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免疫抑制进行性阶段大鼠器官中潜伏性卡氏肺孢子虫的增殖模式。

Proliferation patterns of latent Pneumocystis carinii in rat organs during progressive stages of immunosuppression.

作者信息

Reddy L V, Zammit C

机构信息

Center for Molecular Biology, MCHT, Wayne State University, Detroit, MI 48201.

出版信息

J Protozool. 1991 Nov-Dec;38(6):43S-47S.

PMID:1824564
Abstract

Pneumocystis carinii is known to proliferate mainly in the lung of an immunocompromised host. In AIDS and other immune disorders sporadic extrapulmonary presence of this organism has been documented. Occasionally, P. carinii does not appear to infect the lung. These observations have been based on the detection of P. carinii by conventional staining techniques. We have sought to determine the extent of these infections by the polymerase chain reaction (PCR) in a rat model. Harlan Sprague-Dawley rats weighing between 110 and 130 g were immunosuppressed with dexamethasone (1.2 mg/l) in drinking water. During progressive stages of immunosuppression 2 rats were sacrificed at 2, 3, 4 and 5 wk, and the lung, liver, kidney, spleen and bone marrow were taken. Sonicated crude extracts of the tissues were used as template DNA for the amplification of the dihydrofolate reductase (DHFR) gene of P. carinii. All the PCR products were analyzed by Southern hybridization with radiolabelled DHFR DNA. These analyses revealed a general trend of P. carinii proliferation first in bone marrow at 2 wk, followed by liver at 3 wk, and lung at 5 wk on immunosuppression. Kidney and spleen infections were infrequent. Although P. carinii appears to proliferate in the lung at later stages of immunosuppression, the degree of proliferation is several-fold greater than in extrapulmonary organs. The extrapulmonary proliferation of P. carinii, however small, may possibly suppress hematopoietic stem cell differentiation in bone marrow, and may also contribute to the pathology present in various organs.

摘要

已知卡氏肺孢子虫主要在免疫功能低下宿主的肺部增殖。在艾滋病和其他免疫紊乱疾病中,已记录到该病原体偶尔会在肺外出现。偶尔,卡氏肺孢子虫似乎不会感染肺部。这些观察结果基于通过传统染色技术检测卡氏肺孢子虫。我们试图通过聚合酶链反应(PCR)在大鼠模型中确定这些感染的程度。选用体重在110至130克之间的Harlan Sprague-Dawley大鼠,通过在饮用水中添加地塞米松(1.2毫克/升)进行免疫抑制。在免疫抑制的进展阶段,分别在第2、3、4和5周处死2只大鼠,并取其肺、肝、肾、脾和骨髓。将组织的超声破碎粗提物用作模板DNA,用于扩增卡氏肺孢子虫的二氢叶酸还原酶(DHFR)基因。所有PCR产物通过与放射性标记的DHFR DNA进行Southern杂交分析。这些分析显示,在免疫抑制状态下,卡氏肺孢子虫首先在第2周于骨髓中增殖,随后在第3周于肝脏中增殖,第5周于肺部增殖。肾脏和脾脏感染较少见。虽然卡氏肺孢子虫似乎在免疫抑制后期在肺部增殖,但其增殖程度比肺外器官高几倍。然而,卡氏肺孢子虫在肺外的增殖,无论多么微小,都可能抑制骨髓中的造血干细胞分化,也可能导致各器官出现病变。

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