Department of Aquatic Biosciences, National Chiayi University, 300 University Road, Chiayi, 600, Taiwan, Republic of China.
Institute of Cellular and Organismic Biology, Academia Sinica, Nankang, Taipei, Taiwan, Republic of China.
Fish Physiol Biochem. 2012 Aug;38(4):977-988. doi: 10.1007/s10695-011-9583-z. Epub 2011 Dec 17.
The mRNA expression levels of Ca²⁺ transporter genes including the epithelial calcium channel (ECaC), sodium/calcium exchanger 1b (NCX1b), and plasma membrane calcium ATPase 2 (PMCA2) were measured in zebrafish larvae after exposure to 0.08 μM Cd²⁺ in either water mixed with 0.2 mM Ca²⁺ (lCa) or 2 mM Ca²⁺ (hCa). The ECaC and NCX1b expression decreased at the 48 and 72 h mark, respectively; however, PMCA2 transcripts decreased at 96 h after exposure to Cd²⁺ in lCa environment. On the other hand, the ECaC transcripts were not affected; however, the PMCA2 transcripts were increased at 72 h, while the NCX1b transcripts significantly decreased at 48 and 96 h after exposure to Cd²⁺ in a hCa environment. The Ca²⁺ contents of larvae significantly decreased after Cd²⁺ exposure in a lCa environment; however, the Ca²⁺ contents were evidently higher after exposure to Cd²⁺ in a hCa environment, except for 48th h mark. In addition, ECaC morphants showed lower Ca²⁺ contents of whole-body, and there were higher levels of mortality after exposure to the same condition compared to the wild-type groups. In contrast, injection of ECaC cRNA resulted in an increase in Ca²⁺ content and the rate of Ca²⁺ influx in zebrafish embryos. Summary, the results showed that the Ca²⁺ transporters of zebrafish larvae were impacted after exposures of 0.08 μM Cd. However, in the exposure condition, the ECaC and PMCA2 transcripts could be restored to control levels after the fish were treated in an environment with hCa.
在暴露于 0.08 μM Cd ²⁺ 的条件下,测量了斑马鱼幼虫中包括上皮钙通道(ECaC)、钠/钙交换蛋白 1b(NCX1b)和质膜钙 ATP 酶 2(PMCA2)在内的 Ca²⁺ 转运基因的 mRNA 表达水平。在含有 0.2 mM Ca²⁺(lCa)或 2 mM Ca²⁺(hCa)的水中暴露后,48 和 72 h 时 ECaC 和 NCX1b 表达分别下降;然而,暴露于 lCa 环境中的 Cd ²⁺ 96 h 后 PMCA2 转录物减少。另一方面,ECaC 转录物不受影响;然而,暴露于 hCa 环境中的 Cd ²⁺ 72 h 时 PMCA2 转录物增加,而 48 和 96 h 时 NCX1b 转录物显著减少。在 lCa 环境中暴露于 Cd ²⁺ 后,幼虫的 Ca²⁺ 含量显著降低;然而,暴露于 hCa 环境中的 Cd ²⁺ 后,Ca²⁺ 含量明显升高,除了 48 h 标记外。此外,ECaC 形态发生缺陷型表现出较低的全身 Ca²⁺ 含量,并且在暴露于相同条件下的死亡率高于野生型。相比之下,注射 ECaC cRNA 导致斑马鱼胚胎的 Ca²⁺ 含量增加和 Ca²⁺ 内流率增加。总之,结果表明 0.08 μM Cd 暴露后,斑马鱼幼虫的 Ca²⁺ 转运体受到影响。然而,在暴露条件下,当鱼在 hCa 环境中处理后,ECaC 和 PMCA2 转录物可以恢复到对照水平。