Haque Md Ehsanul, Shrestha Swojani, Sens Donald A, Garrett Scott H
Department of Pathology, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58202, USA.
Cells. 2025 Jun 10;14(12):877. doi: 10.3390/cells14120877.
Arsenic, in the form of inorganic arsenite, is toxic to the kidney and can cause acute kidney injury, manifesting as destruction of proximal tubule cells. Nephron repair is possible through the proliferation of resident tubular progenitor cells expressing CD133 and CD24 surface markers. We simulated regenerative repair in the continued presence of i-As (III) using a cell culture model of a renal progenitor cell line expressing CD133 () and CD24. Continued exposure and subculturing of progenitor cells to i-As (III) led to a reduction in the expression of and CD24, as well as a decrease in the ability to differentiate into tubule-like structures. Cessation of i-As (III) and recovery for up to three passages resulted in continued repression of and reduced ability to differentiate. Chronically exposed cells exhibited an ability to form colonies in soft agar, suggesting neoplastic transformation. Chronically exposed cells also exhibited an induction of CD44, a cell surface marker commonly found in renal cell carcinoma, as well as in tubular repair in chronic renal injury such as chronic kidney disease. These results demonstrate potential adverse outcomes of renal progenitor cells chronically exposed to a nephrotoxicant, as well as in environmental exposure to arsenic.
无机亚砷酸盐形式的砷对肾脏有毒性,可导致急性肾损伤,表现为近端肾小管细胞的破坏。通过表达CD133和CD24表面标志物的驻留肾小管祖细胞的增殖,肾单位修复是可能的。我们使用表达CD133()和CD24的肾祖细胞系的细胞培养模型,在持续存在i-As(III)的情况下模拟再生修复。祖细胞持续暴露于i-As(III)并传代培养导致和CD24表达降低,以及分化为管状结构的能力下降。停止i-As(III)并恢复传代多达三代导致持续抑制并降低分化能力。长期暴露的细胞表现出在软琼脂中形成集落的能力,提示肿瘤转化。长期暴露的细胞还表现出CD44的诱导,CD44是肾细胞癌以及慢性肾损伤(如慢性肾病)肾小管修复中常见的细胞表面标志物。这些结果证明了肾祖细胞长期暴露于肾毒物以及环境中砷暴露的潜在不良后果。