Budimlija Zoran M, Lechpammer Mirna, Popiolek Dorota, Fogt Franz, Prinz Mechthild, Bieber Frederick R
Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.
Croat Med J. 2005 Aug;46(4):549-55.
To report on the successful use of Laser Capture Microdissection (LCM) as a tool for isolation of human chorionic villi from admixed maternal tissue. Subsequent DNA isolation for forensic short tandem repeat (STR) analysis for parentage testing was performed in two cases of alleged sexual assault of female victims. We also performed validation of the LCM instrument platform, using archival formalin-fixed human fetal products of conception (POC), for which microdissection was utilized to separate maternal (decidua) and fetal (chorionic villus) components.
To isolate DNA from placental chorionic villi admixed with maternal decidua recovered after spontaneous or therapeutic abortion, LCM was used to separate fetal from maternal cells. In contrast to the relatively crude conventional microdissection performed using a narrow pipette, needle, or scalpel blade, LCM allows cell- or tissue-specific isolation of placental chorionic villi from archival paraffin-embedded tissue sections, leaving the maternal tissue intact.
After polymerase chain reaction (PCR) amplification of villi after LCM of 9-15 STR loci, the quantity and quality of DNA yielded from fetal cells isolated by LCM was sufficient for PCR analysis and successful forensic parentage testing. The validation data obtained on two sets of formalin-fixed archival POC tissues from anonymous donors demonstrated the encouraging reproducibility of these protocols and procedures.
We demonstrated the reliability and utility of LCM for forensic applications when high specificity of a particular analyzed cell population or tissue is required. Care must be taken during routine pathology procedures to avoid contamination of tissues with admixture of extraneous DNA.
报告成功使用激光捕获显微切割技术(LCM)从混杂的母体组织中分离人绒毛膜绒毛的情况。在两起女性受害者涉嫌性侵犯案件中,对分离出的绒毛进行后续DNA提取,用于法医短串联重复序列(STR)分析以进行亲子鉴定。我们还使用存档的福尔马林固定的人胎儿妊娠产物(POC)对LCM仪器平台进行了验证,利用显微切割分离母体(蜕膜)和胎儿(绒毛膜绒毛)成分。
为了从自然流产或治疗性流产后回收的与母体蜕膜混合的胎盘绒毛膜绒毛中分离DNA,使用LCM将胎儿细胞与母体细胞分离。与使用狭窄移液管、针或手术刀刀片进行的相对粗糙的传统显微切割不同,LCM允许从存档石蜡包埋组织切片中细胞或组织特异性分离胎盘绒毛膜绒毛,而母体组织保持完整。
对9 - 15个STR位点进行LCM后的绒毛进行聚合酶链反应(PCR)扩增后,LCM分离出的胎儿细胞产生的DNA数量和质量足以进行PCR分析和成功的法医亲子鉴定。从匿名捐赠者的两组福尔马林固定存档POC组织获得的验证数据证明了这些方案和程序令人鼓舞的可重复性。
我们证明了在需要特定分析细胞群体或组织的高特异性时,LCM在法医应用中的可靠性和实用性。在常规病理程序中必须小心,以避免组织被外来DNA污染。