Endothelin-1 production during the acute chest syndrome in sickle cell disease

SI Hammerman, S Kourembanas, TJ Conca… - American journal of …, 1997 - atsjournals.org
SI Hammerman, S Kourembanas, TJ Conca, M Tucci, M Brauer, HW Farber
American journal of respiratory and critical care medicine, 1997atsjournals.org
To investigate the role of the endothelial-derived vasoactive mediator endothelin (ET-1) in
the acute chest syndrome (ACS), we incubated bovine pulmonary artery endothelial cells
(BPAEC) with red blood cells (equivalent to a hematocrit of 20%) and/or autologous plasma
(1: 10 dilution) from two patients during ACS and during routine clinic visits. Cellular RNA
was analyzed for ET-1 transcripts by Northern analysis and ET-1 protein levels in BPAEC
supernatants and in plasma measured by radioimmunoassay. ET-1 mRNA expression and …
To investigate the role of the endothelial-derived vasoactive mediator endothelin (ET-1) in the acute chest syndrome (ACS), we incubated bovine pulmonary artery endothelial cells (BPAEC) with red blood cells (equivalent to a hematocrit of 20%) and/or autologous plasma (1:10 dilution) from two patients during ACS and during routine clinic visits. Cellular RNA was analyzed for ET-1 transcripts by Northern analysis and ET-1 protein levels in BPAEC supernatants and in plasma measured by radioimmunoassay. ET-1 mRNA expression and protein levels increased in BPAEC exposed to plasma obtained during ACS; in contrast, exposure to plasma obtained during routine clinic visits did not alter BPAEC ET-1 mRNA expression or protein levels. Plasma ET-1 level was elevated during ACS, decreased during resolution, and remained slightly elevated during routine clinic visits. Plasma obtained from one patient 4 d prior to hospitalization for vasoocclusive crisis contained the highest ET-1 level and markedly increased BPAEC ET-1 mRNA expression and protein levels. In both patients, BPAEC ET-1 mRNA and protein expression in vitro and plasma ET-1 levels in vivo correlated with stage of disease and occurred in the absence of direct erythrocyte contact in vitro. These observations suggest that ET-1 production contributes to development of ACS.
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