MESOTHELIAL CELLS
Department of Medicine, University of Hong Kong, Hong Kong SAR, PR China Correspondence to: S. Yung, Department of Medicine, Room 302, New Clinical Building, Queen Mary Hospital, Pokfulam, Hong Kong SAR, PR China. ssyyung{at}hkucc.hku.hk Background : The introduction of peritoneal dialysis (PD) as a...
Saved in:
Published in | Peritoneal dialysis international Vol. 27; no. Supplement_2; pp. S110 - 115 |
---|---|
Main Authors | , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
Milton, ON
Multimed
01.06.2007
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Department of Medicine, University of Hong Kong, Hong Kong SAR, PR
China
Correspondence to: S. Yung, Department of Medicine, Room 302, New Clinical
Building, Queen Mary Hospital, Pokfulam, Hong Kong SAR, PR China.
ssyyung{at}hkucc.hku.hk
Background : The introduction of peritoneal dialysis
(PD) as a modality of renal replacement therapy has provoked much interest in
the biology of the peritoneal mesothelial cell. Mesothelial cells isolated
from omental tissue have immunohistochemical markers that are identical to
those of mesothelial stem cells, and omental mesothelial cells can be
cultivated in vitro to study changes to their biologic functions in
the setting of PD.
Method : The present article describes the structure and
function of mesothelial cells in the normal peritoneum and details the
morphologic changes that occur after the introduction of PD. Furthermore, this
article reviews the literature of mesothelial cell culture and the limitations
of in vitro studies.
Results : The mesothelium is now considered to be a
dynamic membrane that plays a pivotal role in the homeostasis of the
peritoneal cavity, contributing to the control of fluid and solute transport,
inflammation, and wound healing. These functional properties of the
mesothelium are compromised in the setting of PD. Cultures of peritoneal
mesothelial cells from omental tissue provide a relevant in vitro
model that allows researchers to assess specific molecular pathways of disease
in a distinct population of cells. Structural and functional attributes of
mesothelial cells are discussed in relation to long-term culture,
proliferation potential, age of tissue donor, use of human or animal in
vitro models, and how the foregoing factors may influence in
vitro data.
Conclusions : The ability to propagate mesothelial cells
in culture has resulted, over the past two decades, in an explosion of
mesothelial cell research pertaining to PD and peritoneal disorders.
Independent researchers have highlighted the potential use of mesothelial
cells as targets for gene therapy or transplantation in the search to provide
therapeutic strategies for the preservation of the mesothelium during chemical
or bacterial injury.
KEY WORDS: Mesothelial cells; omentum; peritoneum; senescence; proliferation. |
---|---|
AbstractList | ♦ Background The introduction of peritoneal dialysis (PD) as a modality of renal replacement therapy has provoked much interest in the biology of the peritoneal mesothelial cell. Mesothelial cells isolated from omental tissue have immunohistochemical markers that are identical to those of mesothelial stem cells, and omental mesothelial cells can be cultivated in vitro to study changes to their biologic functions in the setting of PD. ♦ Method The present article describes the structure and function of mesothelial cells in the normal peritoneum and details the morphologic changes that occur after the introduction of PD. Furthermore, this article reviews the literature of mesothelial cell culture and the limitations of in vitro studies. ♦ Results The mesothelium is now considered to be a dynamic membrane that plays a pivotal role in the homeostasis of the peritoneal cavity, contributing to the control of fluid and solute transport, inflammation, and wound healing. These functional properties of the mesothelium are compromised in the setting of