Neuroserpin: structure, function, physiology and pathology

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Neuroserpin: structure, function, physiology and pathology. / D'Acunto, Emanuela; Fra, Annamaria; Visentin, Cristina; Manno, Mauro; Ricagno, Stefano; Galliciotti, Giovanna; Miranda, Elena.

In: CELL MOL LIFE SCI, Vol. 78, No. 19-20, 10.2021, p. 6409-6430.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

Harvard

D'Acunto, E, Fra, A, Visentin, C, Manno, M, Ricagno, S, Galliciotti, G & Miranda, E 2021, 'Neuroserpin: structure, function, physiology and pathology', CELL MOL LIFE SCI, vol. 78, no. 19-20, pp. 6409-6430. https://doi.org/10.1007/s00018-021-03907-6

APA

D'Acunto, E., Fra, A., Visentin, C., Manno, M., Ricagno, S., Galliciotti, G., & Miranda, E. (2021). Neuroserpin: structure, function, physiology and pathology. CELL MOL LIFE SCI, 78(19-20), 6409-6430. https://doi.org/10.1007/s00018-021-03907-6

Vancouver

D'Acunto E, Fra A, Visentin C, Manno M, Ricagno S, Galliciotti G et al. Neuroserpin: structure, function, physiology and pathology. CELL MOL LIFE SCI. 2021 Oct;78(19-20):6409-6430. https://doi.org/10.1007/s00018-021-03907-6

Bibtex

@article{feda596e5e084e7c904898796bcac343,
title = "Neuroserpin: structure, function, physiology and pathology",
abstract = "Neuroserpin is a serine protease inhibitor identified in a search for proteins implicated in neuronal axon growth and synapse formation. Since its discovery over 30 years ago, it has been the focus of active research. Many efforts have concentrated in elucidating its neuroprotective role in brain ischemic lesions, the structural bases of neuroserpin conformational change and the effects of neuroserpin polymers that underlie the neurodegenerative disease FENIB (familial encephalopathy with neuroserpin inclusion bodies), but the investigation of the physiological roles of neuroserpin has increased over the last years. In this review, we present an updated and critical revision of the current literature dealing with neuroserpin, covering all aspects of research including the expression and physiological roles of neuroserpin, both inside and outside the nervous system; its inhibitory and non-inhibitory mechanisms of action; the molecular structure of the monomeric and polymeric conformations of neuroserpin, including a detailed description of the polymerisation mechanism; and the involvement of neuroserpin in human disease, with particular emphasis on FENIB. Finally, we briefly discuss the identification by genome-wide screening of novel neuroserpin variants and their possible pathogenicity.",
author = "Emanuela D'Acunto and Annamaria Fra and Cristina Visentin and Mauro Manno and Stefano Ricagno and Giovanna Galliciotti and Elena Miranda",
note = "{\textcopyright} 2021. The Author(s).",
year = "2021",
month = oct,
doi = "10.1007/s00018-021-03907-6",
language = "English",
volume = "78",
pages = "6409--6430",
journal = "CELL MOL LIFE SCI",
issn = "1420-682X",
publisher = "Birkhauser Verlag Basel",
number = "19-20",

}

RIS

TY - JOUR

T1 - Neuroserpin: structure, function, physiology and pathology

AU - D'Acunto, Emanuela

AU - Fra, Annamaria

AU - Visentin, Cristina

AU - Manno, Mauro

AU - Ricagno, Stefano

AU - Galliciotti, Giovanna

AU - Miranda, Elena

N1 - © 2021. The Author(s).

PY - 2021/10

Y1 - 2021/10

N2 - Neuroserpin is a serine protease inhibitor identified in a search for proteins implicated in neuronal axon growth and synapse formation. Since its discovery over 30 years ago, it has been the focus of active research. Many efforts have concentrated in elucidating its neuroprotective role in brain ischemic lesions, the structural bases of neuroserpin conformational change and the effects of neuroserpin polymers that underlie the neurodegenerative disease FENIB (familial encephalopathy with neuroserpin inclusion bodies), but the investigation of the physiological roles of neuroserpin has increased over the last years. In this review, we present an updated and critical revision of the current literature dealing with neuroserpin, covering all aspects of research including the expression and physiological roles of neuroserpin, both inside and outside the nervous system; its inhibitory and non-inhibitory mechanisms of action; the molecular structure of the monomeric and polymeric conformations of neuroserpin, including a detailed description of the polymerisation mechanism; and the involvement of neuroserpin in human disease, with particular emphasis on FENIB. Finally, we briefly discuss the identification by genome-wide screening of novel neuroserpin variants and their possible pathogenicity.

AB - Neuroserpin is a serine protease inhibitor identified in a search for proteins implicated in neuronal axon growth and synapse formation. Since its discovery over 30 years ago, it has been the focus of active research. Many efforts have concentrated in elucidating its neuroprotective role in brain ischemic lesions, the structural bases of neuroserpin conformational change and the effects of neuroserpin polymers that underlie the neurodegenerative disease FENIB (familial encephalopathy with neuroserpin inclusion bodies), but the investigation of the physiological roles of neuroserpin has increased over the last years. In this review, we present an updated and critical revision of the current literature dealing with neuroserpin, covering all aspects of research including the expression and physiological roles of neuroserpin, both inside and outside the nervous system; its inhibitory and non-inhibitory mechanisms of action; the molecular structure of the monomeric and polymeric conformations of neuroserpin, including a detailed description of the polymerisation mechanism; and the involvement of neuroserpin in human disease, with particular emphasis on FENIB. Finally, we briefly discuss the identification by genome-wide screening of novel neuroserpin variants and their possible pathogenicity.

U2 - 10.1007/s00018-021-03907-6

DO - 10.1007/s00018-021-03907-6

M3 - SCORING: Review article

C2 - 34405255

VL - 78

SP - 6409

EP - 6430

JO - CELL MOL LIFE SCI

JF - CELL MOL LIFE SCI

SN - 1420-682X

IS - 19-20

ER -