Dual roles of modulatory calcineurin-interacting protein 1 in cardiac hypertrophy.

Abstract

The calcium/calmodulin-dependent protein phosphatase calcineurin stimulates cardiac hypertrophy in response to numerous stimuli. Calcineurin activity is suppressed by association with modulatory calcineurin-interacting protein (MCIP)1DSCR1, which is up-regulated by calcineurin signaling and has been proposed to function in a negative feedback loop to modulate calcineurin activity. To investigate the involvement of MCIP1 in cardiac hypertrophy in vivo, we generated MCIP1 null mice and subjected them to a variety of stress stimuli that induce cardiac hypertrophy. In the absence of stress, MCIP1(-/-) animals exhibited no overt phenotype. However, the lack of MCIP1 exacerbated the hypertrophic response to activated calcineurin expressed from a muscle-specific transgene, consistent with a role of MCIP1 as a negative regulator of calcineurin signaling. Paradoxically, however, cardiac hypertrophy in response to pressure overload or chronic adrenergic stimulation was blunted in MCIP1(-/-) mice. These findings suggest that MCIP1 can facilitate or suppress cardiac calcineurin signaling depending on the nature of the hypertrophic stimulus. These opposing roles of MCIP have important implications for therapeutic strategies to regulate cardiac hypertrophy through modulation of calcineurin-MCIP activity.

• Authors: Rick B Vega, Beverly A Rothermel, Carla J Weinheimer, Atilla Kovacs, R H Naseem, Rhonda Bassel-Duby, R S Williams, Eric N Olson
• Journal: Proceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 100 Issue 2 Pg. 669-74 (Jan 21 2003) ISSN: 0027-8424 [Print] United States
• PMID: 12515860 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• DNA-Binding Proteins
• Intracellular Signaling Peptides and Proteins
• Muscle Proteins
• RCAN1 protein, human
• Calcineurin

Topics

• Animals
• Calcineurin (analysis, physiology)
• Cardiomegaly (etiology)
• DNA-Binding Proteins
• Intracellular Signaling Peptides and Proteins
• Male
• Mice
• Mice, Knockout
• Muscle Proteins (physiology)