Xiao Jingnan, Natarajan Kanchana, Rajala Maitreyi S, Astley Roger A, Ramadan Raniyah T, Chodosh James
Molecular Pathogenesis of Eye Infection Research Center, Dean A. McGee Eye Institute, Department of Ophthalmology, University of Oklahoma Health Sciences Center, 608 Stanton L. Young Boulevard, Oklahoma City, OK 73104, USA.
Am J Ophthalmol. 2005 Sep;140(3):363-9. doi: 10.1016/j.ajo.2005.03.077.
Adenoviruses typically demonstrate specific tissue tropisms, as in the association of Ad19 with epidemic keratoconjunctivitis. We sought to determine factors that might influence the apparent tropism of Ad19 for the cornea.
Laboratory investigation.
Adenovirus serotypes Ad2, 5, 9, 10, 11, 13, and 19 were compared for their capacity to replicate in human corneal epithelial cells (HCECs) in culture. Organotypically cultured human corneas were infected with Ad19 or Ad2, and viral titers were compared after 7 days. Replication of both viruses was compared in HCECs cultured on various extracellular matrices. Western blot analysis and immunohistochemistry were applied to human donor corneas and HCECs.
One week after infection of HCEC monolayer cultures, Ad2 titers were significantly higher than any of the other viruses tested (P <.05). In organotypic corneal cultures, Ad19 titers were significantly higher than Ad2 (P = .0003). Ad2 replication in HCECs equaled or exceeded that of Ad19 on all extracellular matrices except vitronectin, where Ad2 replication was reduced and Ad19 replication enhanced (P <.0001). Vitronectin was detected by immunohistochemistry within the corneal epithelial basement membranes of human donor corneas. Increased alpha(v) integrin expression and greater tyrosine kinase phosphorylation in HCECs cultured on vitronectin were demonstrated by Western blot analysis.
In vitro, vitronectin enhances growth of Ad19, possibly by up-regulation of receptor alpha(v) integrins and increased activity of tyrosine kinases necessary for adenoviral internalization. We hypothesize that differential tissue tropisms for adenoviruses may derive in part from tissue-specific extracellular matrix expression.
腺病毒通常表现出特定的组织嗜性,如Ad19与流行性角结膜炎的关联。我们试图确定可能影响Ad19对角膜明显嗜性的因素。
实验室研究。
比较腺病毒血清型Ad2、5、9、10、11、13和19在培养的人角膜上皮细胞(HCECs)中的复制能力。用Ad19或Ad2感染器官型培养的人角膜,7天后比较病毒滴度。比较两种病毒在各种细胞外基质上培养的HCECs中的复制情况。对人供体角膜和HCECs进行蛋白质印迹分析和免疫组织化学检测。
感染HCEC单层培养物1周后,Ad2滴度显著高于其他任何测试病毒(P<.05)。在器官型角膜培养中,Ad19滴度显著高于Ad2(P =.0003)。在除玻连蛋白外的所有细胞外基质上,HCECs中Ad2的复制等于或超过Ad19,在玻连蛋白上Ad2复制减少而Ad19复制增强(P<.0001)。通过免疫组织化学在人供体角膜的角膜上皮基底膜内检测到玻连蛋白。蛋白质印迹分析表明,在玻连蛋白上培养的HCECs中α(v)整合素表达增加且酪氨酸激酶磷酸化增强。
在体外,玻连蛋白可能通过上调受体α(v)整合素和增加腺病毒内化所需的酪氨酸激酶活性来促进Ad19的生长。我们推测腺病毒不同的组织嗜性可能部分源于组织特异性细胞外基质的表达。