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suck abstract from ncbi


10.1152/ajprenal.00532.2014

http://scihub22266oqcxt.onion/10.1152/ajprenal.00532.2014
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25673809!ä!25673809

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suck abstract from ncbi

pmid25673809      Am+J+Physiol+Renal+Physiol 2015 ; 308 (9): F956-66
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  • A microscopic view on the renal endothelial glycocalyx #MMPMID25673809
  • Dane MJ; van den Berg BM; Lee DH; Boels MG; Tiemeier GL; Avramut MC; van Zonneveld AJ; van der Vlag J; Vink H; Rabelink TJ
  • Am J Physiol Renal Physiol 2015[May]; 308 (9): F956-66 PMID25673809show ga
  • Endothelial cells perform key homeostatic functions such as regulating blood flow, permeability, and aiding immune surveillance for pathogens. While endothelial activation serves normal physiological adaptation, maladaptation of these endothelial functions has been identified as an important effector mechanism in the progression of renal disease as well as the associated development of cardiovascular disease. The primary interface between blood and the endothelium is the glycocalyx. This carbohydrate-rich gel-like structure with its associated proteins mediates most of the regulatory functions of the endothelium. Because the endothelial glycocalyx is a highly dynamic and fragile structure ex vivo, and traditional tissue processing for staining and perfusion-fixation usually results in a partial or complete loss of the glycocalyx, studying its dimensions and function has proven to be challenging. In this review, we will outline the core functions of the glycocalyx and focus on different techniques to study structure-function relationships in kidney and vasculature.
  • |*Microscopy/methods[MESH]
  • |Animals[MESH]
  • |Endothelial Cells/metabolism/*ultrastructure[MESH]
  • |Glycocalyx/metabolism/*ultrastructure[MESH]
  • |Humans[MESH]
  • |Kidney Diseases/metabolism/*pathology/physiopathology[MESH]
  • |Kidney/*blood supply[MESH]
  • |Specimen Handling[MESH]


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