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Kidney injury: the spleno-renal connection and splenic tyrosine kinase.

作者信息

Almasry Yazan, Alodhaibi Ibrahim, Nammor Talah, Lerman Amir, Lerman Lilach O, Zhu Xiang-Yang

机构信息

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, 55901, USA.

College of Medicine, Alfaisal University, 11543, Riyadh, Saudi Arabia.

出版信息

J Nephrol. 2024 Nov;37(8):2151-2160. doi: 10.1007/s40620-024-02121-4. Epub 2024 Oct 10.


DOI:10.1007/s40620-024-02121-4
PMID:39388044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11872174/
Abstract

Kidney injury is a major medical burden and one of the most common reasons for hospitalization and poor life quality. Kidney injury can include acute kidney injury, chronic kidney disease, and immune-mediated kidney diseases most of which have no definitive therapy. The spleen is a secondary lymphoid organ in the reticuloendothelial system that plays an important role in protecting the body from various diseases. Notably, spleen tyrosine kinase, a non-receptor tyrosine kinase, is a crucial player that aids in immunity and protection and is highly expressed in the kidney and hematopoietic cells. It has been shown that alterations in spleen tyrosine kinase function or expression could lead to a wide range of diseases and abnormalities. Over the past decade, the role of spleen and spleen tyrosine kinase in multiple kidney diseases has emerged. Evidence suggests that modulating the spleno-renal connection through activation of the cholinergic anti-inflammatory pathway can be a promising strategy for protecting against kidney injury. Imitating the protective function of the spleen through interleukin-10-extracellular vesicles can also be of therapeutic value. In addition, evidence showed that inhibition of the spleen tyrosine kinase leads to amelioration of the kidney injury. However, further exploration and long-term studies are needed to unravel the spleno-renal connection, as well as the efficacy of spleen tyrosine kinase inhibitors, before they can be used as means for treatment of kidney injury.

摘要

相似文献

[1]
Kidney injury: the spleno-renal connection and splenic tyrosine kinase.

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[2]
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[3]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Recent advances in understanding spleen tyrosine kinase (SYK) in human biology and disease, with a focus on fostamatinib.

Platelets. 2023-12

[2]
The α7 nicotinic acetylcholine receptor agonist PNU-282987 ameliorates sepsis-induced acute kidney injury through CD4+CD25+ regulatory T cells in rats.

Bosn J Basic Med Sci. 2022-10-23

[3]
History of proliferative glomerulonephritis predicts end stage kidney disease in pure membranous lupus nephritis.

Rheumatology (Oxford). 2022-5-30

[4]
Acute kidney injury.

Nat Rev Dis Primers. 2021-7-15

[5]
Vagus nerve stimulation activates two distinct neuroimmune circuits converging in the spleen to protect mice from kidney injury.

Proc Natl Acad Sci U S A. 2021-3-23

[6]
Chronic kidney disease: Definition, updated epidemiology, staging, and mechanisms of increased cardiovascular risk.

J Clin Hypertens (Greenwich). 2021-4

[7]
Phase II, randomised, double-blind, multicentre study evaluating the safety and efficacy of filgotinib and lanraplenib in patients with lupus membranous nephropathy.

RMD Open. 2020-12

[8]
Mechanisms of Renal-Splenic Axis Involvement in Acute Kidney Injury Mediated by the α7nAChR-NF-κB Signaling Pathway.

Inflammation. 2021-4

[9]
Extracellular vesicle-encapsulated IL-10 as novel nanotherapeutics against ischemic AKI.

Sci Adv. 2020-8-12

[10]
Role of spleen-derived CD11b+Gr-1+ cells in sepsis-induced acute kidney injury.

Clin Invest Med. 2020-6-28

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