Epithelial Signaling and Transport Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institute of Health, Bethesda, Maryland, USA.
Physiology (Bethesda). 2012 Oct;27(5):291-9. doi: 10.1152/physiol.00028.2012.
Fluid and electrolyte homeostasis is a fundamental physiological function required for survival and is associated with a plethora of diseases when aberrant. Systemic fluid and electrolyte composition is regulated by the kidney, and all secretory epithelia generate biological fluids with defined electrolyte composition by vectorial transport of ions and the obligatory water. A major regulatory pathway that immerged in the last several years is regulation of ion transporters by the WNK/SPAK kinases and IRBIT/PP1 pathways. The IRBIT/PP1 pathway functions to reverse the effects of the WNK/SPAK kinases pathway, as was demonstrated for NBCe1-B and CFTR. Since many transporters involved in fluid and electrolyte homeostasis are affected by PP1 and/or calcineurin, it is possible that WNK/SPAK and IRBIT/PP1 form a common regulatory pathway to tune the activity of fluid and electrolyte transport in response to physiological demands.
体液和电解质平衡是生存所必需的基本生理功能,当出现异常时,与许多疾病都有关联。肾脏调节全身的体液和电解质组成,所有分泌上皮细胞通过离子的向量运输和必需的水来产生具有特定电解质组成的生物液体。最近几年出现的一个主要调控途径是 WNK/SPAK 激酶和 IRBIT/PP1 途径对离子转运体的调控。IRBIT/PP1 途径的作用是逆转 WNK/SPAK 激酶途径的作用,这在 NBCe1-B 和 CFTR 中得到了证明。由于许多参与体液和电解质平衡的转运体受到 PP1 和/或钙调神经磷酸酶的影响,WNK/SPAK 和 IRBIT/PP1 有可能形成一个共同的调节途径,以根据生理需求调节流体和电解质转运的活性。