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单次注射关节炎支原体后小鼠造血干细胞的增殖与脾脏迁移

[Proliferation and splenic migration of mouse hematopoietic stem cells following a single injection of Mycoplasma arthritidis].

作者信息

Sanin A V

出版信息

Biull Eksp Biol Med. 1986 Jul;102(7):89-92.

PMID:3730601
Abstract

The effect of a single injection of live M. arthritidis microorganisms on the bone marrow and spleen CFU-S populations was assessed. One of the principal findings is that marrow CFU-S are recruited into cell cycle (as determined by hydroxyurea kill) early after M. arthritidis administration and stay in the cycle for at least 2 weeks thereafter. The peak level of cycling value (47%) was observed on day 4. The duration of increased CFU-S cycling activity was shown to coincide with a time period during which a significant rise in the number of endogenous CFU-S was maintained. The other important finding is that splenic seeding efficiency ("f-factor") declines by 56% one day following M. arthritidis administration. The latter effect could be attributed to the binding of mycoplasmas to the surface of CFU-S as specific rabbit antiserum against M. arthritidis incubated in vitro with the bone marrow cells of infected donor mice caused an up to 48% reduction in the in vivo colony-forming ability of CFU-S.

摘要

评估了单次注射活关节炎支原体微生物对骨髓和脾脏CFU-S群体的影响。一个主要发现是,在给予关节炎支原体后早期,骨髓CFU-S被募集进入细胞周期(通过羟基脲杀伤确定),并在此后至少2周内保持在细胞周期中。在第4天观察到循环值的峰值水平(47%)。CFU-S循环活性增加的持续时间与内源性CFU-S数量显著增加的时间段一致。另一个重要发现是,在给予关节炎支原体一天后,脾脏接种效率(“f因子”)下降了56%。后一种效应可能归因于支原体与CFU-S表面的结合,因为用感染供体小鼠的骨髓细胞在体外孵育的抗关节炎支原体特异性兔抗血清可使CFU-S的体内集落形成能力降低多达48%。

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