Poddighe P J, Bulten J, Kerstens H M, Robben J C, Melchers W J, Hanselaar A G
Department of Pathology, University Hospital Nijmegen, The Netherlands.
Clin Mol Pathol. 1996 Dec;49(6):M340-4. doi: 10.1136/mp.49.6.m340.
Aim-To describe a method for amplifying human papilloma virus (HPV) in situ hybridisation (ISH) signals.Methods-Three human cervical cell lines, namely CaSKi, HeLa and SiHa, containing different copy numbers of integrated HPV DNA were studied. Following ISH, catalysed reporter deposition (CARD), based on the deposition of biotinylated tyramine at the location of the DNA probe, was used to amplify the ISH signal.Results-Using CARD-ISH, one to three HPV type 16 copies were detected in situ both in cell suspensions and paraffin wax sections of SiHa cells. CARD-ISH can also be used to detect oncogenic HPV DNA sequences, such as HPV types 16 and 18, in routinely processed formalin fixed, paraffin wax embedded cervical specimens.Conclusions-CARD-ISH is a fast and highly sensitive ISH method for the routine detection of low copy number HPV DNA sequences in cervical cell lines and routinely processed tissue sections. Application of this technology also enables the routine detection and cellular localisation of other viral DNA sequences present at copy numbers below the detection limit of conventional ISH methods.
目的——描述一种放大人类乳头瘤病毒(HPV)原位杂交(ISH)信号的方法。方法——研究了三种含有不同整合HPV DNA拷贝数的人类宫颈细胞系,即CaSKi、HeLa和SiHa。ISH之后,基于生物素化酪胺在DNA探针位置的沉积,采用催化报告沉积法(CARD)放大ISH信号。结果——使用CARD-ISH,在SiHa细胞的细胞悬液和石蜡切片中均原位检测到1至3个HPV 16型拷贝。CARD-ISH还可用于在常规处理的福尔马林固定、石蜡包埋的宫颈标本中检测致癌HPV DNA序列,如HPV 16型和18型。结论——CARD-ISH是一种快速且高度灵敏的ISH方法,用于常规检测宫颈细胞系和常规处理的组织切片中的低拷贝数HPV DNA序列。该技术的应用还能够对拷贝数低于传统ISH方法检测限的其他病毒DNA序列进行常规检测和细胞定位。