Hyaluronan degradation and release of a hyaluronan-aggrecan complex from perineuronal nets in the aged mouse brain

Perineuronal nets (PNNs) are insoluble aggregates of extracellular matrix molecules in the brain that consist of hyaluronan (HA) and chondroitin sulfate proteoglycans (CSPGs). PNNs promote the acquisition and storage of memories by stabilizing the formation of synapses in the adult brain. Although t...

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Published inBiochimica et biophysica acta. General subjects Vol. 1865; no. 2; p. 129804
Main Authors Sugitani, Kei, Egorova, Diana, Mizumoto, Shuji, Nishio, Shunsuke, Yamada, Shuhei, Kitagawa, Hiroshi, Oshima, Kenzi, Nadano, Daita, Matsuda, Tsukasa, Miyata, Shinji
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.02.2021
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Abstract Perineuronal nets (PNNs) are insoluble aggregates of extracellular matrix molecules in the brain that consist of hyaluronan (HA) and chondroitin sulfate proteoglycans (CSPGs). PNNs promote the acquisition and storage of memories by stabilizing the formation of synapses in the adult brain. Although the deterioration of PNNs has been suggested to contribute to the age-dependent decline in brain function, the molecular mechanisms underlying age-related changes in PNNs remain unclear. The amount and solubility of PNN components were investigated by sequential extraction followed by a disaccharide analysis and immunoblotting. We examined the interaction between HA and aggrecan, a major HA-binding CSPG, by combining mass spectrometry and pull-down assays. The solubility and amount of HA increased in the brain with age. Among several CSPGs, the solubility of aggrecan was selectively elevated during aging. In contrast to alternations in biochemical properties, the expression of PNN components at the transcript level was not markedly changed by aging. The increased solubility of aggrecan was not due to the loss of HA-binding properties. Our results indicated that the degradation of high-molecular-mass HA induced the release of the HA-aggrecan complex from PNNs in the aged brain. The present study revealed a novel mechanism underlying the age-related deterioration of PNNs in the brain. •Age-related changes in the biochemical properties of perineuronal nets (PNNs) in the mouse brain were investigated.•The solubility of hyaluronan (HA) and aggrecan increased in the mouse brain with age.•The increased solubility of aggrecan was not due to the loss of HA-binding properties.•Degradation of high-molecular-mass HA induced the release of the HA-aggrecan complex from PNNs in the aged brain.
AbstractList BACKGROUNDPerineuronal nets (PNNs) are insoluble aggregates of extracellular matrix molecules in the brain that consist of hyaluronan (HA) and chondroitin sulfate proteoglycans (CSPGs). PNNs promote the acquisition and storage of memories by stabilizing the formation of synapses in the adult brain. Although the deterioration of PNNs has been suggested to contribute to the age-dependent decline in brain function, the molecular mechanisms underlying age-related changes in PNNs remain unclear. METHODSThe amount and solubility of PNN components were investigated by sequential extraction followed by a disaccharide analysis and immunoblotting. We examined the interaction between HA and aggrecan, a major HA-binding CSPG, by combining mass spectrometry and pull-down assays. RESULTSThe solubility and amount of HA increased in the brain with age. Among several CSPGs, the solubility of aggrecan was selectively elevated during aging. In contrast to alternations in biochemical properties, the expression of PNN components at the transcript level was not markedly changed by aging. The increased solubility of aggrecan was not due to the loss of HA-binding properties. Our results indicated that the degradation of high-molecular-mass HA induced the release of the HA-aggrecan complex from PNNs in the aged brain. CONCLUSIONThe present study revealed a novel mechanism underlying the age-related deterioration of PNNs in the brain.
Perineuronal nets (PNNs) are insoluble aggregates of extracellular matrix molecules in the brain that consist of hyaluronan (HA) and chondroitin sulfate proteoglycans (CSPGs). PNNs promote the acquisition and storage of memories by stabilizing the formation of synapses in the adult brain. Although the deterioration of PNNs has been suggested to contribute to the age-dependent decline in brain function, the molecular mechanisms underlying age-related changes in PNNs remain unclear. The amount and solubility of PNN components were investigated by sequential extraction followed by a disaccharide analysis and immunoblotting. We examined the interaction between HA and aggrecan, a major HA-binding CSPG, by combining mass spectrometry and pull-down assays. The solubility and amount of HA increased in the brain with age. Among several CSPGs, the solubility of aggrecan was selectively elevated during aging. In contrast to alternations in biochemical properties, the expression of PNN components at the transcript level was not markedly changed by aging. The increased solubility of aggrecan was not due to the loss of HA-binding properties. Our results indicated that the degradation of high-molecular-mass HA induced the release of the HA-aggrecan complex from PNNs in the aged brain. The present study revealed a novel mechanism underlying the age-related deterioration of PNNs in the brain. •Age-related changes in the biochemical properties of perineuronal nets (PNNs) in the mouse brain were investigated.•The solubility of hyaluronan (HA) and aggrecan increased in the mouse brain with age.•The increased solubility of aggrecan was not due to the loss of HA-binding properties.•Degradation of high-molecular-mass HA induced the release of the HA-aggrecan complex from PNNs in the aged brain.
