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Tight Junctions / by Lorenza Gonzalez-Mariscal

By: Gonzalez-Mariscal, Lorenza
Material type: materialTypeLabelE-bookPublisher: Boston, MA : Springer International Publishing, 2006Description: 1 recurso en línea (XI, 224 p.).ISBN: 9780387366739.Subject: CitologíaOnline resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources Summary: ight junctions (TJs) are cell-ceil adhesion belts that encircle epithelial and endothelial cells at the limit between the apical and the lateral Tmembrane. These junctions are crucial for the establishment of separate compartments in multicellular organisms and for the exchange of substances between the internal milieu and the external environment. The perception of TJs has changed over the years. From being regarded as static paracellular seals, they have come to be perceived as dynamic structures that adjust their morpholÂ{u0BE7}y and function in response to physiological, pharmacological and pathologiÂ{u08E1}l challenges. The roles that TJs play in epithelial and endothelial cells has also widened, and nowadays this structure is regarded not only as a fence that limits within the membrane, the movement of proteins and lipids between the apical and basolateral membranes, or as a gate that regulates in a size and charge selecÂ{u0D29}ve manner the transit of ion and molecules through the paracellular pathway, but also as a structure integrated by molecules that participate in the control of cell proliferation. These observations highlight the importance of understandÂ{u0A6E}g TJ physiology in order to develop effective strategies for the treatment of pathological conditions such as cancer and autoimmune diseases. This broader perception of TJs is reflected in all the chapters of the book and has been attained thanks to the identification in recent years of a wide array of proteins that constitute TJs in epithelial and endothelial cells as well as in central nervous system myelin.
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Item type Current library Collection Call number Copy number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud QH603.C4 G669 2006 EB (Browse shelf(Opens below)) .i11542512 Acceso electrónico eBOOK .i11542512
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QH603 .A98 2016 EB Autophagy Networks in Inflammation QH603.C4 2022 EB Tight Junctions QH603.C4 B358 2006 EB Cell-Cell Channels QH603.C4 G669 2006 EB Tight Junctions QH603.C43 1997 EB Receptor Signal Transduction Protocols QH603 .C43 2004 EB Receptor Signal Transduction Protocols QH603 .C43 2011 EB Receptor Signal Transduction Protocols : Third Edition

ight junctions (TJs) are cell-ceil adhesion belts that encircle epithelial and endothelial cells at the limit between the apical and the lateral Tmembrane. These junctions are crucial for the establishment of separate compartments in multicellular organisms and for the exchange of substances between the internal milieu and the external environment. The perception of TJs has changed over the years. From being regarded as static paracellular seals, they have come to be perceived as dynamic structures that adjust their morpholÂ{u0BE7}y and function in response to physiological, pharmacological and pathologiÂ{u08E1}l challenges. The roles that TJs play in epithelial and endothelial cells has also widened, and nowadays this structure is regarded not only as a fence that limits within the membrane, the movement of proteins and lipids between the apical and basolateral membranes, or as a gate that regulates in a size and charge selecÂ{u0D29}ve manner the transit of ion and molecules through the paracellular pathway, but also as a structure integrated by molecules that participate in the control of cell proliferation. These observations highlight the importance of understandÂ{u0A6E}g TJ physiology in order to develop effective strategies for the treatment of pathological conditions such as cancer and autoimmune diseases. This broader perception of TJs is reflected in all the chapters of the book and has been attained thanks to the identification in recent years of a wide array of proteins that constitute TJs in epithelial and endothelial cells as well as in central nervous system myelin.

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