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内皮细胞释放出在体外支持丝虫长期存活的可溶性因子。

Endothelial cells release soluble factors that support the long-term survival of filarial worms in vitro.

作者信息

Evans Holly, Flynn Alexander Francis, Mitre Edward

机构信息

Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, United States.

Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, United States.

出版信息

Exp Parasitol. 2016 Nov;170:50-58. doi: 10.1016/j.exppara.2016.08.004. Epub 2016 Aug 24.

Abstract

The inability to maintain filarial nematodes in long-term in vitro culture greatly limits research into the basic biology of these parasites and hinders in vitro screening of novel anti-filarial agents. In this study, we sought to characterize nutrients that promote the long-term survival of filarial worms in vitro. Using microfilariae (MF) obtained from gerbils infected with Litomosoides sigmodontis, a filarial parasite of rodents, we found that Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS) resulted in MF survival of only 5 days. However, co-culturing MF with a mouse endothelial cell line (EOMA) enabled survival for 40 days. Culturing EOMA cells in transwell plates extended MF survival to the same degree as direct co-culture, suggesting that the factors microfilariae require are soluble in nature. Heat inactivation of EOMA conditioned media at 56 °C reduced MF survival by approximately 50%, and heat inactivation at 100 °C reduced survival to 3 days, demonstrating that both heat labile and heat stable factors are involved. EOMA cells require FBS to produce these factors, as conditioned media collected from EOMA cells grown in the absence of FBS failed to prolong survival. The removal of lipids also abrogated survival, indicating MF are likely utilizing lipid factors released by EOMA cells. Dialysis experiments demonstrate that at least some of the required factors are between 0.1 and 1 kDa in size. Importantly, L. sigmodontis adult worms also show significantly extended survival when cultured in EOMA conditioned media. Together, these results suggest that EOMA-produced factors include lipid-containing molecules, heat labile molecules (likely a protein), and micronutrients between 0.1 and 1 kDa in size. These studies have established a cell-free approach to maintaining MF and adult stage filarial worms in long-term in vitro culture and have taken important steps towards biochemically characterizing host-derived nutrients required for parasite survival.

摘要

无法在体外长期培养丝虫线虫极大地限制了对这些寄生虫基础生物学的研究,并阻碍了新型抗丝虫药物的体外筛选。在本研究中,我们试图确定能够促进丝虫在体外长期存活的营养物质。使用从感染了Sigmodontis丝虫(一种啮齿动物的丝虫寄生虫)的沙鼠体内获得的微丝蚴(MF),我们发现补充有10%胎牛血清(FBS)的杜氏改良 Eagle 培养基(DMEM)只能使 MF 存活5天。然而,将 MF 与小鼠内皮细胞系(EOMA)共培养可使其存活40天。在Transwell板中培养 EOMA 细胞可将 MF 存活期延长至与直接共培养相同的程度,这表明微丝蚴所需的因子本质上是可溶的。在56℃对 EOMA 条件培养基进行热灭活可使 MF 存活率降低约50%,而在100℃进行热灭活则使存活率降至3天,这表明热不稳定和热稳定因子都参与其中。EOMA 细胞需要 FBS 来产生这些因子,因为从无 FBS 条件下生长的 EOMA 细胞收集的条件培养基无法延长 MF 的存活期。去除脂质也会消除 MF 的存活,这表明 MF 可能利用 EOMA 细胞释放的脂质因子。透析实验表明,至少一些所需因子的大小在0.1至1 kDa之间。重要的是,当在 EOMA 条件培养基中培养时,Sigmodontis 成虫的存活期也显著延长。总之,这些结果表明 EOMA 产生的因子包括含脂质分子、热不稳定分子(可能是一种蛋白质)以及大小在0.1至1 kDa之间的微量营养素。这些研究建立了一种无细胞方法来在体外长期培养 MF 和成虫期丝虫线虫,并朝着生物化学表征寄生虫存活所需的宿主来源营养物质迈出了重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03dd/5115618/1b161b7f971f/gr1.jpg

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