• DocumentCode
    3443685
  • Title

    Expression of human fibrinogen in transgenic mice

  • Author

    Subramanian, Anuradha ; Butler, Stephen P. ; Gwazdauskas, Frank C. ; Lubon, Henryk ; Velander, William H.

  • Author_Institution
    Dept. of Chem. Eng., Virginia Polytech. Inst. & State Univ., Blacksburg, VA, USA
  • fYear
    1997
  • fDate
    4-6 Apr 1997
  • Firstpage
    57
  • Lastpage
    60
  • Abstract
    Human fibrinogen (hfib) is a 340 kDa plasma protein which is a complex precursor substrate to fibrin during clot formation. The present work evaluates the potential of the mammary gland of transgenic mice to coordinately express three separate cDNAs for hfib and then assemble hexameric, functional recombinant human fibrinogen (rhfib). Trigenic mice were made by pronuclear co-microinjection of separate constructs for each cDNA of the Aα, Bβ and γ hfib polypeptides. Each transgene contained a 2.6 kb promoter sequence from the murine whey acidic protein (mWAP). Trigenic mice expressing rhfib at about 5-35 μg/ml milk were generated. The rhfib showed an apparent molecular weight by SDS-PAGE similar to that of hfib under non-reducing conditions. Under reducing conditions, the α-chain of rhfib had slightly greater mobility than α-chain from hfib. The rhfib was converted to fibrin by thrombin in a manner similar to that of hfib where a normal fibrin clot and a lower apparent mobility of the α-chain from the clot relative to the starting precursor chains were observed for both rhfib and hfib. In summary, these results show that functional fibrinogen can be synthesized and secreted by the mammary gland of transgenic mice
  • Keywords
    DNA; blood; genetics; molecular biophysics; proteins; α-chain; 340 kDa plasma protein; cDNAs; clot formation; complex precursor substrate; fibrin; hexameric functional recombinant human fibrinogen; human fibrinogen expression; mammary gland; murine whey acidic protein; nonreducing conditions; pronuclear comicroinjection; reducing conditions; transgenic mice; Animals; Assembly; Bioreactors; Humans; Mammary glands; Mice; Nuclear and plasma sciences; Plasma chemistry; Protein engineering; Trigeneration;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Biomedical Engineering Conference, 1997., Proceedings of the 1997 Sixteenth Southern
  • Conference_Location
    Biloxi, MS
  • ISSN
    1086-4105
  • Print_ISBN
    0-7803-3869-3
  • Type

    conf

  • DOI
    10.1109/SBEC.1997.583213
  • Filename
    583213