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Activation of smooth muscle and myenteric plexus cells of jejunum via toll-like receptor 4

✍ Scribed by Cristiano Rumio; Dario Besusso; Francesca Arnaboldi; Marco Palazzo; Silvia Selleri; Silvia Gariboldi; Shizuo Akira; Satoshi Uematsu; Paola Bignami; Valerio Ceriani; Sylvie Ménard; Andrea Balsari


Book ID
102882547
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
583 KB
Volume
208
Category
Article
ISSN
0021-9541

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✦ Synopsis


Abstract

The cell types of the gut expressing Toll‐like receptor 4, which recognizes specifically bacterial lipopolysaccharides, as well as the functionality of this receptor, have remained controversial. We aimed to clarify these issues. Mouse and human intestinal specimens were stained immunohistochemically to detect Toll‐like receptor 4 expression. Smooth muscle and myenteric plexus cells but not enterocytes revealed receptor expression. Murine intestinal smooth muscle and myenteric plexus cells but not enterocytes showed nuclear translocation of nuclear factor‐kappaB after in vivo stimulation with lipopolysaccharide. Moreover, lipopolysaccharide added to human jejunum biopsies free of epithelial cells induced release of interleukin‐8 (IL‐8). We can conclude that Toll‐like receptor 4 is not expressed in epithelial layer, but rather on smooth muscle and myenteric plexus cells and that expression is functional. The expression of Toll‐like receptor 4 on smooth muscle and myenteric plexus cells is consistent with the possibility that these cells are involved in intestinal immune defense; the low or absent expression of Toll‐like receptor 4 on enterocytes might explain the intestinal epithelium hyporesponsiveness to the abundance of LPS in the intestinal lumen. J. Cell. Physiol. © 2006 Wiley‐Liss, Inc.


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## Abstract Endotoxemia by bacterial lipopolysaccharide (LPS) has been reported to affect gut motility specifically depending on Toll‐like receptor 4 activation (TLR4). However, the direct impact of LPS ligation to TLR4 on human smooth muscle cells (HSMC) activity still remains to be elucidated. Th