PMC:6194691 / 45013-45954 JSONTXT

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    MyTest

    {"project":"MyTest","denotations":[{"id":"30340614-20468051-30706066","span":{"begin":564,"end":567},"obj":"20468051"},{"id":"30340614-20468051-30706067","span":{"begin":674,"end":677},"obj":"20468051"},{"id":"30340614-27799072-30706068","span":{"begin":938,"end":939},"obj":"27799072"}],"namespaces":[{"prefix":"_base","uri":"https://www.uniprot.org/uniprot/testbase"},{"prefix":"UniProtKB","uri":"https://www.uniprot.org/uniprot/"},{"prefix":"uniprot","uri":"https://www.uniprot.org/uniprotkb/"}],"text":"The blood–brain barrier is more selective than the perivascular pathway in what can and cannot permeate. This selectivity arises from the properties of the endothelial cells surrounding the microvessels. The brain is highly vascularized and cells within the parenchyma are usually within 20 µm of a microvessel [148]. Diffusion over distances this short is rapid. To reach the microvessel, substances must also cross the surrounding layer composed of glial endfeet. This is normally possible because the gaps between the endfeet are not sealed by tight junctions [149, 150]. Even the almost complete coverage of the endothelial cells by glial endfeet proposed by Mathiisen [149] leaves sufficient gaps (see Footnote 7). Thus normally it is the endothelial cells that are the site for the rate limiting steps in efflux across the blood–brain barrier. The current state of knowledge about the role of the endfeet was considered further in [4]."}

    2_test

    {"project":"2_test","denotations":[{"id":"30340614-20468051-30706066","span":{"begin":564,"end":567},"obj":"20468051"},{"id":"30340614-20468051-30706067","span":{"begin":674,"end":677},"obj":"20468051"},{"id":"30340614-27799072-30706068","span":{"begin":938,"end":939},"obj":"27799072"}],"text":"The blood–brain barrier is more selective than the perivascular pathway in what can and cannot permeate. This selectivity arises from the properties of the endothelial cells surrounding the microvessels. The brain is highly vascularized and cells within the parenchyma are usually within 20 µm of a microvessel [148]. Diffusion over distances this short is rapid. To reach the microvessel, substances must also cross the surrounding layer composed of glial endfeet. This is normally possible because the gaps between the endfeet are not sealed by tight junctions [149, 150]. Even the almost complete coverage of the endothelial cells by glial endfeet proposed by Mathiisen [149] leaves sufficient gaps (see Footnote 7). Thus normally it is the endothelial cells that are the site for the rate limiting steps in efflux across the blood–brain barrier. The current state of knowledge about the role of the endfeet was considered further in [4]."}