Maternal fibrinogen is necessary for embryonic development

被引:32
作者
Iwaki, T [1 ]
Castellino, FJ [1 ]
机构
[1] Univ Notre Dame, WM Keck Ctr Transgene Res, Dept Chem & Biochem, Notre Dame, IN 46556 USA
关键词
fibrinogen deficiency; pregnancy; spontaneous miscarriage; embryonic development;
D O I
10.2174/1389450054546006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fibrinogen (Fg) is a precursor of fibrin, which is one of the main components of blood clots generated during the hemostatic response. Beyond its important role in hemostasis, Fg is involving in several physiologic and pathophysiologic states, such as infection, wound healing, the progression of certain types of tumors, and the severity of atherosclerosis. In addition, Fg has a critical role in maintaining pregnancy. Ovulation, fertilization, and implantation of the fertilized egg to the uterine wall can occur in afibrinogenemic women. However, all pregnancies in these patients resulted in spontaneous miscarriage. Fg supplemental therapy allows the patients to sustain the pregnancy. Mice with a total fibrinogen deficiency (FG(-)) reproduce the human experience. Despite of successes with fibrinogen supplementation. "paradoxical thrombosis" sometimes occurs, wherein supplemental therapies cause catastrophic thrombosis, such as pulmonary and mesenteric venous thrombosis. In these therapies, syncytial knots, hyaline membrane, and multiple recent infarctions with abruptio placenta were also observed. These findings indicate that the dosage regimen of Fg in afibrinogenemia-related pregnancies needs to be optimized according to other coagulation markers, such as thrombin-antithrombin complex (TAT) concentration, which represents the extent of thrombin formation. In addition, baseline thrombin assays would be helpful to predict the potential for paradoxical thrombosis during the supplemental therapy offered during pregnancy.
引用
收藏
页码:535 / 539
页数:5
相关论文
共 53 条
[1]   CONGENITAL AFIBRINOGENEMIA [J].
ALMONDHIRY, H ;
EHMANN, WC .
AMERICAN JOURNAL OF HEMATOLOGY, 1994, 46 (04) :343-347
[2]   Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation [J].
Asselta, R ;
Duga, S ;
Simonic, T ;
Malcovati, M ;
Santagostino, E ;
Giangrande, PLF ;
Mannucci, PM ;
Tenchini, ML .
BLOOD, 2000, 96 (07) :2496-2500
[3]   Congenital afibrinogenemia:: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs [J].
Asselta, R ;
Duga, S ;
Spena, S ;
Santagostino, E ;
Peyvandi, F ;
Piseddu, G ;
Targhetta, R ;
Malcovati, M ;
Mannucci, PM ;
Tenchini, ML .
BLOOD, 2001, 98 (13) :3685-3692
[4]  
BOTTINI E, 1991, HAEMATOLOGICA, V76, P431
[5]   THE ROLE OF FIBRIN IN TUMOR-METASTASIS [J].
COSTANTINI, V ;
ZACHARSKI, LR .
CANCER AND METASTASIS REVIEWS, 1992, 11 (3-4) :283-290
[6]   Genetic insights into trophoblast differentiation and placental morphogenesis [J].
Cross, JC .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2000, 11 (02) :105-113
[7]   VONWILLEBRAND-FACTOR INTERACTION WITH THE GLYCOPROTEIN-IIB GLYCOPROTEIN-IIIA COMPLEX - ITS ROLE IN PLATELET-FUNCTION AS DEMONSTRATED IN PATIENTS WITH CONGENITAL AFIBRINOGENEMIA [J].
DEMARCO, L ;
GIROLAMI, A ;
ZIMMERMAN, TS ;
RUGGERI, ZM .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (04) :1272-1277
[8]   FIBRINOGEN AND FIBRIN [J].
DOOLITTLE, RF .
ANNUAL REVIEW OF BIOCHEMISTRY, 1984, 53 :195-229
[9]   CONGENITAL DEFICIENCY OF FIBRINOGEN IN 2 SISTERS - A CLINICAL AND HAEMATOLOGICAL STUDY [J].
DUBE, B ;
AGARWAL, SP ;
GUPTA, MM ;
CHAWLA, SC .
ACTA HAEMATOLOGICA, 1970, 43 (02) :120-&
[10]   Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion [J].
Duga, S ;
Asselta, R ;
Santagostino, E ;
Zeinali, S ;
Simonic, T ;
Malcovati, M ;
Mannucci, PM ;
Tenchini, ML .
BLOOD, 2000, 95 (04) :1336-1341