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兔泪腺排出道短期阻塞后对泪腺的修复作用。

Lacrimal Gland Repair after Short-term Obstruction of Excretory Duct in Rabbits.

机构信息

Wilmer Eye Institute, School of Medicine, Johns Hopkins University, Baltimore, MD, United States.

Tufts University School of Medicine, Boston, MA, United States.

出版信息

Sci Rep. 2017 Aug 15;7(1):8290. doi: 10.1038/s41598-017-08197-2.

Abstract

Aqueous tear-deficient dry eye is a multifactorial chronic disorder in which the lacrimal glands fail to produce enough tears to maintain a healthy ocular surface. The existence of lacrimal gland stem/progenitor cells was proposed in several species, yet their origin and characteristics are not very clear. Here, we investigated the presence of resident progenitor cells and their regenerative potential in a rabbit model with lacrimal gland main excretory duct ligation-induced injury. The ligation-injured lacrimal glands temporarily decreased in weight and had impaired tear secretion. Protein expression profiles and transcriptional profiles were obtained from injured tissue. Isolated lacrimal gland progenitor cells were tested and characterized by stem cell-related marker evaluation, single cell clonal assay and three-dimensional (3-D) culture. The results of our study indicate that lacrimal glands are capable of tissue repair after duct ligation-induced injury, likely involving resident stem/progenitor cells and epithelial-mesenchymal transitions. Lacrimal gland progenitor cells isolated from ligated tissue can differentiate in 3-D culture. The results provide further insights into lacrimal gland stem/progenitor cell physiology and their potential for treating severe cases of tear deficiency.

摘要

水液性干眼是一种多因素的慢性疾病,泪腺不能产生足够的泪液来维持健康的眼表面。在几种物种中已经提出了泪腺干/祖细胞的存在,但它们的起源和特征尚不清楚。在这里,我们研究了在兔模型中存在的固有祖细胞及其在泪腺主要排泄管结扎诱导损伤后的再生潜力。结扎损伤的泪腺暂时减轻了重量,并且泪液分泌受损。从损伤组织中获得蛋白质表达谱和转录谱。通过干细胞相关标志物评估、单细胞克隆测定和三维(3-D)培养来测试和表征分离的泪腺祖细胞。我们的研究结果表明,泪腺在导管结扎诱导损伤后能够进行组织修复,可能涉及固有干细胞/祖细胞和上皮-间充质转化。从结扎组织中分离的泪腺祖细胞可以在 3-D 培养中分化。这些结果为泪腺干/祖细胞生理学及其治疗严重干眼症的潜力提供了进一步的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef97/5557958/a1893ca7a59b/41598_2017_8197_Fig1_HTML.jpg

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