护作用。保护活性可能是由细胞因子如白细胞介素-1、肿瘤坏死因子和巨噬细胞集落刺激因子的诱导所致,因为LtriP诱导了这些免疫调节剂的mRNA表达和分泌。