Inhibition of cell differentiation by G alpha q in the renal epithelial cell line LLC-PK1.
Inhibition of cell differentiation by G alpha q in the renal epithelial cell line LLC-PK1.
复制标题
G α q 对肾上皮细胞系 LLC-PK1 中细胞分化的抑制。
DOI：
10.1152/ajpcell.1998.274.4.c1030
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发表时间：
1998
期刊：
影响因子：
--
通讯作者：
Weiss,ER
中科院分区：
文献类型：
--
作者：
Sun,L;Weaver,DJ;Amsler,K;Weiss,ER
LLC-PK1, an epithelial cell line derived from the kidney proximal tubule, was used to study the ability of the G protein α-subunit, Gαq, to regulate cell differentiation. A constitutively active mutant protein, αqQ209L, was expressed using the LacSwitch-inducible mammalian expression system. Induction of αqQ209L expression with isopropyl-β-d-thiogalactopyranoside (IPTG) enhanced phospholipase C activity maximally by 6- to 7.5-fold. Increasing concentrations of IPTG progressively inhibited the activity of two differentiation markers, Na+-dependent hexose transport and alkaline phosphatase activity. Induction of αqQ209L expression also caused a change from an epithelial to a spindle-shaped morphology. The effects of αqQ209L expression on cell differentiation were similar to those observed with 12-O-tetradecanoylphorbol 13-acetate (TPA) treatment. However, protein kinase C (PKC) levels were downregulated in TPA-treated cells but not in αqQ209L-expressing cells, suggesting that the regulation of PKC by Gαqmay be different from regulation by TPA. Interestingly, the PKC inhibitor GF-109203X did not inhibit the effect of IPTG on the development of Na+-dependent hexose transport in αqQ209L-expressing cells. These data implicate PKCδ and PKCε in the pathway used by Gαqto block the development of Na+-dependent hexose transport in IPTG-treated cells.
