Matches in SemOpenAlex for { <https://semopenalex.org/work/W2890721701> ?p ?o ?g. }
- W2890721701 endingPage "2257" @default.
- W2890721701 startingPage "2246" @default.
- W2890721701 abstract "Essentials•Mouse models are often used to define roles of tissue factor pathway inhibitor (TFPI) in man.•TFPI isoform‐specific KOs reveal unexpected differences between mouse and human TFPI physiology.•Mouse plasma contains 20 times more TFPI than man, derived from TFPIγ, a form not found in man.•TFPIγ null mice, expressing only TFPI isoforms α and β, may better reflect the human situation.AcknowledgementsWe recognize the Washington University School of Medicine Genomic Engineering and iPC (GEiC) Center for the design and production of the CRISPR reagents and J. M. White and the Pathology Microinjection Core for production of the TFPI exon‐deleted mouse strains. The laboratory of Reed Townsend, Washington University, St. Louis, MO, USA, conducted the tandem MS/MS analyses with support from grants UL1 TR000448 and P41GM103422‐35. Our work was supported by National Institutes of Health grants HL077193 and HL112303.National Institutes of Health HL077193HL112303 UL1 TR000448 P41GM103422‐35Summary: BackgroundMouse models can provide insight into the pathophysiology of human thrombosis and hemostasis. Tissue factor pathway inhibitor (TFPI) regulates coagulation through protein S (PS)‐enhanced factor (F) Xa inhibition and FXa‐dependent inhibition of FVIIa/tissue factor (TF) activity. TFPI is expressed as isoforms α and β in man, and α, β and γ in the mouse.ObjectiveAssess the reliability of extending TFPI‐related studies in mice to humans.MethodCompare mouse and human TFPI physiology using a variety of methods.ResultsMouse TFPI and human TFPI are similar in regard to: (i) the mechanisms for FVIIa/TF and FXa inhibition; (ii) TFPIα is a soluble form and TFPIβ is glycosyl phosphatidyl inositol (GPI) membrane anchored; (iii) the predominant circulating form of TFPI in plasma is lipoprotein‐associated; (iv) low levels of TFPIα circulate in plasma and increase following heparin treatment; and (v) TFPIα is the isoform in platelets. They differ in that: (i) mouse TFPI circulates at a ~20‐fold higher concentration; (ii) mouse lines with isolated isoform deletions show this circulating mouse TFPI is derived from TFPIγ; (iii) sequences homologous to the mouse TFPIγ exon are present in many species, including man, but in primates are unfavorable for splicing; and (iv) tandem mass spectrometry (MS/MS) detects sequences for TFPI isoforms α and β in human plasma and α and γ in mouse plasma.ConclusionTo dissect the pathophysiological roles of human TFPIα and TFPIβ, studies in TFPIγ null mice, expressing only α and β, only α or only β should better reflect the human situation." @default.
- W2890721701 created "2018-09-27" @default.
- W2890721701 creator A5005972807 @default.
- W2890721701 creator A5017018835 @default.
- W2890721701 creator A5040090678 @default.
- W2890721701 creator A5064453044 @default.
- W2890721701 creator A5091457190 @default.
- W2890721701 date "2018-11-01" @default.
- W2890721701 modified "2023-10-14" @default.
- W2890721701 title "Re‐evaluation of mouse tissue factor pathway inhibitor and comparison of mouse and human tissue factor pathway inhibitor physiology" @default.
- W2890721701 cites W139555042 @default.
- W2890721701 cites W145204325 @default.
- W2890721701 cites W1527719951 @default.
- W2890721701 cites W1548350709 @default.
- W2890721701 cites W1549602366 @default.
- W2890721701 cites W1565593572 @default.
- W2890721701 cites W1598671209 @default.
- W2890721701 cites W16018190 @default.
- W2890721701 cites W1603713747 @default.
- W2890721701 cites W1646810589 @default.
- W2890721701 cites W183302857 @default.
