Decreased Expression of Glial-Derived Neurotrophic Factor Receptors in Glaucomatous Human Retinas

The purpose of this study was to examine the expression of glial-derived neurotrophic factor (GDNF), the GDNF receptors GFRα1 and GFRα2, ciliary neurotrophic factor (CNTF), and the CNTF receptor CNTFRα in normal and glaucomatous human tissue. Human retinas were collected from 8 donors that had been...

Full description

Saved in:
Bibliographic Details
Published inCurrent eye research Vol. 47; no. 4; pp. 597 - 605
Main Authors Akurathi, Abhigna, Boese, Erin A., Kardon, Randy H., Ledolter, Johannes, Kuehn, Markus H., Harper, Matthew M.
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 03.04.2022
Subjects
Online AccessGet full text

Cover

Loading…
Abstract The purpose of this study was to examine the expression of glial-derived neurotrophic factor (GDNF), the GDNF receptors GFRα1 and GFRα2, ciliary neurotrophic factor (CNTF), and the CNTF receptor CNTFRα in normal and glaucomatous human tissue. Human retinas were collected from 8 donors that had been clinically diagnosed and treated for glaucoma, and also from 9 healthy control donors. Immunohistochemical analysis for each trophic factor and receptor was performed. The percent of each retinal section labeled with each antibody was quantified for the total retinal thickness, and separately for the retinal ganglion cell (RGC) complex + retinal nerve fiber layer (RNFL). The expression of each protein was correlated with measures of the subject's ocular histories. The percentage area immunopositive for GFRα2 was significantly decreased in the total retinal thickness containing all retinal layers and in the combined RGC complex + RNFL in glaucomatous eyes in both the peripapillary region and more peripheral retinal locations. We also observed a decrease in GFRα1 expression in the peripapillary RGC Complex + RNFL in glaucoma patients compared to healthy control patients. We also observed a relationship between GDNF and its receptors with several outcomes obtained from the medical record. No differences in CNTF or CNTFR labeling were observed. Decreases in GDNF receptor expression in glaucomatous tissue may limit the potential for neuroprotective therapy by supplementation with GDNF.
AbstractList The purpose of this study was to examine the expression of glial-derived neurotrophic factor (GDNF), the GDNF receptors GFRα1 and GFRα2, ciliary neurotrophic factor (CNTF), and the CNTF receptor CNTFRα in normal and glaucomatous human tissue. Human retinas were collected from 8 donors that had been clinically diagnosed and treated for glaucoma, and also from 9 healthy control donors. Immunohistochemical analysis for each trophic factor and receptor was performed. The percent of each retinal section labeled with each antibody was quantified for the total retinal thickness, and separately for the retinal ganglion cell (RGC) complex + retinal nerve fiber layer (RNFL). The expression of each protein was correlated with measures of the subject's ocular histories. The percentage area immunopositive for GFRα2 was significantly decreased in the total retinal thickness containing all retinal layers and in the combined RGC complex + RNFL in glaucomatous eyes in both the peripapillary region and more peripheral retinal locations. We also observed a decrease in GFRα1 expression in the peripapillary RGC Complex + RNFL in glaucoma patients compared to healthy control patients. We also observed a relationship between GDNF and its receptors with several outcomes obtained from the medical record. No differences in CNTF or CNTFR labeling were observed. Decreases in GDNF receptor expression in glaucomatous tissue may limit the potential for neuroprotective therapy by supplementation with GDNF.
