Clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells.

Neuronal differentiation from expanded human ventral mesencephalic neural precursor cells (NPCs) is very limited. Astrocytes are known to secrete neurotrophic factors, and so in order to enhance neuronal survival from NPCs, we tested the effect of regional astrocyte-conditioned medium (ACM) from the...

Full description

Bibliographic Details
Main Authors: Cordero-Llana, O, Scott, SA, Maslen, S, Anderson, J, Boyle, J, Chowhdury, R, Tyers, P, Barker, R, Kelly, C, Rosser, A, Stephens, E, Chandran, S, Caldwell, M
Format: Journal article
Language:English
Published: 2011
_version_ 1797083237150883840
author Cordero-Llana, O
Scott, SA
Maslen, S
Anderson, J
Boyle, J
Chowhdury, R
Tyers, P
Barker, R
Kelly, C
Rosser, A
Stephens, E
Chandran, S
Caldwell, M
author_facet Cordero-Llana, O
Scott, SA
Maslen, S
Anderson, J
Boyle, J
Chowhdury, R
Tyers, P
Barker, R
Kelly, C
Rosser, A
Stephens, E
Chandran, S
Caldwell, M
author_sort Cordero-Llana, O
collection OXFORD
description Neuronal differentiation from expanded human ventral mesencephalic neural precursor cells (NPCs) is very limited. Astrocytes are known to secrete neurotrophic factors, and so in order to enhance neuronal survival from NPCs, we tested the effect of regional astrocyte-conditioned medium (ACM) from the rat cortex, hippocampus and midbrain on this process. Human NPC's were expanded in FGF-2 before differentiation for 1 or 4 weeks in ACM. The results show that ACM from the hippocampus and midbrain increase the number of neurons from expanded human NPCs, an effect that was not observed with cortical ACM. In addition, both hippocampal and midbrain ACM increased the number and length of phosphorylated neurofilaments. MALDI-TOF analysis used to determine differences in media revealed that although all three regional ACMs had cystatin C, α-2 macroglobulin, extracellular matrix glycoprotein and vimentin, only hippocampal and midbrain ACM also contained clusterin, which when immunodepleted from midbrain ACM eliminated the observed effects on neuronal differentiation. Furthermore, clusterin is a highly glycosylated protein that has no effect on cell proliferation but decreases apoptotic nuclei and causes a sustained increase in phosphorylated extracellular signal-regulated kinase, implicating its role in cell survival and differentiation. These findings further reveal differential effects of regional astrocytes on NPC behavior and identify clusterin as an important mediator of NPC-derived neuronal survival and differentiation.
first_indexed 2024-03-07T01:38:52Z
format Journal article
id oxford-uuid:96241b01-0617-441e-9e51-68ee3bc6f499
institution University of Oxford
language English
last_indexed 2024-03-07T01:38:52Z
publishDate 2011
record_format dspace
spelling oxford-uuid:96241b01-0617-441e-9e51-68ee3bc6f4992022-03-26T23:51:04ZClusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:96241b01-0617-441e-9e51-68ee3bc6f499EnglishSymplectic Elements at Oxford2011Cordero-Llana, OScott, SAMaslen, SAnderson, JBoyle, JChowhdury, RTyers, PBarker, RKelly, CRosser, AStephens, EChandran, SCaldwell, MNeuronal differentiation from expanded human ventral mesencephalic neural precursor cells (NPCs) is very limited. Astrocytes are known to secrete neurotrophic factors, and so in order to enhance neuronal survival from NPCs, we tested the effect of regional astrocyte-conditioned medium (ACM) from the rat cortex, hippocampus and midbrain on this process. Human NPC's were expanded in FGF-2 before differentiation for 1 or 4 weeks in ACM. The results show that ACM from the hippocampus and midbrain increase the number of neurons from expanded human NPCs, an effect that was not observed with cortical ACM. In addition, both hippocampal and midbrain ACM increased the number and length of phosphorylated neurofilaments. MALDI-TOF analysis used to determine differences in media revealed that although all three regional ACMs had cystatin C, α-2 macroglobulin, extracellular matrix glycoprotein and vimentin, only hippocampal and midbrain ACM also contained clusterin, which when immunodepleted from midbrain ACM eliminated the observed effects on neuronal differentiation. Furthermore, clusterin is a highly glycosylated protein that has no effect on cell proliferation but decreases apoptotic nuclei and causes a sustained increase in phosphorylated extracellular signal-regulated kinase, implicating its role in cell survival and differentiation. These findings further reveal differential effects of regional astrocytes on NPC behavior and identify clusterin as an important mediator of NPC-derived neuronal survival and differentiation.
spellingShingle Cordero-Llana, O
Scott, SA
Maslen, S
Anderson, J
Boyle, J
Chowhdury, R
Tyers, P
Barker, R
Kelly, C
Rosser, A
Stephens, E
Chandran, S
Caldwell, M
Clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells.
title Clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells.
title_full Clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells.
title_fullStr Clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells.
title_full_unstemmed Clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells.
title_short Clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells.
title_sort clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cells
work_keys_str_mv AT corderollanao clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT scottsa clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT maslens clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT andersonj clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT boylej clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT chowhduryr clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT tyersp clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT barkerr clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT kellyc clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT rossera clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT stephense clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT chandrans clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells
AT caldwellm clusterinsecretedbyastrocytesenhancesneuronaldifferentiationfromhumanneuralprecursorcells