Zinc enhancement of LLC-PK1 renal epithelial barrier function

被引:10
|
作者
Wang, Xuexuan [1 ]
Valenzano, Mary Carmen [1 ]
Mercado, Joanna M. [1 ]
Zurbach, E. Peter [2 ]
Flounders, Christopher J. [3 ]
Mullin, James M. [1 ,4 ]
机构
[1] Lankenau Med Ctr, Wynnewood, PA 19096 USA
[2] St Josephs Univ, Dept Chem, Philadelphia, PA 19131 USA
[3] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
[4] Lankenau Med Ctr, Div Gastroenterol, Wynnewood, PA 19096 USA
关键词
LLC-PK1; Tight junction; Zinc; Claudin; CACO-2; Nutrition; PROTEIN-KINASE-C; TIGHT JUNCTION PERMEABILITY; TUMOR-NECROSIS-FACTOR; INTESTINAL PERMEABILITY; CELLULAR ZINC; CELLS; SUPPLEMENTATION; OVEREXPRESSION; DEFICIENCY; OCCLUDIN;
D O I
10.1016/j.clnu.2013.05.001
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background and aims: Earlier work by our group and others has documented improvement of epithelial barrier function in human gastrointestinal models. Here we tested zinc's ability to improve a renal epithelial model. Our aim was to compare the functional and structural effects of zinc on the tight junctional (TJ) complexes of these two very distinct epithelial cell types. Zinc's ability to achieve barrier enhancement in very different epithelial cell types by action upon distinct molecular targets in each epithelial model may suggest a fundamental general role for supplemental zinc in epithelial barrier improvement throughout the body. Methods: Cell layers were exposed to 50 or 100 mu M zinc on both cell surfaces for 48 h followed by measurement of transepithelial electrical resistance (R-t) and transepithelial C-14-mannitol flux J(m)). TJ proteins in cell layers were analyzed by Western immunoblot. Results and conclusions: Zinc supplementation improved the basal TJ barrier function of LLC-PK1 renal cell layers, exemplified by increased R-t and decreased J(m). These zinc-induced changes were also accompanied by decreased NaCl dilution potentials. Of the tight junctional proteins that were tested (occludin, claudins 1, 2, 3, 4, and 5, and tricellulin), we did not observe a zinc-induced change in abundance of any of them, in detergent-soluble fractions of lysates of confluent differentiated cell layers. However, examination of cytosolic fractions showed concentration-dependent increases in the levels of claudins -2 and -4 in this compartment as a result of supplemental zinc. The effects of supplemental zinc on the tight junctional complexes and barrier properties of this renal epithelial model are contrasted with zinc effects on the CACO-2 gastrointestinal model. (C) 2013 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.
引用
收藏
页码:280 / 286
页数:7
相关论文
共 50 条
  • [21] ORGANIZATION OF THE ENDOPLASMIC-RETICULUM IN RENAL-CELL LINES MDCK AND LLC-PK1
    BERGERON, M
    THIERY, G
    LENOIR, F
    GIOCONDI, MC
    LEGRIMELLEC, C
    CELL AND TISSUE RESEARCH, 1994, 277 (02) : 297 - 307
  • [22] Molecular Mechanisms Linking Empagliflozin to Renal Protection in the LLC-PK1 Model of Diabetic Nephropathy
    Mihaljevic, Vjera
    Zjalic, Milorad
    Kizivat, Tomislav
    Kolaric, Tea Omanovic
    Smolic, Martina
    Rodak, Edi
    Covic, Marina
    Kuna, Lucija
    Smolic, Robert
    Vcev, Aleksandar
    Curcic, Ines Bilic
    BIOMEDICINES, 2022, 10 (11)
  • [23] Solubilization of oxytocin receptors in porcine renal LLC-PK1 cell membranes
    FlanaganCato, LM
    Moga, CN
    Fluharty, SJ
    PEPTIDES, 1996, 17 (02) : 251 - 256
  • [24] CHARACTERIZATION OF THE SYNTHESIS AND RELEASE OF DOPAMINE IN LLC-PK1 CELLS
    DAWSON, R
    FELHEIM, R
    PHILLIPS, MI
    RENAL PHYSIOLOGY AND BIOCHEMISTRY, 1994, 17 (02): : 85 - 100
  • [25] Roles of oxygen radical production and lipid peroxidation in the cytotoxicity of cephaloridine on cultured renal epithelial cells (LLC-PK1)
    Kiyomiya, K
    Matsushita, N
    Matsuo, S
    Kurebe, M
    JOURNAL OF VETERINARY MEDICAL SCIENCE, 2000, 62 (09): : 977 - 981
  • [26] Kinetic analysis of tetraethylammonium transport in the kidney epithelial cell line, LLC-PK1
    Tomita, Y
    Otsuki, Y
    Hashimoto, Y
    Inui, K
    PHARMACEUTICAL RESEARCH, 1997, 14 (09) : 1236 - 1240
  • [27] Cisplatin-induced toxicity in LLC-PK1 kidney epithelial cells:: role of basolateral membrane transport
    Okuda, M
    Tsuda, K
    Masaki, K
    Hashimoto, Y
    Inui, K
    TOXICOLOGY LETTERS, 1999, 106 (2-3) : 229 - 235
  • [28] Effects of arbekacin and vancomycin on release of lactate dehydrogenase and fragmentation of DNA in LLC-PK1 kidney epithelial cells
    Nakamura, T
    Kokuryo, T
    Okuda, M
    Hashimoto, Y
    Inui, KI
    PHARMACEUTICAL RESEARCH, 1999, 16 (07) : 1132 - 1135
  • [29] NUCLEOSIDE TRANSPORT IN CULTURED LLC-PK1 EPITHELIA
    GRIFFITH, DA
    DOHERTY, AJ
    JARVIS, SM
    BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1106 (02) : 303 - 310
  • [30] Secretion mode and subcellular localization of human interferon-β exogenously expressed in porcine renal epithelial LLC-PK1 cells
    Nishio, T
    Maruyama, M
    Yoshida, T
    Watanabe, Y
    Nishikawa, M
    Takakura, Y
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2004, 27 (10) : 1653 - 1655