A Narrative Review of the Role of Transthyretin in Health and Disease
Transthyretin (TTR) is a tetrameric transport protein highly conserved through vertebrate evolution and synthesized in the liver, choroid plexus, and retinal pigment epithelium. TTR transports the thyroid hormone thyroxine and the retinol-binding protein (RBP) bound to retinol (vitamin A). Mutations...
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Published in | Neurology and therapy Vol. 9; no. 2; pp. 395 - 402 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Springer Healthcare
01.12.2020
Adis, Springer Healthcare |
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Abstract | Transthyretin (TTR) is a tetrameric transport protein highly conserved through vertebrate evolution and synthesized in the liver, choroid plexus, and retinal pigment epithelium. TTR transports the thyroid hormone thyroxine and the retinol-binding protein (RBP) bound to retinol (vitamin A). Mutations in TTR are associated with inherited transthyretin amyloidosis (ATTRv), a progressive, debilitating disease that is ultimately fatal and is characterized by misfolding of TTR and aggregation as amyloid fibrils, predominantly leading to cardiomyopathy or polyneuropathy depending on the particular TTR mutation. Transthyretin amyloid cardiomyopathy can also occur as an age-related disease caused by misfolding of wild-type TTR. Apart from its transport role, little is known about possible additional physiological functions of TTR. Evidence from animal model systems in which TTR has been disrupted via gene knockout is adding to our cumulative understanding of TTR function. There is growing evidence that TTR may have a role in neuroprotection and promotion of neurite outgrowth in response to injury. Here, we review the literature describing potential roles of TTR in neurobiology and in the pathophysiology of diseases other than ATTR amyloidosis. A greater understanding of these processes may also contribute to further clarification of the pathology of ATTR and the effects of potential therapies for TTR-related conditions. |
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AbstractList | Transthyretin (TTR) is a tetrameric transport protein highly conserved through vertebrate evolution and synthesized in the liver, choroid plexus, and retinal pigment epithelium. TTR transports the thyroid hormone thyroxine and the retinol-binding protein (RBP) bound to retinol (vitamin A). Mutations in TTR are associated with inherited transthyretin amyloidosis (ATTRv), a progressive, debilitating disease that is ultimately fatal and is characterized by misfolding of TTR and aggregation as amyloid fibrils, predominantly leading to cardiomyopathy or polyneuropathy depending on the particular TTR mutation. Transthyretin amyloid cardiomyopathy can also occur as an age-related disease caused by misfolding of wild-type TTR. Apart from its transport role, little is known about possible additional physiological functions of TTR. Evidence from animal model systems in which TTR has been disrupted via gene knockout is adding to our cumulative understanding of TTR function. There is growing evidence that TTR may have a role in neuroprotection and promotion of neurite outgrowth in response to injury. Here, we review the literature describing potential roles of TTR in neurobiology and in the pathophysiology of diseases other than ATTR amyloidosis. A greater understanding of these processes may also contribute to further clarification of the pathology of ATTR and the effects of potential therapies for TTR-related conditions. Abstract Transthyretin (TTR) is a tetrameric transport protein highly conserved through vertebrate evolution and synthesized in the liver, choroid plexus, and retinal pigment epithelium. TTR transports the thyroid hormone thyroxine and the retinol-binding protein (RBP) bound to retinol (vitamin A). Mutations in TTR are associated with inherited transthyretin amyloidosis (ATTRv), a progressive, debilitating disease that is ultimately fatal and is characterized by misfolding of TTR and aggregation as amyloid fibrils, predominantly leading to cardiomyopathy or polyneuropathy depending on the particular TTR mutation. Transthyretin amyloid cardiomyopathy can also occur as an age-related disease caused by misfolding of wild-type TTR. Apart from its transport role, little is known about possible additional physiological functions of TTR. Evidence from animal model systems in which TTR has been disrupted via gene knockout is adding to our cumulative understanding of TTR function. There is growing evidence that TTR may have a role in neuroprotection and promotion of neurite outgrowth in response to injury. Here, we review the literature describing potential roles of TTR in neurobiology and in the pathophysiology of diseases other than ATTR amyloidosis. A greater understanding of these processes may also contribute to further clarification of the pathology of ATTR and the effects of potential therapies for TTR-related conditions. |
Author | Liz, Marcia Almeida Mallaina, Pablo Fernandez-Arias, Maria Isabel Obici, Laura Coelho, Teresa Bellotti, Vittorio |
Author_xml | – sequence: 1 givenname: Marcia Almeida surname: Liz fullname: Liz, Marcia Almeida organization: Instituto de Investigação e Inovação em Saúde (i3S), Universidade Do Porto – sequence: 2 givenname: Teresa surname: Coelho fullname: Coelho, Teresa organization: Centro Hospitalar Universitário Do Porto – sequence: 3 givenname: Vittorio surname: Bellotti fullname: Bellotti, Vittorio organization: Wolfson Drug Discovery Unit, Division of Medicine, Centre for Amyloidosis and Acute Phase Proteins, University College London, Department of Molecular Medicine, Institute of Biochemistry, University of Pavia – sequence: 4 givenname: Maria Isabel surname: Fernandez-Arias fullname: Fernandez-Arias, Maria Isabel organization: Pfizer Global Medical Affairs – sequence: 5 givenname: Pablo surname: Mallaina fullname: Mallaina, Pablo organization: Pfizer Global Medical Affairs – sequence: 6 givenname: Laura orcidid: 0000-0001-7468-700X surname: Obici fullname: Obici, Laura email: l.obici@smatteo.pv.it organization: Amyloidosis Research and Treatment Centre, IRCCS Fondazione Policlinico San Matteo |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33001386$$D View this record in MEDLINE/PubMed |
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Keywords | Neuroprotection Amyloidosis Alzheimer’s disease Neurodegeneration Transthyretin |
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Snippet | Transthyretin (TTR) is a tetrameric transport protein highly conserved through vertebrate evolution and synthesized in the liver, choroid plexus, and retinal... Abstract Transthyretin (TTR) is a tetrameric transport protein highly conserved through vertebrate evolution and synthesized in the liver, choroid plexus, and... |
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SubjectTerms | Alzheimer’s disease Amyloidosis Internal Medicine Medicine Medicine & Public Health Neurodegeneration Neurology Neuroprotection Review Transthyretin |
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Title | A Narrative Review of the Role of Transthyretin in Health and Disease |
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