Department of Medical Sciences, Graduate School of Medicine, Science and Technology, Shinshu University, Matsumoto 390-8621, Japan.
Department of Laboratory Medicine, Shinshu University Hospital, Matsumoto 390-8621, Japan.
Int J Mol Sci. 2021 May 14;22(10):5218. doi: 10.3390/ijms22105218.
We identified a novel heterozygous hypofibrinogenemia, γY278H (Hiroshima). To demonstrate the cause of reduced plasma fibrinogen levels (functional level: 1.12 g/L and antigenic level: 1.16 g/L), we established γY278H fibrinogen-producing Chinese hamster ovary (CHO) cells. An enzyme-linked immunosorbent assay demonstrated that synthesis of γY278H fibrinogen inside CHO cells and secretion into the culture media were not reduced. Then, we established an additional five variant fibrinogen-producing CHO cell lines (γL276P, γT277P, γT277R, γA279D, and γY280C) and conducted further investigations. We have already established 33 γ-module variant fibrinogen-producing CHO cell lines, including 6 cell lines in this study, but only the γY278H and γT277R cell lines showed disagreement, namely, recombinant fibrinogen production was not reduced but the patients' plasma fibrinogen level was reduced. Finally, we performed fibrinogen degradation assays and demonstrated that the γY278H and γT277R fibrinogens were easily cleaved by plasmin whereas their polymerization in the presence of Ca and "D:D" interaction was normal. In conclusion, our investigation suggested that patient γY278H showed hypofibrinogenemia because γY278H fibrinogen was secreted normally from the patient's hepatocytes but then underwent accelerated degradation by plasmin in the circulation.
我们鉴定了一种新型杂合子低纤维蛋白原血症,γY278H(广岛)。为了证明血浆纤维蛋白原水平降低的原因(功能水平:1.12 g/L,抗原水平:1.16 g/L),我们建立了γY278H 纤维蛋白原产生的中国仓鼠卵巢(CHO)细胞。酶联免疫吸附试验表明,CHO 细胞内 γY278H 纤维蛋白原的合成和分泌到培养基中没有减少。然后,我们建立了另外五个变体纤维蛋白原产生的 CHO 细胞系(γL276P、γT277P、γT277R、γA279D 和 γY280C)并进行了进一步的研究。我们已经建立了 33 个 γ 模块变体纤维蛋白原产生的 CHO 细胞系,包括本研究中的 6 个细胞系,但只有γY278H 和γT277R 细胞系表现出不一致,即重组纤维蛋白原的产生没有减少,但患者的血浆纤维蛋白原水平降低。最后,我们进行了纤维蛋白原降解试验,证明γY278H 和γT277R 纤维蛋白原容易被纤溶酶裂解,而它们在 Ca 和“D:D”相互作用存在下的聚合是正常的。总之,我们的研究表明,患者γY278H 表现出低纤维蛋白原血症,因为γY278H 纤维蛋白原正常从患者的肝细胞分泌,但随后在循环中被纤溶酶加速降解。