Role of Vitamin D on the Inhibition of Gastrin Production After Cisplatin Treatment

In rats cisplatin induces hypocalcemia, bloating of the stomach, and ulceration ameliorated through calcium supplements. This study was undertaken to test the role of calcium on the gastrin mRNA production in vitro and in vivo. RIN B6 cells were cultured in medium with calcium (1.8, 3.6 and 7.2 mM) and the active form of vitamin D (calcijex). Cisplatin was added (10 μg/ml) for 12 hrs and cells were harvested for RNA from various treatment groups. Male Wistar rats were treated with cisplatin (9 mg/kg), before and after vitamin D (0.3 mg/100g/week). The rats were killed and stomach tissues excised on 1, 6, 10 and 15 days after cisplatin treatment. RNA from the stomach was analyzed using the northern blot technique. Gastrin mRNA was suppressed after cisplatin treatment both in vitro and in vivo. In vitro calcium but not vitamin D additions partially prevented the gastrin mRNA. In vivo, however, vitamin D and calcium were equally effective in preventing gastrin mRNA loss

Negative feedback regulation of Wnt signaling by G beta gamma-mediated reduction of Dishevelled

Writ signaling is known to be important for diverse embryonic and post-natal cellular events and be regulated by the proteins Dishevelled and Axin. Although Dishevelled is activated by Writ and involved in signal transduction, it is not clear how Dishevelled-mediated signaling is turned off. We report that guanine nucleotide binding protein beta 2 (Gnb2; G beta(2)) bound to Axin and G beta(2) inhibited Writ mediated reporter activity. The inhibition involved reduction of the level of Dishevelled, and the G beta(2)gamma(2) mediated reduction of Dishevelled was countered by increased expression of Axin. Consistent with these effects in HEK293T cells, injection of G beta(2)gamma(2) into Xenopus embryos inhibited the formation of secondary axes induced either by XWnt8 or Dishevelled, but not by beta-catenin. The DEP domain of Dishevelled is necessary for both interaction with G beta(2)gamma(2) and subsequent degradation of Dishevelled via the lysosomal pathway. Signaling induced by G beta(2)gamma(2) is required because a mutant of G beta(2), G beta(2) (W332A) with lower signaling activity, had reduced ability to downregulate the level of Dishevelled. Activation of Writ signaling by either of two methods, increased Frizzled signaling or transient transfection of Writ, also led to increased degradation of Dishevelled and the induced Dishevelled loss is dependent on G beta(1) and G beta(2). Other studies with agents that interfere with PLC action and calcium signaling suggested that loss of Dishevelled is mediated through the following pathway: Wnt/Frizzled -> G beta gamma -> PLC - Ca+2/PKC signaling. Together the evidence suggests a novel negative feedback mechanism in which G beta(2)gamma(2) inhibits Writ signaling by degradation of Dishevelled.open111922sciescopuskc