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Canada Only. So it is plausible to postulate that the pathways coupled to the AT 2 receptor depend on the cell type and even the localization of these cells in the kidney. This hypothesis is supported by the observation that several pathways have been described to be coupled to the AT 2 receptor in the same or in different cell types [ 18 , 32 ].
Further experiments will be necessary to clarify this issue. All of the results of the present study were obtained using basolateral membranes isolated from proximal tubule cells. Several components of different cell signalling pathways are present in the basolateral membrane, including G-proteins, phospholipases and protein kinases [ 5 , 6 , 12 ]. In general, it is accepted that the activation of the kinases involves the redistribution of enzymes from cytosol to membrane.
However, Chakravarthy et al. In previous studies, we showed that the isolated basolateral membranes of renal proximal tubules contain a constitutive PKC and PKA that, when activated by phorbol ester or cAMP respectively, phosphorylate other proteins located in this membrane [ 40 , 44 ]. This result agrees with the observation that guanylate cyclase is present in the plasma membranes of different cell types [ 46 ].
In the present study, we have shown that isolated basolateral membranes of outer renal proximal tubules contain a constitutive PKG that is stimulated by cGMP. The presence of complete signalling complexes in plasma membrane, from receptors to all intermediary elements, to final membrane targets, illustrates an important means by which fine and fast modulation of renal sodium reabsorption by proximal tubule cells during acute sodium intake changes can occur.
This hypothesis is in agreement with the proposal that cellular signalling could occur in distinct components or even in microdomains of the plasma membrane such as caveolae. Such compartmentalization is usually associated with epithelial cell types, such as kidney cells [ 47 ].
Read article at publisher's site DOI : Hypertension , 77 6 , 12 Apr Patel S , Hussain T. Pharmacol Res Perspect , 8 6 :e, 01 Dec Physiol Rep , 7 5 :e, 01 Mar Curr Hypertens Rep , 20 5 , 01 May Review Free to read. Physiol Rev , 98 1 , 01 Jan This data has been text mined from the article, or deposited into data resources.
To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation. Regul Pept , , 01 Aug Cited by: 48 articles PMID: Peptides , 31 5 , 03 Mar Cited by: 9 articles PMID: Exp Physiol , 93 5 , 01 Feb Cited by: 21 articles PMID: Biomed Res Int , , 17 Oct Carey RM. Curr Hypertens Rep , 19 3 , 01 Mar Contact us. Europe PMC requires Javascript to function effectively.
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Caruso-Neves C. Affiliations 1 author 1. Share this article Share with email Share with twitter Share with linkedin Share with facebook. Abstract The molecular mechanisms involved in the Ang- [angiotensin- ] effect on sodium renal excretion remain to be determined.
In this condition, Ang- at 0. Ang- at 0. Free full text. Biochem J. Published online Mar Prepublished online Jan 4. PMID: Author information Article notes Copyright and License information Disclaimer.
Copyright The Biochemical Society, London. This article has been cited by other articles in PMC. Go to:. Preparation of isolated basolateral membranes The basolateral membranes of the outer cortex were prepared from adult pig kidneys. Immunoblotting The presence in basolateral membranes of PKG and AT 2 receptor protein was determined by immunoblotting. Open in a separate window. Figure 1. Figure 2. Figure 3. Figure 4. Figure 5. Figure 6. Figure 7.
Kucharewicz I. Angiotensin- 1—7 : an active member of the renin—angiotensin system J. Handa R.
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