Department of Histology and Embryology, Akdeniz University School of Medicine, Antalya, Turkey.
Department of Histology and Embryology, Akdeniz University School of Medicine, Antalya, Turkey; Department of Obstetrics, Gynecology and Reproductive Sciences, Center for Reproductive Sciences, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California San Francisco, San Francisco, CA, USA.
Tissue Cell. 2021 Oct;72:101528. doi: 10.1016/j.tice.2021.101528. Epub 2021 Mar 16.
CTCFL is expressed in testis, oocytes and embryonic stem cells, and is aberrantly expressed in malignant cells, and is classified as a cancer-testis gene. We have previously shown by using a tetracycline-inducible Ctcfl transgene that inappropriate expression of Ctcfl negatively impacts fetal development and causes early postnatal lethality in the mouse. The affected pups displayed severe vascular abnormalities and localized hemorrhages in the brain evocative of cerebral cavernous malformations (CCM) and arteriovenous malformations (AVM) in humans. Thus, we aim to analyze; a) the presence of CCM-related proteins CCM1/KRIT1, CCM2/malcavernin and CCM3/PDCD10 in Ctcfl transgenic animals and, b) whether there is CTCFL expression in human CCM and AVM tissues. Ctcfl transgenic animals exhibited increased CD31 expression in vascular areas of the dermis and periadnexal regions but no difference was observed for vWF and α-SMA expressions. CCM-related proteins CCM1/KRIT1, CCM2/malcavernin and CCM3/PDCD10 were aberrantly expressed in coronal sections of the head in transgenic animals. We also observed CTCFL expression in human CCMs and AVMs. The induced expression of CTCFL resulting in vascular brain malformations in mice combined with the presence of CTCFL in human vascular malformations provide new insights into the role of this gene in vascular development in humans.
CTCFL 在睾丸、卵子和胚胎干细胞中表达,在恶性细胞中异常表达,并被归类为癌症-睾丸基因。我们之前通过使用四环素诱导的 Ctcfl 转基因,证明了 Ctcfl 的不当表达会对胎儿发育产生负面影响,并导致小鼠出生后早期死亡。受影响的幼鼠表现出严重的血管异常和大脑局部出血,类似于人类的脑海绵状血管畸形 (CCM) 和动静脉畸形 (AVM)。因此,我们旨在分析:a)CCM 相关蛋白 CCM1/KRIT1、CCM2/malcavernin 和 CCM3/PDCD10 在 Ctcfl 转基因动物中的存在情况,以及 b) CTCFL 是否在人类 CCM 和 AVM 组织中表达。Ctcfl 转基因动物的皮肤真皮和附属区域的血管区域中 CD31 表达增加,但 vWF 和 α-SMA 表达没有差异。CCM 相关蛋白 CCM1/KRIT1、CCM2/malcavernin 和 CCM3/PDCD10 在转基因动物的头部冠状切片中异常表达。我们还观察到 CTCFL 在人类 CCM 和 AVM 中的表达。CTCFL 的诱导表达导致小鼠的血管性脑畸形,加上 CTCFL 存在于人类血管畸形中,为该基因在人类血管发育中的作用提供了新的见解。