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感染大肠杆菌的新生小鼠未能加速中性粒细胞生成,这与其未能增加粒细胞集落刺激因子和白细胞介素-6的转录本有关。

The failure of newborn mice infected with Escherichia coli to accelerate neutrophil production correlates with their failure to increase transcripts for granulocyte colony-stimulating factor and interleukin-6.

作者信息

Liechty K W, Schibler K R, Ohls R K, Perkins S L, Christensen R D

机构信息

Division of Human Development and Aging, University of Utah School of Medicine, Salt Lake City.

出版信息

Biol Neonate. 1993;64(5):331-40. doi: 10.1159/000244007.

Abstract

We quantified circulating and storage neutrophils, their precursors and progenitors, and mRNA for some of the cytokines involved in granulocytopoiesis, in newborn and adult mice following intrapulmonary inoculation of Escherichia coli. Four hours following inoculation of adult and newborn mice with a quantity of organisms 2 logs below the LD100, all animals were neutropenic. After 24 h, adults had recovered from the neutropenia but neonates had not (p < 0.001). Accelerated neutrophil production was evident in the infected adults, and correlated with the appearance of granulocyte colony-stimulating factor (G-CSF) transcripts in the liver, spleen, and lung, and interleukin-6 (IL-6) transcripts in the spleen and lung. An increase in neutrophil production was not observed in the neonates, and none of their organs tested had transcripts for either G-CSF or IL-6, but they did have transcripts for cytokines not involved in granulocytopoiesis; macrophage colony-stimulating factor and its receptor (c-fms). We speculate that the failure to increase neutrophil production in infected neonatal mice is the result of failure to increase production of relevant cytokines.

摘要

在新生小鼠和成年小鼠经肺内接种大肠杆菌后,我们对循环和储存的中性粒细胞、其前体和祖细胞以及一些参与粒细胞生成的细胞因子的mRNA进行了定量分析。在用低于半数致死量(LD100)2个对数的菌量接种成年和新生小鼠4小时后,所有动物均出现中性粒细胞减少。24小时后,成年小鼠从中性粒细胞减少中恢复,但新生小鼠未恢复(p < 0.001)。受感染的成年小鼠中中性粒细胞生成加速明显,且与肝脏、脾脏和肺中粒细胞集落刺激因子(G-CSF)转录本以及脾脏和肺中白细胞介素-6(IL-6)转录本的出现相关。新生小鼠未观察到中性粒细胞生成增加,其检测的任何器官均无G-CSF或IL-6的转录本,但它们确实有不参与粒细胞生成的细胞因子的转录本;巨噬细胞集落刺激因子及其受体(c-fms)。我们推测,受感染的新生小鼠中性粒细胞生成未能增加是相关细胞因子生成未能增加的结果。

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