Inui Yoshihiro, Nishida Kotaro, Doita Minoru, Takada Toru, Miyamoto Hiroshi, Yoshiya Shinichi, Kurosaka Masahiro
Department of Orthopedic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Spine (Phila Pa 1976). 2004 Nov 1;29(21):2365-9. doi: 10.1097/01.brs.0000143172.07771.fc.
The expression of Fas ligand in the notochord or nucleus pulposus was examined immunohistochemically using rat embryos.
To clarify at which stage of embryo development the expression of Fas ligand begins in the nucleus pulposus.
The nucleus pulposus has been reported to be an immune-privileged site. Immune-privileged characteristics in other tissues, such as the retina and testis, have been attributed to the local expression of Fas ligand, which acts by inducing apoptosis of invading Fas-positive T cells. The authors reported previously on the expression of Fas ligand in nucleus pulposus cells of mature rats and humans, which could play a key role in the potential molecular mechanism of maintaining immune privilege of the disc. However, it is unknown at which stage of the developing embryo Fas ligand expression begins in the nucleus pulposus.
Female adult Sprague-Dawley rats were housed with males for one night and monitored the next morning for the appearance of a vaginal plug. Later, whole sequential embryos were dissected and fixed immediately. Immunohistochemical staining for Fas ligand was performed for sagittal sections of notochords or nucleus pulposus using standard procedures. The sections were observed using light microscopy.
In the 14.5-day-old embryo, the notochord appeared as a continuous structure with a uniform diameter, and there was no positive staining for Fas ligand. In the 16.5-day-old embryo, the notochord became compressed at the centers of the vertebral bodies and expanded in the presumptive nucleus pulposus areas. At this stage, some of the nucleus pulposus cells exhibited weak positive staining for Fas ligand. In the 18.5-day-old embryo, the nucleus pulposus enlarged in fusiform, and most of the nucleus pulposus cells exhibited intense positive staining for Fas ligand.
The present results demonstrated that Fas ligand expression is not detected in the notochord, but at the time of intervertebral disc formation, Fas ligand expression develops in the nucleus pulposus. These results indicate that the immune privilege of the intervertebral disc may begin in the very early stages of disc formation. Moreover, Fas ligand may play an important role in the formation of the intervertebral disc.
使用大鼠胚胎通过免疫组织化学方法检测脊索或髓核中Fas配体的表达。
明确胚胎发育的哪个阶段髓核开始表达Fas配体。
据报道,髓核是一个免疫赦免部位。视网膜和睾丸等其他组织的免疫赦免特性归因于Fas配体的局部表达,Fas配体通过诱导侵入的Fas阳性T细胞凋亡发挥作用。作者之前报道过成熟大鼠和人类髓核细胞中Fas配体的表达,这可能在维持椎间盘免疫赦免的潜在分子机制中起关键作用。然而,尚不清楚在发育中的胚胎的哪个阶段髓核开始表达Fas配体。
成年雌性Sprague-Dawley大鼠与雄性大鼠合笼饲养一晚,次日早晨检查阴道栓的出现情况。之后,解剖整个连续胚胎并立即固定。使用标准程序对脊索或髓核的矢状切片进行Fas配体的免疫组织化学染色。使用光学显微镜观察切片。
在14.5日龄胚胎中,脊索呈现为直径均匀的连续结构,Fas配体无阳性染色。在16.5日龄胚胎中,脊索在椎体中心处受压,并在推测的髓核区域扩张。在此阶段,一些髓核细胞对Fas配体呈弱阳性染色。在18.5日龄胚胎中,髓核呈梭形增大,大多数髓核细胞对Fas配体呈强阳性染色。
目前的结果表明,在脊索中未检测到Fas配体表达,但在椎间盘形成时,髓核中开始出现Fas配体表达。这些结果表明,椎间盘的免疫赦免可能在椎间盘形成的非常早期阶段就开始了。此外,Fas配体可能在椎间盘形成中起重要作用。