Why the study?
The dysregulation of K+ channels is a hallmark of pulmonary arterial hypertension, prompting an analysis of the cationic channelome in patient lungs.
Transcriptomic analysis reveals that widespread downregulation of cationic channels is a signature of advanced pulmonary arterial hypertension across different etiologies.
Supports cationic channel dysregulation as a PAH signature; hypothesis-generating and requires validation before clinical or therapeutic translation.
The dysregulation of K + channels is a hallmark of pulmonary arterial hypertension (PAH). Herein, the channelome was analyzed in lungs of patients with PAH in a public transcriptomic database. Sixty six (46%) mRNA encoding cationic channels were dysregulated in PAH with most of them downregulated (83%). The principal component analysis indicated that dysregulated cationic channel expression is a signature of the disease. Changes were very similar in idiopathic, connective tissue disease and congenital heart disease associated PAH. This analysis 1) is in agreement with the widely recognized pathophysiological role of TASK1 and K V 1.5, 2) supports previous preliminary reports pointing to the dysregulation of several K + channels including the downregulation of K V 1.1, K V 1.4, K V 1.6, K V 7.1, K V 7.4, K V 9.3 and TWIK2 and the upregulation of K Ca 1.1 and 3) points to other cationic channels dysregulated such as Kv7.3, TALK2, Ca V 1 and TRPV4 which might play a pathophysiological role in PAH. The significance of other changes found in Na + and TRP channels remains to be investigated.
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Pérez‐Vizcaíno et al. (2021) studied this question.
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