-
Je něco špatně v tomto záznamu ?
Membrane and soluble endoglin role in cardiovascular and metabolic disorders related to metabolic syndrome
M. Vicen, IC. Igreja Sá, K. Tripská, B. Vitverová, I. Najmanová, S. Eissazadeh, S. Micuda, P. Nachtigal
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, přehledy
Grantová podpora
. CZ.02.1.01/0.0/0.0/16_019/0000841
EFSA-CDN
SVV 260 549
FP7 Research Potential of Convergence Regions ()
1130120
Grantová Agentura, Univerzita Karlova
1166119
Grantová Agentura, Univerzita Karlova
17-31754A
Agentura Pro Zdravotnický Výzkum České Republiky
NV17-31754A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
NLK
PubMed Central
od 1997
ProQuest Central
od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2000-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-01-01 do Před 1 rokem
Springer Nature OA/Free Journals
od 1945-04-01
- MeSH
- ateroskleróza metabolismus patologie MeSH
- biologické markery metabolismus MeSH
- buněčná membrána metabolismus MeSH
- diabetes mellitus 2. typu metabolismus patologie MeSH
- endoglin chemie metabolismus MeSH
- exprese genu MeSH
- kardiovaskulární nemoci metabolismus patologie MeSH
- lidé MeSH
- metabolický syndrom metabolismus patologie MeSH
- synthasa oxidu dusnatého, typ III metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Membrane endoglin (Eng, CD105) is a transmembrane glycoprotein essential for the proper function of vascular endothelium. It might be cleaved by matrix metalloproteinases to form soluble endoglin (sEng), which is released into the circulation. Metabolic syndrome comprises conditions/symptoms that usually coincide (endothelial dysfunction, arterial hypertension, hyperglycemia, obesity-related insulin resistance, and hypercholesterolemia), and are considered risk factors for cardiometabolic disorders such as atherosclerosis, type II diabetes mellitus, and liver disorders. The purpose of this review is to highlight current knowledge about the role of Eng and sEng in the disorders mentioned above, in vivo and in vitro extent, where we can find a wide range of contradictory results. We propose that reduced Eng expression is a hallmark of endothelial dysfunction development in chronic pathologies related to metabolic syndrome. Eng expression is also essential for leukocyte transmigration and acute inflammation, suggesting that Eng is crucial for the regulation of endothelial function during the acute phase of vascular defense reaction to harmful conditions. sEng was shown to be a circulating biomarker of preeclampsia, and we propose that it might be a biomarker of metabolic syndrome-related symptoms and pathologies, including hypercholesterolemia, hyperglycemia, arterial hypertension, and diabetes mellitus as well, despite the fact that some contradictory findings have been reported. Besides, sEng can participate in the development of endothelial dysfunction and promote the development of arterial hypertension, suggesting that high levels of sEng promote metabolic syndrome symptoms and complications. Therefore, we suggest that the treatment of metabolic syndrome should take into account the importance of Eng in the endothelial function and levels of sEng as a biomarker and risk factor of related pathologies.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21019122
- 003
- CZ-PrNML
- 005
- 20210830100713.0
- 007
- ta
- 008
- 210728s2021 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s00018-020-03701-w $2 doi
- 035 __
- $a (PubMed)33185696
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Vicen, Matej $u Faculty of Pharmacy in Hradec Kralove, Department of Biological and Medical Sciences, Charles University, Heyrovskeho 1203, Hradec Kralove, 500 03, Czech Republic
- 245 10
- $a Membrane and soluble endoglin role in cardiovascular and metabolic disorders related to metabolic syndrome / $c M. Vicen, IC. Igreja Sá, K. Tripská, B. Vitverová, I. Najmanová, S. Eissazadeh, S. Micuda, P. Nachtigal
- 520 9_
- $a Membrane endoglin (Eng, CD105) is a transmembrane glycoprotein essential for the proper function of vascular endothelium. It might be cleaved by matrix metalloproteinases to form soluble endoglin (sEng), which is released into the circulation. Metabolic syndrome comprises conditions/symptoms that usually coincide (endothelial dysfunction, arterial hypertension, hyperglycemia, obesity-related insulin resistance, and hypercholesterolemia), and are considered risk factors for cardiometabolic disorders such as atherosclerosis, type II diabetes mellitus, and liver disorders. The purpose of this review is to highlight current knowledge about the role of Eng and sEng in the disorders mentioned above, in vivo and in vitro extent, where we can find a wide range of contradictory results. We propose that reduced Eng expression is a hallmark of endothelial dysfunction development in chronic pathologies related to metabolic syndrome. Eng expression is also essential for leukocyte transmigration and acute inflammation, suggesting that Eng is crucial for the regulation of endothelial function during the acute phase of vascular defense reaction to harmful conditions. sEng was shown to be a circulating biomarker of preeclampsia, and we propose that it might be a biomarker of metabolic syndrome-related symptoms and pathologies, including hypercholesterolemia, hyperglycemia, arterial hypertension, and diabetes mellitus as well, despite the fact that some contradictory findings have been reported. Besides, sEng can participate in the development of endothelial dysfunction and promote the development of arterial hypertension, suggesting that high levels of sEng promote metabolic syndrome symptoms and complications. Therefore, we suggest that the treatment of metabolic syndrome should take into account the importance of Eng in the endothelial function and levels of sEng as a biomarker and risk factor of related pathologies.