The purpose of this study was to examine the expression of glial-derived neurotrophic factor (GDNF), the GDNF receptors GFRα1 and GFRα2, ciliary neurotrophic factor (CNTF), and the CNTF receptor CNTFRα in normal and glaucomatous human tissue.PURPOSEThe purpose of this study was to examine the expression of glial-derived neurotrophic factor (GDNF), the GDNF receptors GFRα1 and GFRα2, ciliary neurotrophic factor (CNTF), and the CNTF receptor CNTFRα in normal and glaucomatous human tissue.Human retinas were collected from 8 donors that had been clinically diagnosed and treated for glaucoma, and also from 9 healthy control donors. Immunohistochemical analysis for each trophic factor and receptor was performed. The percent of each retinal section labeled with each antibody was quantified for the total retinal thickness, and separately for the retinal ganglion cell (RGC) complex + retinal nerve fiber layer (RNFL). The expression of each protein was correlated with measures of the subject's ocular histories.METHODSHuman retinas were collected from 8 donors that had been clinically diagnosed and treated for glaucoma, and also from 9 healthy control donors. Immunohistochemical analysis for each trophic factor and receptor was performed. The percent of each retinal section labeled with each antibody was quantified for the total retinal thickness, and separately for the retinal ganglion cell (RGC) complex + retinal nerve fiber layer (RNFL). The expression of each protein was correlated with measures of the subject's ocular histories.The percentage area immunopositive for GFRα2 was significantly decreased in the total retinal thickness containing all retinal layers and in the combined RGC complex + RNFL in glaucomatous eyes in both the peripapillary region and more peripheral retinal locations. We also observed a decrease in GFRα1 expression in the peripapillary RGC Complex + RNFL in glaucoma patients compared to healthy control patients. We also observed a relationship between GDNF and its receptors with several outcomes obtained from the medical record. No differences in CNTF or CNTFR labeling were observed.RESULTSThe percentage area immunopositive for GFRα2 was significantly decreased in the total retinal thickness containing all retinal layers and in the combined RGC complex + RNFL in glaucomatous eyes in both the peripapillary region and more peripheral retinal locations. We also observed a decrease in GFRα1 expression in the peripapillary RGC Complex + RNFL in glaucoma patients compared to healthy control patients. We also observed a relationship between GDNF and its receptors with several outcomes obtained from the medical record. No differences in CNTF or CNTFR labeling were observed.Decreases in GDNF receptor expression in glaucomatous tissue may limit the potential for neuroprotective therapy by supplementation with GDNF.CONCLUSIONDecreases in GDNF receptor expression in glaucomatous tissue may limit the potential for neuroprotective therapy by supplementation with GDNF.
Author Ledolter, Johannes
Kardon, Randy H.
Kuehn, Markus H.
Akurathi, Abhigna
Harper, Matthew M.
Boese, Erin A.
Author_xml – sequence: 1
  givenname: Abhigna
  surname: Akurathi
  fullname: Akurathi, Abhigna
  organization: Department of Biomedical Engineering, University of Iowa
– sequence: 2
  givenname: Erin A.
  surname: Boese
  fullname: Boese, Erin A.
  organization: Departmentsof Ophthalmology and Visual Sciences, University of Iowa
– sequence: 3
  givenname: Randy H.
  surname: Kardon
  fullname: Kardon, Randy H.
  organization: Veterans Administration Center for the Prevention and Treatment of Visual Loss, VA Medical Center
– sequence: 4
  givenname: Johannes
  surname: Ledolter
  fullname: Ledolter, Johannes
  organization: The University of Iowa Tippie College of Business
– sequence: 5
  givenname: Markus H.
  surname: Kuehn
  fullname: Kuehn, Markus H.
  organization: Veterans Administration Center for the Prevention and Treatment of Visual Loss, VA Medical Center
– sequence: 6
  givenname: Matthew M.
  surname: Harper
  fullname: Harper, Matthew M.
