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Identification of Novel Equine ( Equus caballus ) Tendon Markers Using RNA Sequencing

机译:使用RNA序列鉴定新型马(马)肌腱标记。

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Although several tendon-selective genes exist, they are also expressed in other musculoskeletal tissues. As cell and tissue engineering is reliant on specific molecular markers to discriminate between cell types, tendon-specific genes need to be identified. In order to accomplish this, we have used RNA sequencing (RNA-seq) to compare gene expression between tendon, bone, cartilage and ligament from horses. We identified several tendon-selective gene markers, and established eyes absent homolog 2 ( EYA2 ) and a G-protein regulated inducer of neurite outgrowth 3 ( GPRIN3 ) as specific tendon markers using RT-qPCR. Equine tendon cells cultured as three-dimensional spheroids expressed significantly greater levels of EYA2 than GPRIN3 , and stained positively for EYA2 using immunohistochemistry. EYA2 was also found in fibroblast-like cells within the tendon tissue matrix and in cells localized to the vascular endothelium. In summary, we have identified EYA2 and GPRIN3 as specific molecular markers of equine tendon as compared to bone, cartilage and ligament, and provide evidence for the use of EYA2 as an additional marker for tendon cells in vitro.
机译:尽管存在几种腱选择基因,但它们也在其他肌肉骨骼组织中表达。由于细胞和组织工程依赖于特定的分子标记来区分细胞类型,因此需要鉴定肌腱特异性基因。为此,我们使用RNA测序(RNA-seq)来比较马的肌腱,骨骼,软骨和韧带之间的基因表达。我们鉴定了几种腱选择基因标记,并建立了不存在同源物2(EYA2)和神经突增生3(GPRIN3)的G蛋白调节诱导剂的眼睛,作为使用RT-qPCR的特定腱标记。培养成三维球体的马腱细胞表达的EYA2水平明显高于GPRIN3,并且使用免疫组织化学法对EYA2染色呈阳性。在肌腱组织基质内的成纤维细胞样细胞以及位于血管内皮的细胞中也发现了EYA2。总之,与骨骼,软骨和韧带相比,我们已将EYA2和GPRIN3确定为马肌腱的特定分子标记,并为使用EYA2作为体外肌腱细胞的其他标记提供了证据。

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