Delivery and Transcriptome Assessment of an In Vitro Three-Dimensional Proximal Tubule Model Established by Human Kidney 2 Cells in Clinical Gelatin Sponges

被引:0
|
作者
Hsiao, Hui-Yi [1 ,2 ]
Yen, Tzung-Hai [3 ,4 ]
Wu, Fang-Yu [5 ]
Cheng, Chao-Min [6 ]
Liu, Jia-Wei [2 ]
Fan, Yu-Ting [5 ]
Huang, Jung-Ju [7 ]
Nien, Chung-Yi [5 ]
机构
[1] Chang Gung Univ, Coll Med, Dept Biomed Sci, Taoyuan 33302, Taiwan
[2] Linkuo Chang Gung Mem Hosp, Ctr Tissue Engn, Linkuo Branch, Taoyuan 33305, Taiwan
[3] Linkuo Chang Gung Mem Hosp, Clin Poison Ctr, Dept Nephrol, Taoyuan 33305, Taiwan
[4] Chang Gung Univ, Coll Med, Dept Nephrol, Taoyuan 33302, Taiwan
[5] Natl Cent Univ, Dept Life Sci, Taoyuan 32001, Taiwan
[6] Natl Tsing Hua Univ, Inst Biomed Engn, Hsinchu, Taiwan
[7] Linkou Chang Gung Mem Hosp, Dept Plast & Reconstruct Surg, Div Reconstruct Microsurg, Taoyuan 33305, Taiwan
关键词
proximal tubule cells; two-dimensional culture; three-dimensional culture; HK-2; cells; gelatin spongy scaffold; comparative transcriptome analysis; nephrotoxicity; ORGANIC ANION; HK-2; CELLS; CULTURE SYSTEMS; RNA-SEQ; TRANSPORTERS; EXPRESSION; LINE; INJURY; DRUGS;
D O I
10.3390/ijms242115547
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The high prevalence of kidney diseases and the low identification rate of drug nephrotoxicity in preclinical studies reinforce the need for representative yet feasible renal models. Although in vitro cell-based models utilizing renal proximal tubules are widely used for kidney research, many proximal tubule cell (PTC) lines have been indicated to be less sensitive to nephrotoxins, mainly due to altered expression of transporters under a two-dimensional culture (2D) environment. Here, we selected HK-2 cells to establish a simplified three-dimensional (3D) model using gelatin sponges as scaffolds. In addition to cell viability and morphology, we conducted a comprehensive transcriptome comparison and correlation analysis of 2D and 3D cultured HK-2 cells to native human PTCs. Our 3D model displayed stable and long-term growth with a tubule-like morphology and demonstrated a more comparable gene expression profile to native human PTCs compared to the 2D model. Many missing or low expressions of major genes involved in PTC transport and metabolic processes were restored, which is crucial for successful nephrotoxicity prediction. Consequently, we established a cost-effective yet more representative model for in vivo PTC studies and presented a comprehensive transcriptome analysis for the systematic characterization of PTC lines.
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页数:20
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