کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6155829 | 1597940 | 2016 | 43 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Search for the potential “second-hit” mechanism underlying the onset of familial hemophagocytic lymphohistiocytosis type 2 by whole-exome sequencing analysis
ترجمه فارسی عنوان
جستجو برای پتانسیل دوم هیتا مکانیزمی که مبتنی بر شروع نوع دوم لنفوهیستسیتوزیس هموفاگوسیتیسم خانوادگی است با تجزیه و تحلیل توالی آمیزشی کامل
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کلمات کلیدی
PBSHLHRT-PCRcytotoxic T cellsAPCrIL-2PRF1PBMCsFHLCTLs - CTL هاH&E - H & Eantigen-presenting cell - آنتیژن ارائه سلولEBV - اپشتین بار ویروسrecombinant interleukin 2 - اینترلوکین نوترکیب 2standard error - خطای استانداردperipheral blood mononuclear cells - سلول های تک هسته ای خون محیطیHemophagocytic lymphohistiocytosis - لنفوهیستسیتوز هموفوگوسیتیکfamilial hemophagocytic lymphohistiocytosis - لنفوهیستسیتوزیس هموفاگوسیتیسم خانوادگیHematoxylin and Eosin - هماتوکسیلین و ائوزینreverse transcription–polymerase chain reaction - واکنش زنجیره ای رونویسی-پلیمراز معکوسEpstein-Barr virus - ویروس Epstein-Barr
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
پزشکی و دندانپزشکی (عمومی)
چکیده انگلیسی
Familial hemophagocytic lymphohistiocytosis type 2 (FHL2), caused by perforin 1 (PRF1), is a genetic disorder of lymphocyte cytotoxicity that usually presents in the first 2Â years of life and has a poor prognosis. Late onset of FHL2 has been sporadically reported, and the mechanism is largely unknown. A newly diagnosed FHL2 patient was detected to have compound mutations in both PRF1 alleles and positive Epstein-Barr virus (EBV) infection. Her brother carried the same mutations and EBV infection status but kept healthy. To search the potential unknown mechanisms, we performed whole-exome sequencing analysis. The patient and her asymptomatic brother carried the same heterozygous missense (c.916G>A) and frameshift mutation (c.65delC) in PRF1. Germline mutation analysis demonstrated that only the proband was exclusively detected with a homozygous missense mutation (S1006L) in the PCDH18 gene, whereas others were found to have a heterozygous mutation (S1006L) of PCDH18. The calculated stability (free energy) changes showed that the mutation of PCDH18 mainly destabilized the protein structure. Furthermore, the mutation (S1006L) could lessen the PCDH18-induced inhibition of target cell activation and reduce the apoptosis of T lymphocytes. This study is the first to perform whole-exome sequencing analysis to search the potential “second-hit” mechanism that underlies the onset of FHL2. A novel type of compound heterozygous mutation has been found in PRF1. The detection of the homozygous germline mutation in PCDH18 strongly argues that the presence of a “second” germline mutation besides the PRF1 gene might be potentially an important mechanism for triggering the onset of FHL2.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Translational Research - Volume 170, April 2016, Pages 26-39
Journal: Translational Research - Volume 170, April 2016, Pages 26-39
نویسندگان
Lili Gao, Xiao Dang, Liang Huang, Li Zhu, Mingyan Fang, Jianguo Zhang, Xun Xu, Lijun Zhu, Tongjuan Li, Lei Zhao, Jia Wei, Jianfeng Zhou,