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 inNeurology and therapy Vol. 9; no. 2; pp. 395 - 402
Main Authors Liz, Marcia Almeida, Coelho, Teresa, Bellotti, Vittorio, Fernandez-Arias, Maria Isabel, Mallaina, Pablo, Obici, Laura
Format Journal Article
LanguageEnglish
Published Cheshire 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.
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
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  givenname: Teresa
  surname: Coelho
  fullname: Coelho, Teresa
  organization: Centro Hospitalar Universitário Do Porto
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  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
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  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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Issue 2
Keywords Neuroprotection
Amyloidosis
Alzheimer’s disease
Neurodegeneration
Transthyretin
Language English
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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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StartPage 395
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
URI https://link.springer.com/article/10.1007/s40120-020-00217-0
https://www.ncbi.nlm.nih.gov/pubmed/33001386
https://search.proquest.com/docview/2447841096
https://pubmed.ncbi.nlm.nih.gov/PMC7606379
https://doaj.org/article/cdd2e67efd9647afba76d20bca39ddb0
Volume 9
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