Key result
Ectodomain shedding of angiotensin-converting enzyme (ACE) plays a critical role in regulating tissue ACE levels, and targeting this process may offer novel therapeutic approaches for cardiovascular diseases.
Understanding the proteolytic shedding of ACE and its genetic variants offers novel therapeutic avenues for regulating tissue ACE levels in cardiovascular diseases.
A number of membrane proteins are enzymatically cleaved or 'shed' from the cell surface, resulting in the modulation of biological events and opening novel pharmaceutical approaches to diverse diseases by targeting shedding. Our focus has been on understanding the shedding of angiotensin-converting enzyme (ACE), an enzyme that plays a pivotal role in blood pressure regulation. The identification of novel hereditary ACE mutations that result in increased ACE shedding has advanced our understanding of the role of ACE shedding in health and disease. Extensive biochemical and molecular analysis has helped to elucidate the mechanism of ACE shedding. These findings point to the potential therapeutic role of targeting shedding in regulating tissue ACE levels in cardiovascular disease.
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Ehlers et al. (2012) conducted a review in Hypertension and Cardiovascular Disease. Ectodomain shedding of angiotensin-converting enzyme (ACE) plays a critical role in regulating tissue ACE levels, and targeting this process may offer novel therapeutic approaches for cardiovascular diseases.
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