  organization: Department of Biology, The University of Iowa
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34738835$$D View this record in MEDLINE/PubMed
BookMark eNqFkE1v1DAQhi1URLfb_oSiHLmkTOzEScQF1E-kCiTUuzXxjlWjxA62U-i_x9FuOXCAi23NPO_I85ywI-cdMXZewUUFHbwH3lZCduKCA6_yAbyH9hXbVLWEkufiEdusTLlCx-wkxu8Aa6F-w45F3YquE82G4RXpQBhpV1z_mgPFaL0rvCluR4tjeUXBPuXeF1qCT8HPj1YXN6iTD8U30jTnRyysyzgu2k-Y_BKLu2VCl_vJOoyn7LXBMdLZ4d6yh5vrh8u78v7r7efLT_elFlKmUkLfVqY3XU_CIAkN9QAVEEppUNIw6FoPDXZa5o4E3tWDRqjzFsPAm53Ysnf7sXPwPxaKSU02ahpHdJT_pHjT17xv27z5lr09oMsw0U7NwU4YntWLlQw0e0AHH2Mg8wepQK321Yt9tdpXB_s59-GvnLYJUzaaAtrxv-mP-7R1xocJf_ow7lTC59EHE9BpG5X494jf5eydvA
CitedBy_id crossref_primary_10_1007_s10571_022_01280_x
crossref_primary_10_1089_jop_2024_0041
crossref_primary_10_1101_cshperspect_a041665
Cites_doi 10.1080/08977190410001715181
10.1016/j.exer.2018.09.006
10.1136/bjo.80.5.389
10.1038/nrn812
10.3390/cells9092082
10.2337/diacare.25.6.1060
10.1016/S0002-9394(98)00223-2
10.1038/nrn2054
10.1016/j.preteyeres.2011.11.005
10.1111/j.0953-816X.2003.03107.x
10.3390/ph14010050
10.1167/iovs.14-15266
10.1006/exer.2001.1145
10.1167/iovs.08-3013
ContentType Journal Article
Copyright 2022 Taylor & Francis Group, LLC 2022
Copyright_xml – notice: 2022 Taylor & Francis Group, LLC 2022
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1080/02713683.2021.2002907
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Anatomy & Physiology
EISSN 1460-2202
EndPage 605
ExternalDocumentID 34738835
10_1080_02713683_2021_2002907
2002907
Genre Research Article
Research Support, U.S. Gov't, Non-P.H.S
Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: NEI NIH HHS
  grantid: R01 EY034534
– fundername: RRD VA
  grantid: I01 RX002860
– fundername: RRD VA
  grantid: I50 RX003002
GroupedDBID ---
00X
03L
0BK
0R~
29F
36B
4.4
5GY
5RE
AALUX
AAMIU
AAPUL
AAQRR
ABBKH
ABDBF
ABEIZ
ABJNI
ABLIJ
ABLJU
ABLKL
ABUPF
ABXYU
ACENM
ACGEJ
ACGFS
ACIEZ
ACNCT
ACUHS
ADCVX
ADRBQ
ADXPE
AECIN
AENEX
AEOZL
AFKVX
AGDLA
AGFJD
AGRBW
AGYJP
AIJEM
AIRBT
AJWEG
AKBVH
ALMA_UNASSIGNED_HOLDINGS
ALQZU
ALYBC
AMDAE
BABNJ
BLEHA
BOHLJ
CCCUG
CS3
DKSSO
DU5
EAP
EBC
EBD
EBS
EMB
EMK
EMOBN
EPL
ESX
F5P
H13
HZ~
KRBQP
KSSTO
KWAYT
KYCEM
LJTGL
M4Z
O9-
P2P
PQQKQ
RNANH
RVRKI
SV3
TBQAZ
TDBHL
TERGH
TFDNU
TFL
TFW
TUROJ
TUS
UEQFS
V1S
~1N
AAGDL
AAYXX
ABWVI
ADYSH
AFRVT
AMPGV
CITATION
.55
.GJ
34G
39C
53G
5VS
AALIY
AAORF
AAPXX
ABWCV
ABZEW
ACKZS
ACOPL
ADFOM
ADFZZ
AEIIZ
AFFNX
AFLEI
AJVHN
AWYRJ
BRMBE
CAG
CGR
COF
CUY
CVF
CYYVM
CZDIS
DRXRE
DWTOO
ECM
EIF
EJD
JENTW
M44
NPM
NUSFT
QQXMO
RIG
X7M
ZGI
ZXP
7X8
ID FETCH-LOGICAL-c366t-60971f9f89e3fae3c04b010ea66fa6ebbc4cb5a8c6c0460284bca04883bb25d3
ISSN 0271-3683
1460-2202
IngestDate Fri Jul 11 02:51:21 EDT 2025
Thu Apr 03 07:09:16 EDT 2025
Tue Jul 01 00:42:49 EDT 2025
Thu Apr 24 23:05:51 EDT 2025
Wed Dec 25 09:06:28 EST 2024
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords CNTF
GDNF
glaucoma
neuroprotection