PD. Cultures of peritoneal mesothelial cells from omental tissue provide a relevant in vitro model that allows researchers to assess specific molecular pathways of disease in a distinct population of cells. Structural and functional attributes of mesothelial cells are discussed in relation to long-term culture, proliferation potential, age of tissue donor, use of human or animal in vitro models, and how the foregoing factors may influence in vitro data. ♦ Conclusions The ability to propagate mesothelial cells in culture has resulted, over the past two decades, in an explosion of mesothelial cell research pertaining to PD and peritoneal disorders. Independent researchers have highlighted the potential use of mesothelial cells as targets for gene therapy or transplantation in the search to provide therapeutic strategies for the preservation of the mesothelium during chemical or bacterial injury. Department of Medicine, University of Hong Kong, Hong Kong SAR, PR China Correspondence to: S. Yung, Department of Medicine, Room 302, New Clinical Building, Queen Mary Hospital, Pokfulam, Hong Kong SAR, PR China. ssyyung{at}hkucc.hku.hk Background : The introduction of peritoneal dialysis (PD) as a modality of renal replacement therapy has provoked much interest in the biology of the peritoneal mesothelial cell. Mesothelial cells isolated from omental tissue have immunohistochemical markers that are identical to those of mesothelial stem cells, and omental mesothelial cells can be cultivated in vitro to study changes to their biologic functions in the setting of PD. Method : The present article describes the structure and function of mesothelial cells in the normal peritoneum and details the morphologic changes that occur after the introduction of PD. Furthermore, this article reviews the literature of mesothelial cell culture and the limitations of in vitro studies. Results : The mesothelium is now considered to be a dynamic membrane that plays a pivotal role in the homeostasis of the peritoneal cavity, contributing to the control of fluid and solute transport, inflammation, and wound healing. These functional properties of the mesothelium are compromised in the setting of PD. Cultures of peritoneal mesothelial cells from omental tissue provide a relevant in vitro model that allows researchers to assess specific molecular pathways of disease in a distinct population of cells. Structural and functional attributes of mesothelial cells are discussed in relation to long-term culture, proliferation potential, age of tissue donor, use of human or animal in vitro models, and how the foregoing factors may influence in vitro data. Conclusions : The ability to propagate mesothelial cells in culture has resulted, over the past two decades, in an explosion of mesothelial cell research pertaining to PD and peritoneal disorders. Independent researchers have highlighted the potential use of mesothelial cells as targets for gene therapy or transplantation in the search to provide therapeutic strategies for the preservation of the mesothelium during chemical or bacterial injury. KEY WORDS: Mesothelial cells; omentum; peritoneum; senescence; proliferation. BACKGROUNDThe introduction of peritoneal dialysis (PD) as a modality of renal replacement therapy has provoked much interest in the biology of the peritoneal mesothelial cell. Mesothelial cells isolated from omental tissue have immunohistochemical markers that are identical to those of mesothelial stem cells, and omental mesothelial cells can be cultivated in vitro to study changes to their biologic functions in the setting of PD. METHODThe present article describes the structure and function of mesothelial cells in the normal peritoneum and details the morphologic changes that occur after the introduction of PD. Furthermore, this article reviews the literature of mesothelial cell culture and the limitations of in vitro studies. RESULTSThe mesothelium is now considered