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Peptide receptors in astroglia: Focus on angiotensin II and atrial natriuretic peptide

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AbstractAstroglial cells derived from the mammalian central nervous system contain a wide variety of peptide receptors, including specific sites for angiotensin II (AII) and atrial natriuretic peptide (ANP). The AII receptors present in these cells are primarily of the AT1 subtype. The ANP receptors present in these cells consist of a mix of ANP‐A and ANP‐B sites (“biological receptors”) and also ANP‐C sites (“clearance receptors”). Available evidence indicates that activation of AII receptors results in a stimulation of astroglial proliferation, whereas ANP has an antiproliferative effect in these cells. Intracellular pathways which may mediate these effects of AII and ANP on cell proliferation are discussed, including the presentation of novel data on the activation of protein kinase C and of glucose uptake by AII. We also consider the possibility that the opposing actions of AII and ANP on astroglial proliferation may represent another facet of the mutual antagonism between these two peptides, which has been observed throughout mammalian systems. © 1994 Wiley‐Liss, Inc.
Title: Peptide receptors in astroglia: Focus on angiotensin II and atrial natriuretic peptide
Description:
AbstractAstroglial cells derived from the mammalian central nervous system contain a wide variety of peptide receptors, including specific sites for angiotensin II (AII) and atrial natriuretic peptide (ANP).
The AII receptors present in these cells are primarily of the AT1 subtype.
The ANP receptors present in these cells consist of a mix of ANP‐A and ANP‐B sites (“biological receptors”) and also ANP‐C sites (“clearance receptors”).
Available evidence indicates that activation of AII receptors results in a stimulation of astroglial proliferation, whereas ANP has an antiproliferative effect in these cells.
Intracellular pathways which may mediate these effects of AII and ANP on cell proliferation are discussed, including the presentation of novel data on the activation of protein kinase C and of glucose uptake by AII.
We also consider the possibility that the opposing actions of AII and ANP on astroglial proliferation may represent another facet of the mutual antagonism between these two peptides, which has been observed throughout mammalian systems.
© 1994 Wiley‐Liss, Inc.

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