Key result
During the differentiation of murine 3T3-L1 preadipocytes, AT1 receptors were detected throughout, whereas the strong AT2 signal in preadipocytes was completely lost.
In murine 3T3-L1 preadipocytes, AT2 receptor expression is inversely correlated with adipose differentiation, whereas AT1 expression is maintained.
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AT2 loss during murine preadipocyte differentiation should not change practice; leaves open its role in human adipogenesis or cardiometabolic risk.
During their development from progenitor cells, adipocytes not only express enzymatic activities necessary for the storage of triglycerides, but also achieve the capability to produce a number of endocrine factors such as leptin, tumor necrosis factor alpha (TNFalpha), complement factors, adiponectin/adipoQ, plasminogen activator inhibitor-1 (PAI-1), angiotensin II and others. Angiotensin II is produced from angiotensinogen by the proteolytic action of renin and angiotensin-converting enzyme; and several data point to the existence of a complete local renin-angiotensin system in adipose tissue, including angiotensin II receptors. In this study, we directly monitored the production of angiotensin II type one receptor (AT1) and angiotensin II type two receptor (AT2) proteins during the adipose conversion of murine 3T3-L1 preadipocytes by immunodetection with specific antibodies. AT1 receptors could be detected throughout the whole differentiation period. The strong AT2 signal in preadipocytes however was completely lost during the course of differentiation, which suggests that expression of AT2 receptors is inversely correlated to the adipose conversion program.
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Mallow et al. (2000) studied Adipose conversion. Adipose conversion of murine 3T3-L1 preadipocytes was evaluated on Production of AT1 and AT2 receptor proteins. During the differentiation of murine 3T3-L1 preadipocytes, AT1 receptors were detected throughout, whereas the strong AT2 signal in preadipocytes was completely lost.
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