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[深圳地区血小板献血者CD36缺陷分子多态性分析]

[Molecular polymorphism Analysis on CD36 Deficiency among Platelet Blood Donors in Shenzhen].

作者信息

Xu Yun-Ping, Sun Ze-Tao, Peng Long, Liang Shuang, Wu Fan, Li Zhen, Li Da-Cheng

机构信息

Shenzhen Blood Center, Institution of Transfusion Medicine, Shenzhen 518035, Guangdong Province, China.

Shenzhen Blood Center, Institution of Transfusion Medicine, Shenzhen 518035, Guangdong Province, China,E-mail:

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2022 Jun;30(3):884-889. doi: 10.19746/j.cnki.issn.1009-2137.2022.03.036.

Abstract

OBJECTIVE

To analyze the molecular polymorphisms of CD36 among 58 blood donors with CD36 deficiency and compare with CD36 positive controls.

METHODS

A total of 58 donors with CD36 deficiency during a screening conducted in the laboratory from September 2019 to December 2020 were enrolled as the test group, including 39 males and 19 females, while 120 platelet donors with CD36 positive were randomly selected as the controls, including 76 males and 44 females. All of the subjects were Han nationality. The PCR-SBT method was used to detect coding region of CD36 gene, and molecular mutations were compared with those CD36 positive controls.

RESULTS

Among the 58 donors with CD36 deficiency, mutations appears in 32 individuals. The detection rate for type I was 71.43% (5/7), and type II was 51.92% (27/52), while among the 120 controls, mutations appears in 12 donors (10%). In the CD36 antigen-deficient donors, 16 variations were found, in which 329-330 del AC with the highest frequency accounted for 20.69%, followed by 1228-1239 del ATTGTGCCTATT(15.52%) and 1156 C>T(10.34%). Two variations, 198-205 del GATCTTTG and 220 C>T, led to premature termination of translation; four mutations, 329-330 del AC, 560 ins T, 1011-1049 39bp dupl and 1343-1344 ins TCTT, caused translation frame shift; 1228-1239 del ATTGTGCCTATT led to deletion of four amino acids (Ile-Val-Pro-Ile) at sites 410-413 of the peptide chain. The 1140 T>A and 1275 G>A were synonymous mutations, and the other 7 mutations resulted in the substitution of single nucleotide. The platelet expression in the donors of CD36 positive with 329-330 del AC or 1228-1239 del ATTGTGCCTATT mutation (heterozygote) was lower than those CD36 positive individuals without mutations (homozygote).

CONCLUSION

Multiple gene mutations in the CD36 coding region may cause CD36 deficiency, and the heterozygous individuals with mutations may lead to CD36 antigen reduction or deletion. Mutation is not detected in 44.83% of CD36 deficient individuals, there may be some other reasons for the CD36 antigen deficiency.

摘要

目的

分析58例CD36缺陷献血者的CD36分子多态性,并与CD36阳性对照进行比较。

方法

选取2019年9月至2020年12月实验室筛查出的58例CD36缺陷献血者作为试验组,其中男性39例,女性19例;随机选取120例CD36阳性的血小板献血者作为对照组,其中男性76例,女性44例。所有受试者均为汉族。采用PCR-SBT法检测CD36基因编码区,并与CD36阳性对照比较分子突变情况。

结果

58例CD36缺陷献血者中,32例出现突变。Ⅰ型检出率为71.43%(5/7),Ⅱ型为51.92%(27/52);120例对照组中,12例(10%)出现突变。在CD36抗原缺陷献血者中,发现16种变异,其中频率最高的329-330 del AC占20.69%,其次为1228-1239 del ATTGTGCCTATT(15.52%)和1156 C>T(10.34%)。198-205 del GATCTTTG和220 C>T这两种变异导致翻译提前终止;329-330 del AC、560 ins T、1011-1049 39bp dupl和1343-1344 ins TCTT这4种突变导致翻译移码;1228-1239 del ATTGTGCCTATT导致肽链410-413位缺失4个氨基酸(Ile-Val-Pro-Ile)。1140 T>A和1275 G>A为同义突变,其余7种突变为单核苷酸替换。329-330 del AC或1228-1239 del ATTGTGCCTATT突变(杂合子)的CD36阳性献血者血小板表达低于无突变的CD36阳性个体(纯合子)。

结论

CD36编码区的多个基因突变可能导致CD36缺陷,突变杂合子个体可能导致CD36抗原减少或缺失。44.83%的CD36缺陷个体未检测到突变,CD36抗原缺陷可能存在其他原因。

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