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胎儿接受伽马射线照射会损害正在发育的造血微环境,而非造血祖细胞。

Gamma irradiation of the fetus damages the developing hemopoietic microenvironment rather than the hemopoietic progenitor cells.

作者信息

Yang F T, Lord B I, Hendry J H

机构信息

CRC Department of Experimental Haematology, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, England.

出版信息

Radiat Res. 1995 Mar;141(3):309-13.

PMID:7871158
Abstract

Hemopoiesis is the product of two components: the hemopoietic tissue and the regulatory stromal microenvironment in which it resides. Plutonium-239, incorporated during fetal development, is known to cause deficient hemopoiesis. A predetermined equivalent gamma-ray dose has now been used in combination with cross-transplantation experiments to separate these two components and define where the damage arises. It was confirmed that 1.8 Gy gamma irradiation at midterm gestation caused a 40% reduction in the hemopoietic stem (spleen colony-forming) cell population of their offspring which persisted to at least 24 weeks of age. Spleen colony formation after sublethal doses of gamma rays reflected this reduced complement of endogenous stem cells. The regulatory hemopoietic microenvironment, measured as fibroblastoid colony-forming cells, was similarly depleted. Normal growth of the CFU-S population after transplantation into standard recipients showed that the quality of the stem cell population in the offspring of irradiated mothers was not affected. By contrast, when used as recipients of a bone marrow transplant from either normal or irradiated offspring, the offspring of irradiated mothers were unable to support normal growth: there was a twofold difference in the number of CFU-S per femur for at least 100 days after transplantation. There were 70% fewer CFU-F in the femur 1 month after bone marrow transplantation when the offspring of irradiated mothers were used as transplant recipients compared to when normal offspring were used. This not only confirmed their reduced capacity to host normal stem cells but also indicated that CFU-F in the transplant were unable to compensate for the poor microenvironment in the irradiated offspring hosts. It is concluded that irradiation at midterm gestation damages the developing regulatory microenvironment but not the hemopoietic stem cell population that it hosts.

摘要

造血作用是两种成分的产物

造血组织及其所驻留的调节性基质微环境。已知在胎儿发育期间摄入的钚-239会导致造血作用不足。现在,已将预先确定的等效γ射线剂量与交叉移植实验相结合,以分离这两种成分并确定损伤发生的位置。已证实,妊娠中期进行1.8 Gy的γ射线照射会使其后代的造血干细胞(脾集落形成细胞)数量减少40%,这种情况至少持续到24周龄。亚致死剂量γ射线照射后的脾集落形成反映了内源性干细胞数量的减少。以成纤维细胞样集落形成细胞衡量的调节性造血微环境也同样减少。移植到标准受体后CFU-S群体的正常生长表明,受照射母亲后代的干细胞群体质量未受影响。相比之下,当作为来自正常或受照射后代的骨髓移植受体时,受照射母亲的后代无法支持正常生长:移植后至少100天,每根股骨的CFU-S数量存在两倍的差异。与使用正常后代作为移植受体相比,当使用受照射母亲的后代作为移植受体时,骨髓移植1个月后股骨中的CFU-F减少了70%。这不仅证实了它们容纳正常干细胞的能力降低,还表明移植中的CFU-F无法弥补受照射后代宿主中不良的微环境。结论是,妊娠中期照射会损害发育中的调节性微环境,但不会损害其容纳的造血干细胞群体。

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