-
Je něco špatně v tomto záznamu ?
The protective effects of erythropoietin on rat glomerular podocytes in culture are modulated by extracellular matrix proteins
J. Krtil, J. Pláteník, N. Čuřík, W. Brima, V. Tesař, T. Zima,
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2013
Free Medical Journals
od 2010
ProQuest Central
od 1994-05-01 do Před 1 rokem
Open Access Digital Library
od 2013-01-01
Medline Complete (EBSCOhost)
od 2005-01-01
Health & Medicine (ProQuest)
od 1994-05-01 do Před 1 rokem
Karger Open Access
od 2013-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1996
PubMed
24685986
DOI
10.1159/000355762
Knihovny.cz E-zdroje
- MeSH
- barvicí látky MeSH
- erythropoetin farmakologie MeSH
- extracelulární matrix - proteiny fyziologie MeSH
- extracelulární matrix účinky léků metabolismus MeSH
- glomerulus účinky léků MeSH
- krysa rodu rattus MeSH
- kultivované buňky MeSH
- podocyty účinky léků MeSH
- primární buněčná kultura MeSH
- receptory erythropoetinu biosyntéza účinky léků MeSH
- rekombinantní proteiny farmakologie MeSH
- tetrazoliové soli MeSH
- thiazoly MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
BACKGROUND/AIMS: Podocytes are typically cultured on collagen I; however, collagen I is absent from healthy glomerular basement membranes. Erythropoietin (EPO) is thought to protect podocytes in vivo. Here, we studied how various types of extracellular matrix (ECM) proteins and EPO affect podocytes in culture. METHODS: Primary rat podocytes were replated on collagen I, collagen IV, whole ECM extract, laminin, or bare plastic. Cellular adhesion (8 hours after plating), proliferation (5 days, 10 % serum), and resistance to serum deprivation (3 days, 0.5 % serum) were assessed. BrdU incorporation and expression of podocyte-specific markers were employed as measures of cellular proliferation and differentiation, respectively. qPCR was used to verify expression of EPO receptor in cultured podocytes. RESULTS: Cellular adhesion was similar on all ECM proteins and unaffected by EPO. Proliferation was accelerated by laminin and the ECM extract, but the final cell density was similar on all ECM surfaces. Collagen IV supported the serum-deprived cells better than the other ECM proteins. EPO (2-20 ng/ml) improved viability of serum-deprived podocytes on collagen I, collagen IV, and ECM, but not on laminin or bare plastic. The cells expressed mRNA for EPO receptor. CONCLUSION: The physiological ECM proteins are more supportive of primary podocytic cultures compared with collagen I. The protective effects of EPO during serum deprivation are modulated by the cultivation surface.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15008635
- 003
- CZ-PrNML
- 005
- 20150327122705.0
- 007
- ta
- 008
- 150306s2013 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1159/000355762 $2 doi
- 035 __
- $a (PubMed)24685986
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Krtil, Jan $u Institute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
- 245 14
- $a The protective effects of erythropoietin on rat glomerular podocytes in culture are modulated by extracellular matrix proteins / $c J. Krtil, J. Pláteník, N. Čuřík, W. Brima, V. Tesař, T. Zima,
- 520 9_
- $a BACKGROUND/AIMS: Podocytes are typically cultured on collagen I; however, collagen I is absent from healthy glomerular basement membranes. Erythropoietin (EPO) is thought to protect podocytes in vivo. Here, we studied how various types of extracellular matrix (ECM) proteins and EPO affect podocytes in culture. METHODS: Primary rat podocytes were replated on collagen I, collagen IV, whole ECM extract, laminin, or bare plastic. Cellular adhesion (8 hours after plating), proliferation (5 days, 10 % serum), and resistance to serum deprivation (3 days, 0.5 % serum) were assessed. BrdU incorporation and expression of podocyte-specific markers were employed as measures of cellular proliferation and differentiation, respectively. qPCR was used to verify expression of EPO receptor in cultured podocytes. RESULTS: Cellular adhesion was similar on all ECM proteins and unaffected by EPO. Proliferation was accelerated by laminin and the ECM extract, but the final cell density was similar on all ECM surfaces. Collagen IV supported the serum-deprived cells better than the other ECM proteins. EPO (2-20 ng/ml) improved viability of serum-deprived podocytes on collagen I, collagen IV, and ECM, but not on laminin or bare plastic. The cells expressed mRNA for EPO receptor. CONCLUSION: The physiological ECM proteins are more supportive of primary podocytic cultures compared with collagen I. The protective effects of EPO during serum deprivation are modulated by the cultivation surface.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a kultivované buňky $7 D002478
- 650 _2
- $a barvicí látky $7 D004396
- 650 _2
- $a erythropoetin $x farmakologie $7 D004921
- 650 _2
- $a extracelulární matrix $x účinky léků $x metabolismus $7 D005109
- 650 _2
- $a extracelulární matrix - proteiny $x fyziologie $7 D016326
- 650 _2
- $a glomerulus $x účinky léků $7 D007678
- 650 _2
- $a podocyty $x účinky léků $7 D050199
- 650 _2
- $a primární buněčná kultura $7 D061251
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a receptory erythropoetinu $x biosyntéza $x účinky léků $7 D017467
- 650 _2
- $a rekombinantní proteiny $x farmakologie $7 D011994
- 650 _2
- $a tetrazoliové soli $7 D013778
- 650 _2
- $a thiazoly $7 D013844
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Pláteník, Jan
- 700 1_
- $a Čuřík, Nikola
- 700 1_
- $a Brima, Wunnie
- 700 1_
- $a Tesař, Vladimír
- 700 1_
- $a Zima, Tomáš
- 773 0_
- $w MED00003064 $t Kidney & blood pressure research $x 1423-0143 $g Roč. 38, č. 1 (2013), s. 142-55
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24685986 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20150306 $b ABA008
- 991 __
- $a 20150327123027 $b ABA008
- 999 __
- $a ok $b bmc $g 1065908 $s 891435
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2013 $b 38 $c 1 $d 142-55 $i 1423-0143 $m Kidney & blood pressure research $n Kidney Blood Press Res $x MED00003064
- LZP __
- $a Pubmed-20150306