Walski Tomasz, De Schutter Kristof, Cappelle Kaat, Van Damme Els J M, Smagghe Guy
Department of Crop Protection, Ghent University, Ghent, Belgium.
Department of Molecular Biotechnology, Ghent University, Ghent, Belgium.
Front Physiol. 2017 Dec 8;8:1020. doi: 10.3389/fphys.2017.01020. eCollection 2017.
Glycans are involved in many biological phenomena, including signal transduction, cell adhesion, immune response or differentiation. Although a few papers have reported on the role of glycans in the development and proper functioning of the insect midgut, no data are available regarding the localization of the glycan structures on the surface of the cells in the gut of insects. In this paper, we analyzed the spatial distribution of glycans present on the surface of the midgut cells in larvae of the cotton leafworm , an important agricultural pest insect worldwide. For this purpose, we established primary midgut cell cultures, probed these individual cells that are freely suspended in liquid medium with a selection of seven fluorescently labeled lectins covering a range of different carbohydrate binding specificities [mannose oligomers (GNA and HHA), GalNAc/Gal (RSA and SSA), GlcNAc (WGA and Nictaba) and Neu5Ac(α-2,6)Gal/GalNAc (SNA-I)], and visualized the interaction of these lectins with the different zones of the midgut cells using confocal microscopy. Our analysis focused on the typical differentiated columnar cells with a microvillar brush border at their apical side, which are dominantly present in the Lepidopteran midgut and function in food digestion and absorption, and as well as on the undifferentiated stem cells that are important for midgut development and repair. Confocal microscopy analyses showed that the GalNAc/Gal-binding lectins SSA and RSA and the terminal GlcNAc-recognizing WGA bound preferentially to the apical microvillar zone of the differentiated columnar cells as compared to the basolateral pole. The reverse result was observed for the mannose-binding lectins GNA and HHA, as well as Nictaba that binds preferentially to GlcNAc oligomers. Furthermore, differences in lectin binding to the basal and lateral zones of the cell membranes of the columnar cells were apparent. In the midgut stem cells, GNA and Nictaba bound more strongly to the membrane of these undifferentiated cells compared to the microvillar pole of the columnar cells, while SSA, HHA, WGA, and SNA-I showed stronger binding to the microvilli. Our results indicated that polarization of the midgut cells is also reflected by a specific distribution of glycans, especially between the basal and microvillar pole. The data are discussed in relation to the functioning and development of the insect midgut.
聚糖参与许多生物学现象,包括信号转导、细胞黏附、免疫反应或分化。尽管有几篇论文报道了聚糖在昆虫中肠发育和正常功能中的作用,但关于昆虫肠道细胞表面聚糖结构的定位尚无相关数据。在本文中,我们分析了棉铃虫(一种全球重要的农业害虫)幼虫中肠细胞表面存在的聚糖的空间分布。为此,我们建立了原代中肠细胞培养物,用七种荧光标记的凝集素对这些自由悬浮在液体培养基中的单个细胞进行检测,这些凝集素涵盖了一系列不同的碳水化合物结合特异性[甘露糖寡聚物(GNA和HHA)、GalNAc/Gal(RSA和SSA)、GlcNAc(WGA和Nictaba)以及Neu5Ac(α-2,6)Gal/GalNAc(SNA-I)],并使用共聚焦显微镜观察这些凝集素与中肠细胞不同区域的相互作用。我们的分析集中在典型的分化柱状细胞,其顶端侧有微绒毛刷状缘,在鳞翅目昆虫中肠中占主导地位,具有食物消化和吸收功能,以及对中肠发育和修复很重要的未分化干细胞。共聚焦显微镜分析表明,与基底外侧极相比,GalNAc/Gal结合凝集素SSA和RSA以及识别末端GlcNAc的WGA优先结合到分化柱状细胞的顶端微绒毛区。对于甘露糖结合凝集素GNA和HHA以及优先结合GlcNAc寡聚物的Nictaba,观察到相反的结果。此外,凝集素与柱状细胞膜的基底和外侧区域结合的差异很明显。在中肠干细胞中,与柱状细胞的微绒毛极相比,GNA和Nictaba与这些未分化细胞的膜结合更强,而SSA、HHA、WGA和SNA-I与微绒毛的结合更强。我们的结果表明,中肠细胞的极化也通过聚糖的特定分布反映出来,尤其是在基底和微绒毛极之间。本文结合昆虫中肠的功能和发育对这些数据进行了讨论。