- 650 _2
- $a ateroskleróza $x metabolismus $x patologie $7 D050197
- 650 _2
- $a biologické markery $x metabolismus $7 D015415
- 650 _2
- $a kardiovaskulární nemoci $x metabolismus $x patologie $7 D002318
- 650 _2
- $a buněčná membrána $x metabolismus $7 D002462
- 650 _2
- $a diabetes mellitus 2. typu $x metabolismus $x patologie $7 D003924
- 650 _2
- $a endoglin $x chemie $x metabolismus $7 D000071063
- 650 _2
- $a exprese genu $7 D015870
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a metabolický syndrom $x metabolismus $x patologie $7 D024821
- 650 _2
- $a synthasa oxidu dusnatého, typ III $x metabolismus $7 D052250
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Igreja Sá, Ivone Cristina $u Faculty of Pharmacy in Hradec Kralove, Department of Biological and Medical Sciences, Charles University, Heyrovskeho 1203, Hradec Kralove, 500 03, Czech Republic
- 700 1_
- $a Tripská, Katarína $u Faculty of Pharmacy in Hradec Kralove, Department of Biological and Medical Sciences, Charles University, Heyrovskeho 1203, Hradec Kralove, 500 03, Czech Republic
- 700 1_
- $a Vitverová, Barbora $u Faculty of Pharmacy in Hradec Kralove, Department of Biological and Medical Sciences, Charles University, Heyrovskeho 1203, Hradec Kralove, 500 03, Czech Republic
- 700 1_
- $a Najmanová, Iveta $u Faculty of Pharmacy in Hradec Kralove, Department of Biological and Medical Sciences, Charles University, Heyrovskeho 1203, Hradec Kralove, 500 03, Czech Republic
- 700 1_
- $a Eissazadeh, Samira $u Faculty of Pharmacy in Hradec Kralove, Department of Biological and Medical Sciences, Charles University, Heyrovskeho 1203, Hradec Kralove, 500 03, Czech Republic
- 700 1_
- $a Micuda, Stanislav $u Faculty of Medicine in Hradec Kralove, Department of Pharmacology, Charles University, Simkova 870, Hradec Kralove, 500 03, Czech Republic
- 700 1_
- $a Nachtigal, Petr $u Faculty of Pharmacy in Hradec Kralove, Department of Biological and Medical Sciences, Charles University, Heyrovskeho 1203, Hradec Kralove, 500 03, Czech Republic. petr.nachtigal@faf.cuni.cz
- 773 0_
- $w MED00001078 $t Cellular and molecular life sciences : CMLS $x 1420-9071 $g Roč. 78, č. 6 (2021), s. 2405-2418
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33185696 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20210830100714 $b ABA008
- 999 __
- $a ok $b bmc $g 1690040 $s 1139568
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 78 $c 6 $d 2405-2418 $e 20201113 $i 1420-9071 $m Cellular and molecular life sciences $n Cell Mol Life Sci $x MED00001078
- GRA __
- $a . CZ.02.1.01/0.0/0.0/16_019/0000841 $p EFSA-CDN
- GRA __
- $a SVV 260 549 $p FP7 Research Potential of Convergence Regions ()
- GRA __
- $a 1130120 $p Grantová Agentura, Univerzita Karlova
- GRA __
- $a 1166119 $p Grantová Agentura, Univerzita Karlova
- GRA __
- $a 17-31754A $p Agentura Pro Zdravotnický Výzkum České Republiky
- GRA __
- $a NV17-31754A $p MZ0
- LZP __
- $a Pubmed-20210728