Chen Xia, Thibeault Susan L
Division of Otolaryngology-Head and Neck Surgery, Department of Surgery, University of Wisconsin-Madison, Madison, Wisconsin 53792-7275, USA.
Laryngoscope. 2008 Sep;118(9):1700-4. doi: 10.1097/MLG.0b013e31817aec6c.
OBJECTIVES/HYPOTHESIS: Normal human vocal fold fibroblast (hVFF) primary cell lines are unavailable commercially and are very difficult to acquire, subsequently little is known about their characteristics. The purpose of this study was to compare the morphological and proliferation characteristics and gene expression of hVFFs from different aged donors.
In vitro.
We developed three normal hVFF primary cell lines from donors aged 21 (21T), 59 (59T) and 79 (79T) years. We characterized their morphological features, proliferative abilities, telomere lengths, and their functional gene expression by quantitative real-time PCR.
The 21T line maintained a typical spindle shape until passage 14 whereas 59T and 79T changed morphology to wider, shorter cells at passage 7. Proliferation rates were constant for the 21T through passage 14; 59T's proliferative half-life was passage 9, whereas 79T maintained lower proliferation rates from passage 4. Gene expression levels for fibronectin, collagen I, collagen VI, procollagen I and elastin demonstrated similar patterns for all lines, however, relative amounts decreased with the age of donor. Telomere lengths did not show differences related with donor age.
hVFF primary cultures have limited proliferative capacity. The morphology, proliferation, differentiation, and gene expression levels of VFF can be affected by age, but senescence patterns were similar across the ages.
目的/假设:正常人类声带成纤维细胞(hVFF)原代细胞系在商业上无法获得且很难获取,因此对其特性了解甚少。本研究的目的是比较不同年龄供体的hVFF的形态、增殖特性和基因表达。
体外研究。
我们从21岁(21T)、59岁(59T)和79岁(79T)的供体中培养出三种正常hVFF原代细胞系。我们通过定量实时PCR对其形态特征、增殖能力、端粒长度及其功能基因表达进行了表征。
21T细胞系在传代14之前保持典型的纺锤形,而59T和79T在传代7时形态变为更宽、更短的细胞。21T细胞系在传代14之前增殖速率恒定;59T的增殖半衰期是传代9,而79T从传代4开始增殖速率较低。纤连蛋白、胶原蛋白I、胶原蛋白VI、前胶原蛋白I和弹性蛋白的基因表达水平在所有细胞系中呈现相似模式,然而,相对含量随供体年龄的增加而降低。端粒长度未显示出与供体年龄相关的差异。
hVFF原代培养物的增殖能力有限。VFF的形态、增殖、分化和基因表达水平会受到年龄的影响,但衰老模式在各年龄段相似。