to be a dynamic membrane that plays a pivotal role in the homeostasis of the peritoneal cavity, contributing to the control of fluid and solute transport, inflammation, and wound healing. These functional properties of the mesothelium are compromised in the setting of PD. Cultures of peritoneal mesothelial cells from omental tissue provide a relevant in vitro model that allows researchers to assess specific molecular pathways of disease in a distinct population of cells. Structural and functional attributes of mesothelial cells are discussed in relation to long-term culture, proliferation potential, age of tissue donor, use of human or animal in vitro models, and how the foregoing factors may influence in vitro data. CONCLUSIONSThe ability to propagate mesothelial cells in culture has resulted, over the past two decades, in an explosion of mesothelial cell research pertaining to PD and peritoneal disorders. Independent researchers have highlighted the potential use of mesothelial cells as targets for gene therapy or transplantation in the search to provide therapeutic strategies for the preservation of the mesothelium during chemical or bacterial injury. The introduction of peritoneal dialysis (PD) as a modality of renal replacement therapy has provoked much interest in the biology of the peritoneal mesothelial cell. Mesothelial cells isolated from omental tissue have immunohistochemical markers that are identical to those of mesothelial stem cells, and omental mesothelial cells can be cultivated in vitro to study changes to their biologic functions in the setting of PD. The present article describes the structure and function of mesothelial cells in the normal peritoneum and details the morphologic changes that occur after the introduction of PD. Furthermore, this article reviews the literature of mesothelial cell culture and the limitations of in vitro studies. The mesothelium is now considered to be a dynamic membrane that plays a pivotal role in the homeostasis of the peritoneal cavity, contributing to the control of fluid and solute transport, inflammation, and wound healing. These functional properties of the mesothelium are compromised in the setting of PD. Cultures of peritoneal mesothelial cells from omental tissue provide a relevant in vitro model that allows researchers to assess specific molecular pathways of disease in a distinct population of cells. Structural and functional attributes of mesothelial cells are discussed in relation to long-term culture, proliferation potential, age of tissue donor, use of human or animal in vitro models, and how the foregoing factors may influence in vitro data. The ability to propagate mesothelial cells in culture has resulted, over the past two decades, in an explosion of mesothelial cell research pertaining to PD and peritoneal disorders. Independent researchers have highlighted the potential use of mesothelial cells as targets for gene therapy or transplantation in the search to provide therapeutic strategies for the preservation of the mesothelium during chemical or bacterial injury. |
Author | Yung, Susan Chan, Tak Mao |
Author_xml | – sequence: 1 fullname: Yung, Susan – sequence: 2 fullname: Chan, Tak Mao |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19942517$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/17556288$$D View this record in MEDLINE/PubMed |
BookMark | eNpl0EtLw0AQB_BFKvahB68exIveovvMZo-lRFuI9JB6XjbJrI3kZbYh-O2b0kAPwjBz-c0fZuZoUtUVIPRA8CshUr7hQPmBjwMsMR3KEXWFZkSSwOMM8wmanYB3ElM0d-4HY0YZljdoSqQQPg2CGbr_DOPtbh1Gm2X0tAqjKL5F19YUDu7GuUBf7-Futfai7cdmtYy8lDN18BizCYBMrGUWKDfGkizzrcSWMWqGLrgSIgPgkFCbMOqnQFWqjMECGABboJdzbtPWvx24gy5zl0JRmArqzmmJhZJC8gHSM0zb2rkWrG7avDTtnyZYnx6h_z9iWHoc07ukhOyyMl4-gOcRGJeawramSnN3cUpxKogcHDm7ff697_MWtCtNUQyxVPd9T6WOu6YpoITqoKmOCcHsCLmDdqU |
