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Related Concept Videos

Fibronectins Connect Cells with ECM01:25

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Fibronectin is an adhesive glycoprotein present in the extracellular matrix of embryogenic and adult tissue. These molecules primarily aid in regulating cell motility and attachment. A fibronectin molecule is composed of two identical polypeptide chains attached to each other by a pair of disulfide bonds at the C-terminal.
Both proteoglycans and collagen are attached to fibronectin proteins, which, in turn, are attached to integrin proteins. These integrin proteins interact with transmembrane...
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Related Experiment Video

Updated: May 5, 2026

FIBS-enabled Noninvasive Metabolic Profiling
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Human fibronectin metabolism.

B A Pussell, P W Peake, M A Brown

    The Journal of Clinical Investigation
    |July 1, 1985
    PubMed
    Summary
    This summary is machine-generated.

    Fibronectin (Fn) deficiency in critically ill patients is primarily due to reduced synthesis, not increased breakdown or distribution. This finding impacts understanding of critical illness-related protein metabolism.

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    Area of Science:

    • Biochemistry
    • Physiology
    • Critical Care Medicine

    Background:

    • Fibronectin (Fn) is a crucial adhesive glycoprotein involved in cell adhesion and matrix formation.
    • Understanding Fn's metabolic behavior is vital for comprehending its role in health and disease, particularly in critical illness.

    Purpose of the Study:

    • To investigate the metabolic fate of fibronectin (Fn) in healthy individuals and critically ill patients.
    • To determine the factors contributing to low plasma Fn levels observed in critical illness.

    Main Methods:

    • Human plasma fibronectin (Fn) was purified and radiolabeled.
    • Metabolic parameters including fractional catabolic rate (FCR), half-life (t1/2), extravascular/intravascular diffusion ratio (EV/IV), and synthesis rate (SR) were measured in eight healthy controls and 11 patients (six critically ill).

    Main Results:

    • In healthy controls, Fn exhibited rapid catabolism with a fractional catabolic rate (FCR) of 4.81%/h and a half-life (t1/2) of 25 hours.
    • Critically ill patients showed a lower EV/IV ratio, and those with low plasma Fn had markedly depressed synthesis rates (SR).
    • Plasma Fn levels correlated with SR but not with t1/2 or FCR.

    Conclusions:

    • Reduced synthesis of fibronectin (Fn), not increased catabolism or distribution, is the primary cause of Fn deficiency in critically ill patients.
    • These findings highlight the importance of synthesis in maintaining adequate Fn levels during critical illness.