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The Effect of Hapln4 Link Protein Deficiency on Extracellular Space Diffusion Parameters and Perineuronal Nets in the Auditory System During Aging
P. Sucha, M. Chmelova, M. Kamenicka, M. Bochin, T. Oohashi, L. Vargova,
Language English Country United States
Document type Journal Article
Grant support
16-10214S
Grantová Agentura České Republiky
19H04754
Grant-in-Aid for Scientific Research on Innovative Areas
NLK
ProQuest Central
from 1997-01-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2009-08-01 to 1 year ago
Health & Medicine (ProQuest)
from 1997-01-01 to 1 year ago
- MeSH
- Trapezoid Body metabolism pathology MeSH
- Diffusion * MeSH
- Extracellular Matrix Proteins deficiency MeSH
- Extracellular Matrix metabolism pathology MeSH
- Extracellular Space metabolism MeSH
- Mice, Inbred C57BL MeSH
- Mice, Knockout MeSH
- Mice MeSH
- Protein Deficiency metabolism pathology MeSH
- Organ Culture Techniques MeSH
- Peripheral Nerves metabolism pathology MeSH
- Nerve Tissue Proteins deficiency MeSH
- Auditory Pathways metabolism pathology MeSH
- Aging metabolism pathology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Hapln4 is a link protein which stabilizes the binding between lecticans and hyaluronan in perineuronal nets (PNNs) in specific brain regions, including the medial nucleus of the trapezoid body (MNTB). The aim of this study was: (1) to reveal possible age-related alterations in the extracellular matrix composition in the MNTB and inferior colliculus, which was devoid of Hapln4 and served as a negative control, (2) to determine the impact of the Hapln4 deletion on the values of the ECS diffusion parameters in young and aged animals and (3) to verify that PNNs moderate age-related changes in the ECS diffusion, and that Hapln4-brevican complex is indispensable for the correct protective function of the PNNs. To achieve this, we evaluated the ECS diffusion parameters using the real-time iontophoretic method in the selected region in young adult (3 to 6-months-old) and aged (12 to 18-months-old) wild type and Hapln4 knock-out (KO) mice. The results were correlated with an immunohistochemical analysis of the ECM composition and astrocyte morphology. We report that the ECM composition is altered in the aged MNTB and aging is a critical point, revealing the effect of Hapln4 deficiency on the ECS diffusion. All of our findings support the hypothesis that the ECM changes in the MNTB of aged KO animals affect the ECS parameters indirectly, via morphological changes of astrocytes, which are in direct contact with synapses and can be influenced by the ongoing synaptic transmission altered by shifts in the ECM composition.
References provided by Crossref.org
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- $a Sucha, Petra $u Department of Neuroscience, 2nd Faculty of Medicine, Charles University, V Úvalu 84, 150 06, Prague 5, Czech Republic. Department of Cellular Neurophysiology, Institute of Experimental Medicine AS CR, v.v.i., Prague, Czech Republic.
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