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The Post-Translational Modification Networking in WNK-Centric Hypertension Regulation and Electrolyte Homeostasis.


ABSTRACT: The with-no-lysine (WNK) kinase family, comprising four serine-threonine protein kinases (WNK1-4), were first linked to hypertension due to their mutations in association with pseudohypoaldosteronism type II (PHAII). WNK kinases regulate crucial blood pressure regulators, SPAK/OSR1, to mediate the post-translational modifications (PTMs) of their downstream ion channel substrates, such as sodium chloride co-transporter (NCC), epithelial sodium chloride (ENaC), renal outer medullary potassium channel (ROMK), and Na/K/2Cl co-transporters (NKCCs). In this review, we summarize the molecular pathways dysregulating the WNKs and their downstream target renal ion transporters. We summarize each of the genetic variants of WNK kinases and the small molecule inhibitors that have been discovered to regulate blood pressure via WNK-triggered PTM cascades.

SUBMITTER: Lin SC 

PROVIDER: S-EPMC9496095 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

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The Post-Translational Modification Networking in WNK-Centric Hypertension Regulation and Electrolyte Homeostasis.

Lin Shiuan-Chen SC   Ma Chun C   Chang Kao-Jung KJ   Cheong Han-Ping HP   Lee Ming-Cheng MC   Lan Yuan-Tzu YT   Wang Chien-Ying CY   Chiou Shih-Hwa SH   Huo Teh-Ia TI   Hsu Tsui-Kang TK   Tsai Ping-Hsing PH   Yang Yi-Ping YP  

Biomedicines 20220902 9


The with-no-lysine (WNK) kinase family, comprising four serine-threonine protein kinases (WNK1-4), were first linked to hypertension due to their mutations in association with pseudohypoaldosteronism type II (PHAII). WNK kinases regulate crucial blood pressure regulators, SPAK/OSR1, to mediate the post-translational modifications (PTMs) of their downstream ion channel substrates, such as sodium chloride co-transporter (NCC), epithelial sodium chloride (ENaC), renal outer medullary potassium chan  ...[more]

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