Researcher, Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Technical Director of the Nordic Reference Laboratory for Genomic Blood Group Typing, Department of Clinical Immunology and Transfusion Medicine, Office of Medical Services, Region Skåne, Sweden.
Immunohematology. 2020 Sep;36(3):99-103.
This update on the P1PK blood group system (Hellberg Å, Westman JS, Thuresson B, Olsson ML. P1PK: the blood group system that changed its name and expanded. Immunohematology 2013;29:25-33) provides recent findings concerning the P1PK blood group system that have both challenged and confirmed old theories. The glycosphingolipids can no longer be considered the sole carriers of the antigens in this system because the P1 antigen has been detected on human red blood cell glycoproteins. New indications suggest that P1Pk synthase activity truly depends on the DXD motif, and the genetic background and molecular mechanism behind the common P1 and P2 phenotypes were found to depend on transcriptional regulation. Transcription factors bind the P1 allele selectively to a motif around rs5751348 in a regulatory region of A4GALT, which enhances transcription of the gene. Nonetheless, unexplained differences in antigen expression between individuals remain.
本关于 P1PK 血型系统的更新(Hellberg Å, Westman JS, Thuresson B, Olsson ML. P1PK:改变名称和扩展的血型系统。免疫血液学 2013;29:25-33)提供了有关 P1PK 血型系统的最新发现,这些发现既挑战了旧理论,也证实了旧理论。糖脂已不再被认为是该系统中抗原的唯一载体,因为已在人红细胞糖蛋白上检测到 P1 抗原。新的迹象表明,P1Pk 合酶活性确实取决于 DXD 基序,而常见的 P1 和 P2 表型背后的遗传背景和分子机制发现取决于转录调控。转录因子选择性地将 P1 等位基因结合到 A4GALT 调节区域中 rs5751348 周围的一个基序上,从而增强基因的转录。尽管如此,个体之间抗原表达的差异仍未得到解释。