Perineuronal nets (PNNs) are insoluble aggregates of extracellular matrix molecules in the brain that consist of hyaluronan (HA) and chondroitin sulfate proteoglycans (CSPGs). PNNs promote the acquisition and storage of memories by stabilizing the formation of synapses in the adult brain. Although the deterioration of PNNs has been suggested to contribute to the age-dependent decline in brain function, the molecular mechanisms underlying age-related changes in PNNs remain unclear. The amount and solubility of PNN components were investigated by sequential extraction followed by a disaccharide analysis and immunoblotting. We examined the interaction between HA and aggrecan, a major HA-binding CSPG, by combining mass spectrometry and pull-down assays. The solubility and amount of HA increased in the brain with age. Among several CSPGs, the solubility of aggrecan was selectively elevated during aging. In contrast to alternations in biochemical properties, the expression of PNN components at the transcript level was not markedly changed by aging. The increased solubility of aggrecan was not due to the loss of HA-binding properties. Our results indicated that the degradation of high-molecular-mass HA induced the release of the HA-aggrecan complex from PNNs in the aged brain. The present study revealed a novel mechanism underlying the age-related deterioration of PNNs in the brain.
ArticleNumber 129804
Author Nishio, Shunsuke
Oshima, Kenzi
Miyata, Shinji
Mizumoto, Shuji
Sugitani, Kei
Egorova, Diana
Kitagawa, Hiroshi
Matsuda, Tsukasa
Nadano, Daita
Yamada, Shuhei
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  fullname: Egorova, Diana
  organization: Faculty of Agriculture, Tokyo University of Agriculture and Technology, 3-5-8 Saiwaicho, Fuchu, Tokyo 183-8509, Japan
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  givenname: Shuji
  surname: Mizumoto
  fullname: Mizumoto, Shuji
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  givenname: Shunsuke
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  givenname: Hiroshi
  surname: Kitagawa
  fullname: Kitagawa, Hiroshi
  organization: Laboratory of Biochemistry, Kobe Pharmaceutical University, 4-19-1 Motoyamakitamachi, Higashinada-Ku, Kobe 658-8558, Japan
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  givenname: Kenzi
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  fullname: Oshima, Kenzi
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– sequence: 8
  givenname: Daita
  surname: Nadano
  fullname: Nadano, Daita
  organization: Graduate School of Bioagricultural Sciences, Nagoya University, Furocho, Chikusa-Ku, Nagoya 464-8601, Japan
– sequence: 9
  givenname: Tsukasa
  surname: Matsuda
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  givenname: Shinji
  surname: Miyata
  fullname: Miyata, Shinji
  email: smiyata@go.tuat.ac.jp
  organization: Graduate School of Bioagricultural Sciences, Nagoya University, Furocho, Chikusa-Ku, Nagoya 464-8601, Japan
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Issue 2
Keywords Hyaluronan
Brain aging
Extracellular matrix
Chondroitin sulfate proteoglycan
Perineuronal net
Language English
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Snippet Perineuronal nets (PNNs) are insoluble aggregates of extracellular matrix molecules in the brain that consist of hyaluronan (HA) and chondroitin sulfate...
BACKGROUNDPerineuronal nets (PNNs) are insoluble aggregates of extracellular matrix molecules in the brain that consist of hyaluronan (HA) and chondroitin...
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StartPage 129804
SubjectTerms Aggrecans - metabolism
Aging
Animals
Brain - cytology
Brain - physiology
Brain aging
Chondroitin sulfate proteoglycan
Chondroitin Sulfate Proteoglycans - metabolism
Extracellular matrix
Extracellular Matrix - metabolism
Hyaluronan
Hyaluronic Acid - metabolism
Mice
Mice, Inbred C57BL
Mice, Inbred ICR
Neurons - cytology
Neurons - metabolism
Perineuronal net
Title Hyaluronan degradation and release of a hyaluronan-aggrecan complex from perineuronal nets in the aged mouse brain
URI https://dx.doi.org/10.1016/j.bbagen.2020.129804
https://www.ncbi.nlm.nih.gov/pubmed/33253804
https://search.proquest.com/docview/2466041907
Volume 1865
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