Hagedorn Monica, Ziegler Andreas
Zentrale Einrichtung Elektronenmikroskopie, Universität Ulm, 89069 Ulm, Germany.
J Exp Biol. 2002 Jul;205(Pt 13):1935-42. doi: 10.1242/jeb.205.13.1935.
In terrestrial isopods, large amounts of Ca(2+) are transported across anterior sternal epithelial cells during moult-related deposition and resorption of CaCO(3) deposits. Because of its toxicity and function as a second messenger, resting cytosolic Ca(2+) levels must be maintained below critical concentrations during epithelial Ca(2+) transport, raising the possibility that organelles play a role during Ca(2+) transit. We therefore studied the uptake of Ca(2+) into Ca(2+)-sequestering organelles by monitoring the formation of birefringent calcium oxalate crystals in permeabilised anterior and posterior sternal epithelium cells of Porcellio scaber during Ca(2+)-transporting and non-transporting stages of the moulting cycle using polarised-light microscopy. The results indicate ATP-dependent uptake of Ca(2+) into organelles. Half-maximal crystal growth at a Ca(2+) activity, a(Ca), of 0.4 micromol l(-1) and blockade by cyclopiazonic acid suggest Ca(2+) uptake into the smooth endoplasmic reticulum by the smooth endoplasmic reticulum Ca(2+)-ATPase. Analytical electron microscopical techniques support this interpretation by revealing the accumulation of Ca(2+)-containing crystals in smooth membranous intracellular compartments. A comparison of different moulting stages demonstrated a virtual lack of crystal formation in the early premoult stage and a significant fivefold increase between mid premoult and the Ca(2+)-transporting stages of late premoult and intramoult. These results suggest a contribution of the smooth endoplasmic reticulum as a transient Ca(2+) store during intracellular Ca(2+) transit.
在陆生等足类动物中,大量的Ca(2+)在与蜕皮相关的碳酸钙沉积和再吸收过程中跨前胸腺上皮细胞运输。由于其毒性以及作为第二信使的功能,在前胸腺上皮细胞Ca(2+)运输过程中,静息细胞质Ca(2+)水平必须维持在临界浓度以下,这增加了细胞器在Ca(2+)转运过程中发挥作用的可能性。因此,我们通过使用偏光显微镜监测在蜕皮周期的Ca(2+)运输和非运输阶段,糙背石鳖前胸腺上皮细胞和后胸腺上皮细胞通透化后草酸钙双折射晶体的形成,来研究Ca(2+)进入Ca(2+)螯合细胞器的摄取情况。结果表明Ca(2+)以ATP依赖的方式摄取到细胞器中。在Ca(2+)活性a(Ca)为0.4 μmol l(-1)时晶体生长达到半最大值,且被环匹阿尼酸阻断,这表明Ca(2+)通过光滑内质网Ca(2+)-ATPase被摄取到光滑内质网中。分析电子显微镜技术通过揭示含Ca(2+)晶体在光滑膜性细胞内区室中的积累来支持这一解释。不同蜕皮阶段的比较表明,在蜕皮前期早期几乎没有晶体形成,而在蜕皮前期中期与蜕皮前期后期和蜕皮期的Ca(2+)运输阶段之间晶体形成显著增加了五倍。这些结果表明,光滑内质网作为细胞内Ca(2+)转运过程中的一个临时Ca(2+)储存库发挥了作用。