neurotrophic growth factor
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c366t-60971f9f89e3fae3c04b010ea66fa6ebbc4cb5a8c6c0460284bca04883bb25d3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 34738835
PQID 2594297747
PQPubID 23479
PageCount 9
ParticipantIDs informaworld_taylorfrancis_310_1080_02713683_2021_2002907
crossref_citationtrail_10_1080_02713683_2021_2002907
pubmed_primary_34738835
proquest_miscellaneous_2594297747
crossref_primary_10_1080_02713683_2021_2002907
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-04-03
PublicationDateYYYYMMDD 2022-04-03
PublicationDate_xml – month: 04
  year: 2022
  text: 2022-04-03
  day: 03
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Current eye research
PublicationTitleAlternate Curr Eye Res
PublicationYear 2022
Publisher Taylor & Francis
Publisher_xml – name: Taylor & Francis
References Naskar R (CIT0014) 2000; 41
CIT0020
CIT0012
CIT0011
Shpak AA (CIT0018) 2017; 23
Allison K (CIT0001) 2020; 12
Comparison of glaucomatous progression between untreated patients with normal-tension glaucoma and patients with therapeutically reduced intraocular pressures (CIT0003) 1998; 126
Wordinger RJ (CIT0010) 2003; 9
Harper MM (CIT0004) 2020; 46
CIT0002
CIT0013
Jiang C (CIT0015) 2007; 13
CIT0005
CIT0016
CIT0007
CIT0006
CIT0017
CIT0009
CIT0008
CIT0019
References_xml – ident: CIT0006
  doi: 10.1080/08977190410001715181
– ident: CIT0012
  doi: 10.1016/j.exer.2018.09.006
– volume: 13
  start-page: 1783
  year: 2007
  ident: CIT0015
  publication-title: Mol Vis
– ident: CIT0002
  doi: 10.1136/bjo.80.5.389
– ident: CIT0008
  doi: 10.1038/nrn812
– ident: CIT0011
  doi: 10.3390/cells9092082
– ident: CIT0019
  doi: 10.2337/diacare.25.6.1060
– volume: 126
  start-page: 487
  issue: 4
  year: 1998
  ident: CIT0003
  publication-title: Am J Ophthalmol
  doi: 10.1016/S0002-9394(98)00223-2
– ident: CIT0005
  doi: 10.1038/nrn2054
– ident: CIT0007
  doi: 10.1016/j.preteyeres.2011.11.005
– volume: 41
  start-page: 1940
  issue: 7
  year: 2000
  ident: CIT0014
  publication-title: Invest Ophthalmol Vis Sci
– ident: CIT0017
  doi: 10.1111/j.0953-816X.2003.03107.x
– volume: 12
  start-page: e11686
  issue: 11
  year: 2020
  ident: CIT0001
  publication-title: Cureus
– ident: CIT0013
  doi: 10.3390/ph14010050
– volume: 23
  start-page: 799
  year: 2017
  ident: CIT0018
  publication-title: Mol Vis
– volume: 46
  start-page: 1
  year: 2020
  ident: CIT0004
  publication-title: Curr Eye Res
– ident: CIT0009
  doi: 10.1167/iovs.14-15266
– volume: 9
  start-page: 249
  year: 2003
  ident: CIT0010
  publication-title: Mol Vis
– ident: CIT0020
  doi: 10.1006/exer.2001.1145
– ident: CIT0016
  doi: 10.1167/iovs.08-3013
SSID ssj0002714
Score 2.3410332
Snippet The purpose of this study was to examine the expression of glial-derived neurotrophic factor (GDNF), the GDNF receptors GFRα1 and GFRα2, ciliary neurotrophic...