CitedBy_id | crossref_primary_10_3747_pdi_2012_00323 crossref_primary_10_1007_s00464_010_1139_2 crossref_primary_10_1177_0192623313501894 crossref_primary_10_1002_ar_22607 crossref_primary_10_1245_s10434_015_4508_1 crossref_primary_10_3390_jdb1020064 crossref_primary_10_1038_cddis_2016_79 crossref_primary_10_4049_jimmunol_2200278 crossref_primary_10_1016_j_bbamcr_2014_12_025 crossref_primary_10_1097_GOX_0000000000004528 crossref_primary_10_1016_j_cyto_2017_02_021 crossref_primary_10_1186_s12893_020_00775_y crossref_primary_10_1016_j_soc_2018_02_003 crossref_primary_10_1016_j_amjsurg_2009_08_031 crossref_primary_10_1016_j_tice_2016_11_004 crossref_primary_10_3389_fphys_2014_00412 crossref_primary_10_1002_cam4_159 crossref_primary_10_1155_2011_180594 crossref_primary_10_1016_j_tem_2015_07_003 crossref_primary_10_1016_j_neo_2019_08_006 crossref_primary_10_1371_journal_pone_0069712 crossref_primary_10_1016_j_path_2010_03_010 crossref_primary_10_3389_fcell_2022_1025240 crossref_primary_10_3109_0886022X_2013_773915 crossref_primary_10_1080_17425247_2020_1736551 crossref_primary_10_3747_pdi_2014_00188 crossref_primary_10_1016_j_cyto_2015_11_010 crossref_primary_10_1007_s00467_012_2120_1 crossref_primary_10_1371_journal_pone_0079678 crossref_primary_10_1016_j_arr_2013_01_008 crossref_primary_10_1067_j_cpsurg_2015_05_001 crossref_primary_10_1134_S2079086416060025 crossref_primary_10_1002_jcb_24642 crossref_primary_10_1016_j_lfs_2016_07_018 crossref_primary_10_1097_MD_0000000000010450 crossref_primary_10_1186_s12929_016_0232_9 crossref_primary_10_1002_dvdy_23855 crossref_primary_10_3390_nano14010004 crossref_primary_10_1134_S0022093020010068 crossref_primary_10_3390_ijms17101611 crossref_primary_10_1158_0008_5472_CAN_16_0964 crossref_primary_10_1111_j_1525_1594_2009_00735_x crossref_primary_10_1016_j_jmig_2014_03_015 crossref_primary_10_1016_j_aquatox_2016_02_018 crossref_primary_10_3390_ijms222212443 crossref_primary_10_1007_s10157_017_1440_7 crossref_primary_10_1016_j_hkjn_2013_09_002 crossref_primary_10_1007_s00404_015_3717_y crossref_primary_10_3747_pdi_2012_00148 crossref_primary_10_1016_j_ebiom_2020_102661 crossref_primary_10_1007_s00383_009_2503_y crossref_primary_10_1038_s41598_019_44219_x |
Cites_doi | 10.1172/JCI17129 10.1046/j.1523-1755.2003.00861.x 10.1002/aja.1001490111 10.1681/ASN.V13suppl_1s117 10.1681/ASN.V133721 10.1002/ar.1091770307 10.1007/BF00235068 10.1177/089686080202200202 10.1093/ndt/gfl271 10.1006/mvre.1997.2039 10.1046/j.1523-1755.1998.00177.x 10.1177/089686089101100106 10.1002/path.1711450204 10.1055/s-2007-1006424 10.1046/j.1440-1843.2002.00404.x 10.1177/089686080602600207 10.1111/j.1523-1755.2000.00367.x 10.1101/gad.859201 10.1093/ndt/gfl355 10.1097/01.ASN.0000122826.40921.D7 10.1111/j.1523-1755.2005.00698.x 10.1016/j.cellbi.2003.11.010 10.1159/000183987 10.1038/sj.ki.5000082 10.1056/NEJMoa020809 10.1016/j.biocel.2003.11.002 10.1046/j.1523-1755.2003.08805.x 10.1159/000186214 10.1007/s10151-006-0268-z 10.1159/000184872 10.1038/nbt0702-675 10.1152/japplphysiol.01086.2005 10.1046/j.1523-1755.1998.00174.x 10.1038/ki.1990.150 |
ContentType | Journal Article Conference Proceeding |
Copyright | 2008 INIST-CNRS |
Copyright_xml | – notice: 2008 INIST-CNRS |
DBID | IQODW CGR CUY CVF ECM EIF NPM AAYXX CITATION 7X8 |
DOI | 10.1177/089686080702702s19 |
DatabaseName | Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed CrossRef MEDLINE - Academic |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) CrossRef MEDLINE - Academic |
DatabaseTitleList | CrossRef 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 |
EISSN | 1718-4304 |
EndPage | 115 |
ExternalDocumentID | 10_1177_089686080702702s19 17556288 19942517 www27_Supplement_2_S110 |
Genre | Research Support, Non-U.S. Gov't Journal Article Review |