- W2890721701 cites W1897287048 @default.
- W2890721701 cites W1974514823 @default.
- W2890721701 cites W1983731186 @default.
- W2890721701 cites W1984814645 @default.
- W2890721701 cites W1988308417 @default.
- W2890721701 cites W1989228194 @default.
- W2890721701 cites W1996636529 @default.
- W2890721701 cites W1996717535 @default.
- W2890721701 cites W1999454666 @default.
- W2890721701 cites W2005970543 @default.
- W2890721701 cites W2012403176 @default.
- W2890721701 cites W2016324820 @default.
- W2890721701 cites W2016846730 @default.
- W2890721701 cites W2020394577 @default.
- W2890721701 cites W2028386603 @default.
- W2890721701 cites W2028554937 @default.
- W2890721701 cites W2029539300 @default.
- W2890721701 cites W2030006942 @default.
- W2890721701 cites W2035405944 @default.
- W2890721701 cites W2037103210 @default.
- W2890721701 cites W2038695690 @default.
- W2890721701 cites W2051035457 @default.
- W2890721701 cites W2056925133 @default.
- W2890721701 cites W2057813521 @default.
- W2890721701 cites W2065168230 @default.
- W2890721701 cites W2068789219 @default.
- W2890721701 cites W2075712620 @default.
- W2890721701 cites W2079470987 @default.
- W2890721701 cites W2087458459 @default.
- W2890721701 cites W2090348276 @default.
- W2890721701 cites W2091903743 @default.
- W2890721701 cites W2094158785 @default.
- W2890721701 cites W2101012337 @default.
- W2890721701 cites W2101123699 @default.
- W2890721701 cites W2107277218 @default.
- W2890721701 cites W2114439064 @default.
- W2890721701 cites W2121114391 @default.
- W2890721701 cites W2135156865 @default.
- W2890721701 cites W2136551871 @default.
- W2890721701 cites W2149648971 @default.
- W2890721701 cites W2160246910 @default.
- W2890721701 cites W2167788545 @default.
- W2890721701 cites W2191656017 @default.
- W2890721701 cites W2192080449 @default.
- W2890721701 cites W2285605960 @default.
- W2890721701 cites W2286978725 @default.
- W2890721701 cites W2399864467 @default.
- W2890721701 cites W2417880428 @default.
- W2890721701 cites W2486241607 @default.
- W2890721701 cites W2583665726 @default.
- W2890721701 cites W2784295509 @default.
- W2890721701 cites W2790442164 @default.
- W2890721701 cites W342996377 @default.
- W2890721701 cites W4235065778 @default.
- W2890721701 cites W4323284335 @default.
- W2890721701 cites W967179082 @default.
- W2890721701 cites W1861626305 @default.
- W2890721701 doi "https://doi.org/10.1111/jth.14288" @default.
- W2890721701 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6235150" @default.
- W2890721701 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30194803" @default.
- W2890721701 hasPublicationYear "2018" @default.
- W2890721701 type Work @default.
- W2890721701 sameAs 2890721701 @default.
- W2890721701 citedByCount "12" @default.
- W2890721701 countsByYear W28907217012019 @default.
- W2890721701 countsByYear W28907217012020 @default.
- W2890721701 countsByYear W28907217012021 @default.
- W2890721701 countsByYear W28907217012022 @default.
- W2890721701 countsByYear W28907217012023 @default.
- W2890721701 crossrefType "journal-article" @default.
- W2890721701 hasAuthorship W2890721701A5005972807 @default.
- W2890721701 hasAuthorship W2890721701A5017018835 @default.
- W2890721701 hasAuthorship W2890721701A5040090678 @default.
- W2890721701 hasAuthorship W2890721701A5064453044 @default.
- W2890721701 hasAuthorship W2890721701A5091457190 @default.
- W2890721701 hasBestOaLocation W28907217011 @default.
- W2890721701 hasConcept C104317684 @default.