Key result
Permanent ANP removal in mice increases GC-A and GC-B mRNA and lowers C-receptor mRNA.
Permanent removal of ANP from the natriuretic peptide system results in up-regulation of GC-A and GC-B and down-regulation of C-receptor in the lung, which may contribute to chronic hypertension and cardiac hypertrophy.
ANP loss alters receptor expression in mice; leaves open whether similar compensation drives human hypertension or hypertrophy.
BACKGROUND: The atrial natriuretic peptide (ANP) family is a complex system consisting of at least three polypeptides and at least three types of receptor. Each peptide interacts with different types of receptor at varying degrees of affinity. To determine if natriuretic peptide levels influence natriuretic peptide receptor expression and regulation, we examined the expression of guanylyl cyclase linked GC-A, GC-B and C-receptor in the lungs of mice with a mutation that inactivates the ANP gene (Nppa). METHODS: The mRNA level of GC-A, GC-B and C-receptor in the lung were studied by ribonuclease protection assays (RPA). RESULTS: Results of RPA showed that although the mRNA level of GC-A and GC-B of heterozygous ANP+/- was not different from wild type ANP+/+ mice, they were significantly higher in the homozygous mutant ANP-/- mice. In addition, C-receptor mRNA level in ANP+/- and ANP-/- was significantly lower than ANP+/+ mice. The C-receptor results were confirmed by receptor binding assays and affinity cross-linking studies. CONCLUSIONS: Taken together these data suggest that permanent removal of ANP from the natriuretic peptide system results in an up-regulation of GC-A and GC-B, and a corresponding down-regulation of C-receptor in the lung of proANP gene disrupted mice. We postulated that changes in the natriuretic peptide receptor population may result in chronic hypertension and cardiac hypertrophy in the ANP-/- mice.
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N Vera (2000) studied proANP gene disruption. ANP gene disruption (Nppa mutation) vs. Wild type ANP+/+ mice was evaluated on mRNA level of GC-A, GC-B and C-receptor in the lung. Permanent removal of ANP in homozygous mutant ANP-/- mice resulted in significantly higher mRNA levels of GC-A and GC-B, and significantly lower C-receptor mRNA levels compared to wild type mice.
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