SourceID proquest
pubmed
crossref
informaworld
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 597
SubjectTerms Ciliary Neurotrophic Factor - metabolism
Ciliary Neurotrophic Factor Receptor alpha Subunit - metabolism
CNTF
GDNF
glaucoma
Glaucoma - diagnosis
Glaucoma - metabolism
Glial Cell Line-Derived Neurotrophic Factor - metabolism
Glial Cell Line-Derived Neurotrophic Factor Receptors - metabolism
Humans
neuroprotection
neurotrophic growth factor
Retina - metabolism
Retinal Ganglion Cells - metabolism
Title Decreased Expression of Glial-Derived Neurotrophic Factor Receptors in Glaucomatous Human Retinas
URI https://www.tandfonline.com/doi/abs/10.1080/02713683.2021.2002907
https://www.ncbi.nlm.nih.gov/pubmed/34738835
https://www.proquest.com/docview/2594297747
Volume 47
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLZKJyFeEGxcxk1GQrxUqdLYcZLHjq5UE-OpSHuLbMehhZJUXYoo_4Z_yrHjuAkMxniJqiS-xOfrudjngtCriISRpER5MagTHk0E8-JExV4UipyImJJM6ODk8_ds9oGeXYQXvd6PltfSthJD-f3KuJL_oSrcA7rqKNkbUNZ1CjfgN9AXrkBhuP4TjSdG57sEnfH0m3VoNdrf2xWM7U1gCl_hmcm_UW3K9WIpB1NTX0dri2ptCu0sdVYNvoXp6erol25Xv1oW1nHoUzc_qdrpSiutTTANl8_bjXZjNJxGLJYfi72dX6q6diNw3GIwHjoOD9C0sf28yHaDmXvyTmXlytYLOSsXHCRBZ3MC7Frt00JaPCyIRh5hda2aoap5LGW-FwR-hwnXaTct2GiLo4a1-64VzszEaP_O962jJIymBwOzPzC2f5D40V7QNYf7v8g_55U4atKl2m5S3U1qu7mFDgKwRII-OhifTE6mTtzDyyZHWfOlTZiYTuB-1Xw6ClAnPe6fjRyj7MzvobvWSsHjGnL3UU8Vh-hoXABEvuzwa2z8hs2BzCG6fW7dM44Qd4DEe0DiMscdQOI2IHENSOwAiZcFbgMSG0BiC8gHaD49nb-ZebaGhycJY5XHdI6yPMmBAZCcKyJ9KvyRrzhjOWdKCEmlCHksmdRH9KAsCcm1VCFCBGFGHqJ-URbqMcJJHHCiaAjNOM0UiZnIeK6j8RgTIyKOEW3WNZU2v70us7JK_0rXYzR0zdZ1gpfrGiRtoqWV2VnL6zI4Kbmm7cuGwimwcX02xwsFa5kGYQKaIdhi8M6jmvRuOoRGBBYkfHLTqT5Fd_Z_ymeoX2226jno0JV4YVH8E1JOvGg
linkProvider EBSCOhost
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Decreased+Expression+of+Glial-Derived+Neurotrophic+Factor+Receptors+in+Glaucomatous+Human+Retinas&rft.jtitle=Current+eye+research&rft.au=Akurathi%2C+Abhigna&rft.au=Boese%2C+Erin+A.&rft.au=Kardon%2C+Randy+H.&rft.au=Ledolter%2C+Johannes&rft.date=2022-04-03&rft.issn=0271-3683&rft.eissn=1460-2202&rft.volume=47&rft.issue=4&rft.spage=597&rft.epage=605&rft_id=info:doi/10.1080%2F02713683.2021.2002907&rft.externalDBID=n%2Fa&rft.externalDocID=10_1080_02713683_2021_2002907
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0271-3683&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0271-3683&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0271-3683&client=summon