The presence of xanthine dehydrogenase is crucial for the maturation of the rat kidneys

被引:1
作者
Dissanayake, Lashodya V. [1 ]
Kravtsova, Olha [1 ]
Lowe, Melissa [1 ]
Mccrorey, Marice K. [2 ]
Van Beusecum, Justin P. [2 ,3 ]
Palygin, Oleg [2 ,4 ]
Staruschenko, Alexander [1 ,5 ,6 ]
机构
[1] Univ S Florida, Morsani Coll Med, Dept Mol Pharmacol & Physiol, Tampa, FL 33602 USA
[2] Med Univ South Carolina, Dept Med, Div Nephrol, Charleston, SC 29425 USA
[3] Ralph H Johnson Vet Affairs Healthcare Syst, Charleston, SC 29403 USA
[4] Med Univ South Carolina, Dept Regenerat Med & Cell Biol, Charleston, SC 29425 USA
[5] Univ S Florida, Hypertens & Kidney Res Ctr, Tampa, FL 33602 USA
[6] James A Haley Vet Hosp, Tampa, FL 33612 USA
基金
美国国家卫生研究院;
关键词
GENE-EXPRESSION; POSTNATAL-DEVELOPMENT; CELL-PROLIFERATION; GROWTH-FACTOR; IV COLLAGEN; CYCLOOXYGENASE-2; MORPHOGENESIS; ACTIVATION; OXIDOREDUCTASE; PATHOGENESIS;
D O I
10.1042/CS20231144
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The development of the kidney involves essential cellular processes, such as cell proliferation and differentiation, which are led by interactions between multiple signaling pathways. Xanthine dehydrogenase (XDH) catalyzes the reaction producing uric acid in the purine catabolism, which plays a multifaceted role in cellular metabolism. Our previous study revealed that the genetic ablation of the Xdh gene in rats leads to smaller kidneys, kidney damage, decline of renal functions, and failure to thrive. Rats, unlike humans, continue their kidney development postnatally. Therefore, we explored whether XDH plays a critical role in kidney development using SS-/- rats during postnatal development phase. XDH expression was significantly increased from postnatal day 5 to 15 in wild-type but not homozygote rat kidneys. The transcriptomic profile of renal tissue revealed several dysregulated pathways due to the lack of Xdh expression with the remodeling in inflammasome, purinergic signaling, and redox homeostasis. Further analysis suggested that lack of Xdh affects kidney development, likely via dysregulation of epidermal growth factor and its downstream STAT3 signaling. The present study showed that Xdh is essential for kidney maturation. Our data, alongside the previous research, suggests that loss of Xdh function leads to developmental issues, rendering them vulnerable to kidney diseases in adulthood.
引用
收藏
页码:269 / 288
页数:20
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