GroupedDBID | - 123 5RE AANGY ADACO AENEX AGCAB AIOMO AJUZI ALMA_UNASSIGNED_HOLDINGS ARTOV BBRGL BKIIM BWJAD DC- DIK DOPDO DU5 E3Z EBS EJD F5P GJ GROUPED_SAGE_PREMIER_JOURNAL_COLLECTION GX1 H13 J8X KQ8 OK1 P2P R0Z RHF RHI RPM SFC TMM --- .GJ 18M 53G AACMV AADUE AAGGD AAGHA AAKGS AAMXZ AARIX AAZBJ ABDWY ABJOC ABKRH ABLUO ABLYK ABSGY ABYTW ACARO ACFEJ ACFMA ACGFO ACLDX ACLFY ACLHI ACOFE ACROE ACSIQ ACUAV ACXKE ACXMB ADBBV ADEIA ADMPF ADRRZ AEGXH AESZF AEWHI AFKRG AFMOU AFQAA AFUIA AGHDM AGNHF AIAGR AJEFB AJXAJ ANDLU AOIJS BAWUL BPACV CBRKF CDWPY CFDXU CORYS CQQTX CUTAK CWQVV CYONA DCPMT EMOBN HYE IQODW JCYGO M4V Q1R SAFTQ SCNPE TR2 W8F XVB ZONMY ZPPRI ZRKOI 0R~ AABMB AAEWN AATAA ABPNF ABRHV ACJER ACOXC ACUIR ADUKL AEXNY AGKLV ALKWR ALTZF CGR CUY CVF ECM EIF FHBDP NPM AAYXX CITATION 7X8 |
ID | FETCH-LOGICAL-c439t-33fbee7bff3fe24aaf1dd6f70f332a0f354955dee4eb2fb326ce29c9aa05e3ee3 |
ISSN | 0896-8608 |
IngestDate | Sun Sep 29 07:15:40 EDT 2024 Wed Oct 09 16:51:12 EDT 2024 Sat Sep 28 08:31:52 EDT 2024 Sun Oct 22 16:06:05 EDT 2023 Tue Jan 05 20:17:11 EST 2021 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | Supplement_2 |
Keywords | Kidney disease Extrarenal dialysis Senescence Urinary system disease Mesothelial cells proliferation Renal failure Omentum Peritoneal dialysis Peritoneum |
Language | English |
License | CC BY 4.0 |
LinkModel | OpenURL |
MeetingName | Proceedings of the ISPD 2006: proceedings of the 11th Congress of the International Society for Peritoneal Dialysis, Achieving PD Excellence, Hong Kong, August 25-August 29, 2006 |
MergedId | FETCHMERGED-LOGICAL-c439t-33fbee7bff3fe24aaf1dd6f70f332a0f354955dee4eb2fb326ce29c9aa05e3ee3 |
Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
PMID | 17556288 |
PQID | 70597574 |
PQPubID | 23479 |
PageCount | 6 |
ParticipantIDs | proquest_miscellaneous_70597574 crossref_primary_10_1177_089686080702702s19 pubmed_primary_17556288 pascalfrancis_primary_19942517 highwire_smallpub2_www27_Supplement_2_S110 |
ProviderPackageCode | RHF RHI |
PublicationCentury | 2000 |
PublicationDate | 2007-06-01 |
PublicationDateYYYYMMDD | 2007-06-01 |
PublicationDate_xml | – month: 06 year: 2007 text: 2007-06-01 day: 01 |
PublicationDecade | 2000 |
PublicationPlace | Milton, ON |
PublicationPlace_xml | – name: Milton, ON – name: United States |
PublicationTitle | Peritoneal dialysis international |
PublicationTitleAlternate | Perit Dial Int |
PublicationYear | 2007 |
Publisher | Multimed |
Publisher_xml | – name: Multimed |
References | bibr27-089686080702702s19 Mather JP (bibr26-089686080702702s19) 1998 bibr25-089686080702702s19 bibr24-089686080702702s19 bibr28-089686080702702s19 Yung S (bibr8-089686080702702s19) 1995; 146 bibr29-089686080702702s19 Nagy JA (bibr1-089686080702702s19) 1996; 50 bibr34-089686080702702s19 bibr5-089686080702702s19 bibr4-089686080702702s19 bibr3-089686080702702s19 bibr36-089686080702702s19 bibr35-089686080702702s19 bibr37-089686080702702s19 bibr7-089686080702702s19 bibr2-089686080702702s19 bibr31-089686080702702s19 bibr32-089686080702702s19 bibr6-089686080702702s19 bibr30-089686080702702s19 bibr9-089686080702702s19 bibr14-089686080702702s19 bibr15-089686080702702s19 bibr38-089686080702702s19 bibr18-089686080702702s19 bibr16-089686080702702s19 bibr17-089686080702702s19 bibr10-089686080702702s19 bibr13-089686080702702s19 bibr11-089686080702702s19 bibr12-089686080702702s19 bibr22-089686080702702s19 bibr23-089686080702702s19 bibr19-089686080702702s19 bibr21-089686080702702s19 bibr20-089686080702702s19 Piano G (bibr33-089686080702702s19) 1998; 64 |
References_xml | – ident: bibr11-089686080702702s19 doi: 10.1172/JCI17129 – ident: bibr30-089686080702702s19 doi: 10.1046/j.1523-1755.2003.00861.x – ident: bibr4-089686080702702s19 doi: 10.1002/aja.1001490111 – start-page: 151 volume-title: Introduction to Cell and Tissue Culture: Theory and Technique year: 1998 ident: bibr26-089686080702702s19 contributor: fullname: Mather JP – ident: bibr36-089686080702702s19 doi: 10.1681/ASN.V13suppl_1s117 – volume: 64 start-page: 424 year: 1998 ident: bibr33-089686080702702s19 publication-title: Am Surg contributor: fullname: Piano G – ident: bibr37-089686080702702s19 doi: 10.1681/ASN.V133721 – ident: bibr5-089686080702702s19 doi: 10.1002/ar.1091770307 – volume: 50 