Pond, Caroline A. and Mattacks, Christine A.
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|DOI (Digital Object Identifier) Link:||http://doi.org/10.1079/BJN2002784|
|Google Scholar:||Look up in Google Scholar|
To explore the hypothesis that proliferating lymphoid cells in immune-stimulated lymph nodes obtain nutrients locally from adjacent adipose tissue, adult guinea-pigs were fed for six weeks on standard chow or on chow supplemented with 10% suet, sunflower oil or fish oil. All ate standard chow for the last five days, during which swelling of one popliteal lymph node was stimulated by repeated local injection of lipopolysaccharide. The fatty acid compositions of phospholipids in both popliteal and in several mesenteric lymph nodes, and of triacylglycerols in 11 samples of adipose tissue defined by their anatomical relations to lymph nodes, were determined by gas chromatography. The proportions of fatty acids in the phospholipids extracted from the stimulated popliteal node correlated best with those of triacylglycerols in the surrounding adipocytes, less strongly with those of adipocytes elsewhere in depots associated with lymphoid tissue, but not with those of nodeless depots. The composition of triacylglycerols in the perinodal adipose tissue may change under local immune stimulation. We conclude that proliferating lymphoid cells in activated lymph nodes obtain fatty acids mainly from the triacylglycerols in adjacent perinodal adipose tissue. Immune stimulation prompts changes in the fatty acid composition of the triacylglycerols of adipocytes in node-containing depots that equip the adipose tissue for provisioning immune responses. Such local interactions show that specialised adipocytes can act as an interface between whole-body and cellular nutrition, and may explain why mammalian adipose tissue is partitioned into a few large and many small depots.
|Item Type:||Journal Article|
|Extra Information:||Copyright held by Cambridge University Press.|
|Keywords:||perinodal adipose tissue; paracrine interactions; adipocyte site-specific properties; popliteal; mesenteric|
|Academic Unit/Department:||Science > Life, Health and Chemical Sciences
|Interdisciplinary Research Centre:||Biomedical Research Network (BRN)|
|Depositing User:||Caroline Pond|
|Date Deposited:||23 Aug 2006|
|Last Modified:||23 Feb 2016 21:15|
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