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胱硫醚γ-裂解酶在急性缺血性肾损伤所致即刻肾损伤及炎症反应中的作用

Role of Cystathionine Gamma-Lyase in Immediate Renal Impairment and Inflammatory Response in Acute Ischemic Kidney Injury.

作者信息

Markó Lajos, Szijártó István A, Filipovic Milos R, Kaßmann Mario, Balogh András, Park Joon-Keun, Przybyl Lukasz, N'diaye Gabriele, Krämer Stephanie, Anders Juliane, Ishii Isao, Müller Dominik N, Gollasch Maik

机构信息

Experimental and Clinical Research Center, a joint cooperation between the Charité Medical Faculty and the Max-Delbrück Center (MDC) for Molecular Medicine, Berlin, Germany.

Max-Delbrück Center (MDC) for Molecular Medicine, Berlin, Germany.

出版信息

Sci Rep. 2016 Jun 8;6:27517. doi: 10.1038/srep27517.

Abstract

Hydrogen sulfide (H2S) is known to act protectively during renal ischemia/reperfusion injury (IRI). However, the role of the endogenous H2S in acute kidney injury (AKI) is largely unclear. Here, we analyzed the role of cystathionine gamma-lyase (CTH) in acute renal IRI using CTH-deficient (Cth(-/-)) mice whose renal H2S levels were approximately 50% of control (wild-type) mice. Although levels of serum creatinine and renal expression of AKI marker proteins were equivalent between Cth(-/-) and control mice, histological analysis revealed that IRI caused less renal tubular damage in Cth(-/-) mice. Flow cytometric analysis revealed that renal population of infiltrated granulocytes/macrophages was equivalent in these mice. However, renal expression levels of certain inflammatory cytokines/adhesion molecules believed to play a role in IRI were found to be lower after IRI only in Cth(-/-) mice. Our results indicate that the systemic CTH loss does not deteriorate but rather ameliorates the immediate AKI outcome probably due to reduced inflammatory responses in the kidney. The renal expression of CTH and other H2S-producing enzymes was markedly suppressed after IRI, which could be an integrated adaptive response for renal cell protection.

摘要

已知硫化氢(H₂S)在肾脏缺血/再灌注损伤(IRI)过程中发挥保护作用。然而,内源性H₂S在急性肾损伤(AKI)中的作用在很大程度上尚不清楚。在此,我们使用胱硫醚γ-裂解酶(CTH)缺陷(Cth⁻/⁻)小鼠分析了CTH在急性肾IRI中的作用,这些小鼠的肾脏H₂S水平约为对照(野生型)小鼠的50%。尽管Cth⁻/⁻小鼠与对照小鼠之间的血清肌酐水平和AKI标志物蛋白的肾脏表达相当,但组织学分析显示,IRI在Cth⁻/⁻小鼠中引起的肾小管损伤较轻。流式细胞术分析显示,这些小鼠中浸润的粒细胞/巨噬细胞的肾脏数量相当。然而,仅在IRI后的Cth⁻/⁻小鼠中发现,某些被认为在IRI中起作用的炎性细胞因子/黏附分子的肾脏表达水平较低。我们的结果表明,全身性CTH缺失不会使急性AKI结果恶化,反而可能由于肾脏炎症反应减轻而改善急性AKI结果。IRI后,CTH和其他产H₂S酶的肾脏表达明显受到抑制,这可能是一种用于肾细胞保护的综合适应性反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b31/4897642/8172c5eca47b/srep27517-f1.jpg

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