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Characterization of cryopreserved primary human corneal endothelial cells cultured in human serum-supplemented media

机译:在人血清补充培养基中培养的冷冻保存的原代人角膜内皮细胞的特性

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Purpose: To compare cryopreserved human corneal endothelial cells (HCECs) grown in human serum-supplemented media (HS-SM) with cryopreserved HCECs grown in fetal bovine serum-supplemented media (FBS-SM). Methods: Three pairs of human corneas from donors aged 8, 28, and 31 years were obtained from the eye bank. From each pair, one cornea was used to start a HCEC culture using HS-SM; the other cornea was grown in FBS-SM. On reaching confluence, the six cell populations were frozen using 10% dimethyl sulfoxidecontaining medium. Thawed cells grown in HS-SM were compared with those grown in FBS-SM with respect to morphology, growth curves, immunohistochemistry, real time-reverse transcriptase polymerase chain reaction (RT-PCR) for endothelial cell markers, and detachment time. Results: No difference in morphology was observed for cells grown in the two media before or after cryopreservation. By growth curves, cell counts after thawing were similar in both media, with a slight trend toward higher cell counts in FBS-SM. Cells grown in both the media demonstrated a similar expression of endothelial cell markers when assessed by immunohistochemistry, although HCEC marker gene expression was higher in cells grown in HS-SM than in those grown in FBS-SM as assessed by RT-PCR. With FBS-SM, there was a tendency of longer detachment time and lower cell passages. Conclusions: HS-SM was similar to FBS-SM for cryopreservation of cultured HCECs as assessed by analysis of cell morphology, proliferation, and protein expression, although marker gene expression was higher in cells grown in HS-SM than in those grown in FBS-SM. Detachment time was longer with FBS-SM and in lower passages.
机译:目的:比较在人血清补充培养基(HS-SM)中生长的冷冻保存的人角膜内皮细胞(HCEC)与在胎牛血清补充培养基(FBS-SM)中生长的冷冻保存的HCEC。方法:从眼库中获得三对分别来自年龄分别为8、28和31岁的供体的人角膜。从每对中,一个角膜用于使用HS-SM启动HCEC培养;另一个角膜生长在FBS-SM中。达到汇合后,使用10%含二甲基亚砜的培养基冷冻六个细胞群。将HS-SM中融化的细胞与FBS-SM中融化的细胞的形态,生长曲线,免疫组织化学,实时逆转录酶聚合酶链反应(RT-PCR)用于内皮细胞标记物以及分离时间进行了比较。结果:在冷冻保存之前或之后,两种培养基中生长的细胞在形态上均未观察到差异。通过生长曲线,两种培养基在融化后的细胞数相似,在FBS-SM中细胞数略有增加的趋势。通过免疫组织化学评估时,两种培养基中生长的细胞均表现出相似的内皮细胞标记物表达,尽管通过RT-PCR评估,HS-SM中生长的细胞中HCEC标记基因表达高于FBS-SM中生长的细胞。使用FBS-SM,存在更长的分离时间和更低的细胞通过率的趋势。结论:通过细胞形态,增殖和蛋白质表达分析评估,HS-SM与FBS-SM在冷冻培养的HCEC的冷冻保存方面相似,尽管HS-SM中生长的细胞中标记基因的表达高于FBS-SM中生长的细胞。 SM。 FBS-SM和较低通道的拆卸时间更长。

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