Excessive expression of progranulin leads to neurotoxicity rather than neuroprotection

Frontotemporal dementia (FTD) is an early onset form of dementia characterized by frontotemporal lobar atrophy accompanied by behavioral, personality, language, and motor deficits. Heterozygous mutations in GRN gene encoding progranulin (PGRN) are the genetic causes of FTD. Since PGRN is a neurotrop...

Full description

Saved in:
Bibliographic Details
Main Authors: Shinya Kusakari, Hiroaki Suzuki, Mikiro Nawa, Katsuko Sudo, Rio Yamazaki, Tamami Miyagi, Tomoko Ohara, Masaaki Matsuoka, Kohsuke Kanekura
Format: Article
Language:English
Published: Elsevier 2025-06-01
Series:Neurobiology of Disease
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996125001111
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850179789583810560
author Shinya Kusakari
Hiroaki Suzuki
Mikiro Nawa
Katsuko Sudo
Rio Yamazaki
Tamami Miyagi
Tomoko Ohara
Masaaki Matsuoka
Kohsuke Kanekura
author_facet Shinya Kusakari
Hiroaki Suzuki
Mikiro Nawa
Katsuko Sudo
Rio Yamazaki
Tamami Miyagi
Tomoko Ohara
Masaaki Matsuoka
Kohsuke Kanekura
author_sort Shinya Kusakari
collection DOAJ
description Frontotemporal dementia (FTD) is an early onset form of dementia characterized by frontotemporal lobar atrophy accompanied by behavioral, personality, language, and motor deficits. Heterozygous mutations in GRN gene encoding progranulin (PGRN) are the genetic causes of FTD. Since PGRN is a neurotrophic and anti-inflammatory factor, most FTD-related PGRN mutations are thought to cause FTD due to haploinsufficiency. Therefore, therapies that increase PGRN levels by the administration of recombinant PGRN or viral vectors are attracting attention as an approach to the treatment of FTD. However, the mechanisms underlying the neuroprotective effects of PGRN remain unclear. To investigate the neuroprotective mechanisms of PGRN in vivo, we generated human PGRN transgenic (Tg) mice using the CAG promoter. Unexpectedly, mice overexpressing wild-type human PGRN showed a shortened lifespan and cerebellar dysfunction, including the loss of Purkinje cells. Furthermore, PGRN Tg mice developed cognitive impairment, gliosis, and lysosomal abnormalities. FTD-causative R432C-PGRN mutant Tg mice also showed FTD-like phenotypes, such as neuronal loss, gliosis, and behavioral deficits. In cultured cells, overexpression of PGRN induced endoplasmic reticulum (ER) stress and apoptotic cell death, suggesting that continuous increases in PGRN expression through viral vectors or genetic manipulation are neurotoxic and that PGRN-replacement therapy may be required to maintain optimal PGRN levels for each neuron type and brain region.
format Article
id doaj-art-ba8a79a0e6354a1e83d7250d208aa7af
institution OA Journals
issn 1095-953X
language English
publishDate 2025-06-01
publisher Elsevier
record_format Article
series Neurobiology of Disease
spelling doaj-art-ba8a79a0e6354a1e83d7250d208aa7af2025-08-20T02:18:24ZengElsevierNeurobiology of Disease1095-953X2025-06-0120910689510.1016/j.nbd.2025.106895Excessive expression of progranulin leads to neurotoxicity rather than neuroprotectionShinya Kusakari0Hiroaki Suzuki1Mikiro Nawa2Katsuko Sudo3Rio Yamazaki4Tamami Miyagi5Tomoko Ohara6Masaaki Matsuoka7Kohsuke Kanekura8Department of Pharmacology, Tokyo Medical University, Shinjuku-ku, Tokyo, Japan; Corresponding authors.Department of Pharmacology, Tokyo Medical University, Shinjuku-ku, Tokyo, JapanDepartment of Pharmacology, Tokyo Medical University, Shinjuku-ku, Tokyo, JapanPre-Clinical Research Center, Tokyo Medical University, Shinjuku-ku, Tokyo, JapanDepartment of Pharmacology, Tokyo Medical University, Shinjuku-ku, Tokyo, JapanDepartment of Pharmacology, Tokyo Medical University, Shinjuku-ku, Tokyo, JapanDepartment