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缺血再灌注后大鼠回肠和空肠中防御素的含量及定位变化。特定的肽,在特定的位置,执行特定的功能?

Alterations in content and localization of defensins in rat ileum and jejunum following ischemia-reperfusion. Specific peptides, in specific places, for specific jobs?

作者信息

Kozar Rosemary A, Santora Rachel J, Poindexter Brian J, Milner Stephen M, Bick Roger J

出版信息

Eplasty. 2011 Feb 23;11:e8.

PMID:21369366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3044598/
Abstract

OBJECTIVE

To determine alterations in quantities and distributions of natural antimicrobials following ischemia-reperfusion injury. We hypothesized that these compounds would be upregulated in areas of small intestine where changes in permeability and cellular disruption were likely and where protective mechanisms would be initiated.

METHODS

Rats with ischemia-reperfusion underwent superior mesenteric artery clamping and reperfusion. Shams were subjected to laparotomy but no clamping. Ileum and jejunum were harvested and sectioned, and subjected to fluorescence deconvolution microscopy for determinations of content and localization of rat beta defensins, 1, 2, 3; rat neutrophil protein-1; and cathelicidin LL-37. Modeling was performed to determine cellular location of antimicrobials.

RESULTS

Ischemia-reperfusion increased neutrophil defensin alpha (RNP-1) in jejunum; rat beta defensin 1 was increased 2-fold in ileal mucosa and slightly reduced in jejunal mucosa; rat beta defensin 2 was reduced by ischemia-reperfusion in ileum, but slightly increased in jejunum; rat beta defensin 3 was concentrated in the muscularis externa and myenteric plexus of the jejunum; ischemia-reperfusion did not alter cathelicidin LL-37 content in the small intestine, although a greater concentration was seen in jejunum compared with ileum.

CONCLUSION

Ischemia-reperfusion injury caused changes in antimicrobial content in defined areas, and these different regulations might reflect the specific roles of jejunum versus ileum.

摘要

目的

确定缺血再灌注损伤后天然抗菌物质的数量和分布变化。我们假设这些化合物会在小肠中通透性改变和细胞破坏可能发生且保护机制会启动的区域上调。

方法

对大鼠进行肠系膜上动脉夹闭和再灌注以造成缺血再灌注损伤。假手术组仅进行剖腹手术但不夹闭血管。采集回肠和空肠并进行切片,然后通过荧光去卷积显微镜确定大鼠β防御素1、2、3、大鼠中性粒细胞蛋白-1和cathelicidin LL-37的含量及定位。通过建模确定抗菌物质的细胞位置。

结果

缺血再灌注使空肠中的中性粒细胞防御素α(RNP-1)增加;大鼠β防御素1在回肠黏膜中增加了2倍,在空肠黏膜中略有减少;大鼠β防御素2在回肠中因缺血再灌注而减少,但在空肠中略有增加;大鼠β防御素3集中在空肠的外肌层和肌间神经丛;缺血再灌注并未改变小肠中cathelicidin LL-37的含量,尽管空肠中的浓度比回肠中更高。

结论

缺血再灌注损伤导致特定区域抗菌物质含量发生变化,这些不同的调节可能反映了空肠与回肠的特定作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/238f08eb01ab/eplasty11e08_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/fc575a255fca/eplasty11e08_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/bbca8f9c49ec/eplasty11e08_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/005a1c5a4eda/eplasty11e08_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/238f08eb01ab/eplasty11e08_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/fc575a255fca/eplasty11e08_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/bbca8f9c49ec/eplasty11e08_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/005a1c5a4eda/eplasty11e08_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb6/3044598/238f08eb01ab/eplasty11e08_fig4.jpg

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Peptides. 2010 Feb;31(2):195-201. doi: 10.1016/j.peptides.2009.12.008. Epub 2009 Dec 16.
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Enteric defensins are essential regulators of intestinal microbial ecology.肠防御素是肠道微生物生态的重要调节因子。
Nat Immunol. 2010 Jan;11(1):76-83. doi: 10.1038/ni.1825. Epub 2009 Oct 22.
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Human defensins and LL-37 in mucosal immunity.黏膜免疫中的人防御素和 LL-37。
J Leukoc Biol. 2010 Jan;87(1):79-92. doi: 10.1189/jlb.0609382. Epub 2009 Oct 6.
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Intestinal ischemic preconditioning after ischemia/reperfusion injury in rat intestine: profiling global gene expression patterns.肠缺血预处理对大鼠肠缺血/再灌注损伤的作用:全基因表达谱分析。
Dig Dis Sci. 2010 Jul;55(7):1866-77. doi: 10.1007/s10620-009-0980-4. Epub 2009 Sep 25.
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Selective reciprocity in antimicrobial activity versus cytotoxicity of hBD-2 and crotamine.人β-防御素2(hBD-2)和巴胺在抗菌活性与细胞毒性方面的选择性相互作用。
Proc Natl Acad Sci U S A. 2009 Sep 1;106(35):14972-7. doi: 10.1073/pnas.0904465106. Epub 2009 Aug 13.
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Defensins are differentially expressed with respect to the anatomic region in the upper gastrointestinal tract of children.防御素在儿童上消化道的不同解剖区域存在差异表达。
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