Key result
Calcium removal or aprotinin blocks stretch-induced atriopeptin prohormone cleavage in rat hearts, implicating extracellular processing.
Why the study?
The mechanisms and site of prohormone processing of atriopeptin after atrial stretch in the perfused rat heart were not fully understood.
The study demonstrates that the proteolytic processing of atriopeptin prohormone to its mature form occurs in the extracellular space and requires calcium, suggesting a concerted action between atrial myocytes and adjacent cells.
Answers are grounded in this paper and cite their sources.
Implicates extracellular calcium-dependent atriopeptin processing in rat hearts; leaves open relevance to human ANP regulation or therapy.
Atriopeptin (AP) is stored as the prohormone AP-126 [atrial natriuretic factor-(1-26)] in atrial granules. Cultured atrial myocytes synthesize and release only prohormone into the medium. HPLC analysis of the coronary venous effluent of media from perfused rat hearts subjected to right atrial stretch indicated the presence of the C-terminal mature hormone AP-28 [atrial natriuretic factor-(99-126)] and little or no prohormone. Absence of calcium from the perfusion medium increased total AP release and surprisingly blocked the proteolytic cleavage of the prohormone. Similarly, addition of the proteolytic inhibitor aprotinin to the perfusion medium suppressed the processing of the endogenous AP-126 released by atrial stretch. Aprotinin would be restricted to the extracellular space, which is therefore implicated as the site of prohormone processing. This suggestion was validated by the demonstration that the perfused rat heart could readily cleave exogenous prohormone to mature hormone, a process blocked by aprotinin. Hypothetically, the stimulus-release-processing event initiated by atrial stretch may require the concerted action of the synthetic cell (i.e., atrial myocyte) and a processing cell or site (e.g., the adjacent atrial mesenchymal cell) for the production of the mature AP-28, which is the circulating molecular form of this endocrine system.
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Ito et al. (1988) studied this question. Absence of calcium or addition of aprotinin was evaluated on Atriopeptin prohormone release and processing. In perfused rat hearts, absence of calcium or addition of aprotinin blocked the proteolytic cleavage of atriopeptin prohormone released by atrial stretch, implicating the extracellular space in processing.
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