of Pharmacology, Tokyo Medical University, Shinjuku-ku, Tokyo, JapanDepartment of Pharmacology, Tokyo Medical University, Shinjuku-ku, Tokyo, JapanDepartment of Pharmacology, Tokyo Medical University, Shinjuku-ku, Tokyo, Japan; Corresponding authors.Frontotemporal dementia (FTD) is an early onset form of dementia characterized by frontotemporal lobar atrophy accompanied by behavioral, personality, language, and motor deficits. Heterozygous mutations in GRN gene encoding progranulin (PGRN) are the genetic causes of FTD. Since PGRN is a neurotrophic and anti-inflammatory factor, most FTD-related PGRN mutations are thought to cause FTD due to haploinsufficiency. Therefore, therapies that increase PGRN levels by the administration of recombinant PGRN or viral vectors are attracting attention as an approach to the treatment of FTD. However, the mechanisms underlying the neuroprotective effects of PGRN remain unclear. To investigate the neuroprotective mechanisms of PGRN in vivo, we generated human PGRN transgenic (Tg) mice using the CAG promoter. Unexpectedly, mice overexpressing wild-type human PGRN showed a shortened lifespan and cerebellar dysfunction, including the loss of Purkinje cells. Furthermore, PGRN Tg mice developed cognitive impairment, gliosis, and lysosomal abnormalities. FTD-causative R432C-PGRN mutant Tg mice also showed FTD-like phenotypes, such as neuronal loss, gliosis, and behavioral deficits. In cultured cells, overexpression of PGRN induced endoplasmic reticulum (ER) stress and apoptotic cell death, suggesting that continuous increases in PGRN expression through viral vectors or genetic manipulation are neurotoxic and that PGRN-replacement therapy may be required to maintain optimal PGRN levels for each neuron type and brain region.http://www.sciencedirect.com/science/article/pii/S0969996125001111Progranulin (PGRN)Frontotemporal dementiaNeurodegenerationNeuronal death
spellingShingle Shinya Kusakari
Hiroaki Suzuki
Mikiro Nawa
Katsuko Sudo
Rio Yamazaki
Tamami Miyagi
Tomoko Ohara
Masaaki Matsuoka
Kohsuke Kanekura
Excessive expression of progranulin leads to neurotoxicity rather than neuroprotection
Neurobiology of Disease
Progranulin (PGRN)
Frontotemporal dementia
Neurodegeneration
Neuronal death
title Excessive expression of progranulin leads to neurotoxicity rather than neuroprotection
title_full Excessive expression of progranulin leads to neurotoxicity rather than neuroprotection
title_fullStr Excessive expression of progranulin leads to neurotoxicity rather than neuroprotection
title_full_unstemmed Excessive expression of progranulin leads to neurotoxicity rather than neuroprotection
title_short Excessive expression of progranulin leads to neurotoxicity rather than neuroprotection
title_sort excessive expression of progranulin leads to neurotoxicity rather than neuroprotection
topic Progranulin (PGRN)
Frontotemporal dementia
Neurodegeneration
Neuronal death
url http://www.sciencedirect.com/science/article/pii/S0969996125001111
work_keys_str_mv AT shinyakusakari excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection
AT hiroakisuzuki excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection
AT mikironawa excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection
AT katsukosudo excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection
AT rioyamazaki excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection
AT tamamimiyagi excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection
AT tomokoohara excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection
AT masaakimatsuoka excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection
AT kohsukekanekura excessiveexpressionofprogranulinleadstoneurotoxicityratherthanneuroprotection