Padmakumar Vc, Masiuk Katelyn E, Luger Dror, Lee Christina, Coppola Vincenzo, Tessarollo Lino, Hoover Shelley B, Karavanova Irina, Buonanno Andres, Simpson R Mark, Yuspa Stuart H
Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD, USA.
BMC Dev Biol. 2014 May 28;14:24. doi: 10.1186/1471-213X-14-24.
Chloride Intracellular Channel 4 (CLIC4) is one of seven members in the closely related CLIC protein family. CLIC4 is involved in multiple cellular processes including apoptosis, cellular differentiation, inflammation and endothelial tubulogenesis. Despite over a decade of research, no comprehensive in situ expression analysis of CLIC4 in a living organism has been reported. In order to fulfill this goal, we generated a knock-in mouse to express Green Fluorescent Protein (GFP) from the CLIC4 locus, thus substituting the GFP coding region for CLIC4. We used GFP protein expression to eliminate cross reaction with other CLIC family members.
We analyzed CLIC4 expression during embryonic development and adult organs. During mid and late gestation, CLIC4 expression is modulated particularly in fetal brain, heart, thymus, liver and kidney as well as in developing brown adipose tissue and stratifying epidermis. In the adult mouse, CLIC4 is highly expressed globally in vascular endothelial cells as well as in liver, lung alveolar septae, pancreatic acini, spermatogonia, renal proximal tubules, cardiomyocytes and thymic epithelial cells. Neural expression included axonal tracks, olfactory bulb, Purkinje cell layer and dentate gyrus. Renal CLIC4 expression was most pronounced in proximal tubules, although altered renal function was not detected in the absence of CLIC4. Myeloid cells and B cells of the spleen are rich in CLIC4 expression as are CD4 and CD8 positive T cells.
In a comprehensive study detailing CLIC4 expression in situ in a mouse model that excludes cross reaction with other family members, we were able to document previously unreported expression for CLIC4 in developing fetus, particularly the brain. In addition, compartmentalized expression of CLIC4 in specific adult tissues and cells provides a focus to explore potential functions of this protein not addressed previously.
氯离子细胞内通道蛋白4(CLIC4)是密切相关的CLIC蛋白家族的七个成员之一。CLIC4参与多种细胞过程,包括细胞凋亡、细胞分化、炎症和内皮细胞管生成。尽管经过了十多年的研究,但尚未有关于CLIC4在活体生物中的全面原位表达分析的报道。为了实现这一目标,我们构建了一种敲入小鼠,使其从CLIC4基因座表达绿色荧光蛋白(GFP),从而用GFP编码区替代CLIC4。我们利用GFP蛋白表达消除与其他CLIC家族成员的交叉反应。
我们分析了胚胎发育和成年器官中CLIC4的表达情况。在妊娠中期和晚期,CLIC4的表达受到调控,尤其在胎儿脑、心脏、胸腺、肝脏和肾脏以及发育中的棕色脂肪组织和分层表皮中。在成年小鼠中,CLIC4在血管内皮细胞以及肝脏、肺泡隔、胰腺腺泡、精原细胞、肾近端小管、心肌细胞和胸腺上皮细胞中广泛高表达。神经表达包括轴突束、嗅球、浦肯野细胞层和齿状回。肾CLIC4表达在近端小管中最为明显,尽管在缺乏CLIC4的情况下未检测到肾功能改变。脾脏的髓样细胞和B细胞富含CLIC4表达,CD4和CD8阳性T细胞也是如此。
在一项详细研究CLIC4在小鼠模型中的原位表达且排除与其他家族成员交叉反应的综合性研究中,我们得以记录CLIC4在发育中的胎儿,尤其是大脑中以前未报道的表达情况。此外,CLIC4在特定成年组织和细胞中的分区表达为探索该蛋白以前未涉及到的潜在功能提供了重点研究方向。