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用白细胞介素1(IL-1)预处理的受辐照小鼠中造血集落形成细胞的恢复情况。

Recovery of hematopoietic colony-forming cells in irradiated mice pretreated with interleukin 1 (IL-1).

作者信息

Schwartz G N, Neta R, Vigneulle R M, Patchen M L, MacVittie T J

机构信息

Experimental Hematology Department, Armed Forces Radiobiology Research Institute, Bethesda, Maryland.

出版信息

Exp Hematol. 1988 Oct;16(9):752-7.

PMID:3262530
Abstract

Data in this report determined the effect of a single injection of recombinant interleukin 1 alpha (rIL-1) prior to irradiation of B6D2F1 mice on the recovery of colony-forming cells (CFC) at early and late times after sublethal and lethal doses of radiation. Injection of rIL-1 promoted an earlier recovery of mature cells in the blood and CFC in the bone marrow and spleen. For example, 8 days after 6.5 Gy irradiation, the number of CFU-E (colony-forming units-erythroid), BFU-E (burst-forming units-erythroid), and GM-CFC (granulocyte-macrophage colony-forming cells) per femur was approximately 1.5-fold higher in rIL-1-injected mice than in saline-injected mice. Also, 5, 9, and 12 days after irradiation, the number of both day 8 and day 12 CFU-S (colony-forming units-spleen) was almost twofold greater in bone marrow from rIL-1-injected mice. The earlier recovery of CFU-S in rIL-1-injected mice was not associated with an increase in the number of CFU-S that survived immediately after irradiation. Also, 7 months after irradiation, the number of CFU-S per femur of both saline- and rIL-1-injected mice was still less than 50% of normal values. Data in this report demonstrate that a single injection of rIL-1 prior to irradiation accelerates early hematopoietic recovery in irradiated mice, but does not prevent expression of radiation-induced frontend damage or long-term damage to hematopoietic tissues.

摘要

本报告中的数据确定了在对B6D2F1小鼠进行辐射之前单次注射重组白细胞介素1α(rIL-1)对亚致死剂量和致死剂量辐射后早期和晚期集落形成细胞(CFC)恢复的影响。注射rIL-1促进了血液中成熟细胞以及骨髓和脾脏中CFC的更早恢复。例如,在6.5 Gy辐射后8天,注射rIL-1的小鼠每根股骨的CFU-E(红细胞集落形成单位)、BFU-E(红细胞爆式集落形成单位)和GM-CFC(粒细胞-巨噬细胞集落形成细胞)数量比注射生理盐水的小鼠高出约1.5倍。此外,在辐射后5天、9天和12天,注射rIL-1的小鼠骨髓中第8天和第12天的CFU-S(脾集落形成单位)数量几乎是其两倍。注射rIL-1的小鼠中CFU-S的更早恢复与辐射后立即存活的CFU-S数量增加无关。而且,在辐射后7个月,注射生理盐水和rIL-1的小鼠每根股骨的CFU-S数量仍低于正常值的50%。本报告中的数据表明,在辐射前单次注射rIL-1可加速受辐射小鼠的早期造血恢复,但不能预防辐射诱导的前端损伤或造血组织的长期损伤的表达。

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