start-page: S2 issue: 56 year: 1996 ident: bibr1-089686080702702s19 publication-title: Kidney Int contributor: fullname: Nagy JA – ident: bibr3-089686080702702s19 doi: 10.1007/BF00235068 – ident: bibr10-089686080702702s19 doi: 10.1177/089686080202200202 – ident: bibr31-089686080702702s19 doi: 10.1093/ndt/gfl271 – ident: bibr21-089686080702702s19 doi: 10.1006/mvre.1997.2039 – ident: bibr29-089686080702702s19 doi: 10.1046/j.1523-1755.1998.00177.x – ident: bibr28-089686080702702s19 doi: 10.1177/089686089101100106 – ident: bibr18-089686080702702s19 doi: 10.1002/path.1711450204 – ident: bibr34-089686080702702s19 doi: 10.1055/s-2007-1006424 – ident: bibr2-089686080702702s19 doi: 10.1046/j.1440-1843.2002.00404.x – ident: bibr20-089686080702702s19 doi: 10.1177/089686080602600207 – ident: bibr9-089686080702702s19 doi: 10.1111/j.1523-1755.2000.00367.x – ident: bibr23-089686080702702s19 doi: 10.1101/gad.859201 – ident: bibr32-089686080702702s19 doi: 10.1093/ndt/gfl355 – ident: bibr15-089686080702702s19 doi: 10.1097/01.ASN.0000122826.40921.D7 – ident: bibr38-089686080702702s19 doi: 10.1111/j.1523-1755.2005.00698.x – volume: 146 start-page: 520 year: 1995 ident: bibr8-089686080702702s19 publication-title: Am J Pathol contributor: fullname: Yung S – ident: bibr6-089686080702702s19 doi: 10.1016/j.cellbi.2003.11.010 – ident: bibr16-089686080702702s19 doi: 10.1159/000183987 – ident: bibr25-089686080702702s19 doi: 10.1038/sj.ki.5000082 – ident: bibr27-089686080702702s19 doi: 10.1056/NEJMoa020809 – ident: bibr7-089686080702702s19 doi: 10.1016/j.biocel.2003.11.002 – ident: bibr17-089686080702702s19 doi: 10.1046/j.1523-1755.2003.08805.x – ident: bibr14-089686080702702s19 doi: 10.1159/000186214 – ident: bibr35-089686080702702s19 doi: 10.1007/s10151-006-0268-z – ident: bibr13-089686080702702s19 doi: 10.1159/000184872 – ident: bibr22-089686080702702s19 doi: 10.1038/nbt0702-675 – ident: bibr24-089686080702702s19 doi: 10.1152/japplphysiol.01086.2005 – ident: bibr12-089686080702702s19 doi: 10.1046/j.1523-1755.1998.00174.x – ident: bibr19-089686080702702s19 doi: 10.1038/ki.1990.150 |
SSID | ssj0032307 ssib044964478 |
Score | 2.1000485 |
SecondaryResourceType | review_article |
Snippet | Department of Medicine, University of Hong Kong, Hong Kong SAR, PR
China
Correspondence to: S. Yung, Department of Medicine, Room 302, New Clinical
Building,... The introduction of peritoneal dialysis (PD) as a modality of renal replacement therapy has provoked much interest in the biology of the peritoneal mesothelial... ♦ Background The introduction of peritoneal dialysis (PD) as a modality of renal replacement therapy has provoked much interest in the biology of the... BACKGROUNDThe introduction of peritoneal dialysis (PD) as a modality of renal replacement therapy has provoked much interest in the biology of the peritoneal... |
SourceID | proquest crossref pubmed pascalfrancis highwire |
SourceType | Aggregation Database Index Database Publisher |
StartPage | S110 |
SubjectTerms | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Biological and medical sciences Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis Cell Culture Techniques Cell Differentiation Emergency and intensive care: renal failure. Dialysis management Epithelial Cells - physiology Fundamental and applied biological sciences. Psychology Humans Intensive care medicine Intestine. Mesentery Kidney Failure, Chronic - pathology Kidney Failure, Chronic - therapy Medical sciences Peritoneal Dialysis Peritoneum - cytology Transfusions. Complications. Transfusion reactions. Cell and gene therapy Vertebrates: digestive system |
Title | MESOTHELIAL CELLS |
URI | http://www.pdiconnect.com/cgi/content/abstract/27/Supplement_2/S110 https://www.ncbi.nlm.nih.gov/pubmed/17556288 https://search.proquest.com/docview/70597574 |
Volume | 27 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fSyMxEB68CnJv_na9U_vgk2WPNskmu4-lVIu2KthCfQrZbQKCVrGVwv31N8n-6loP0ZewLCS7zBcmM8k3XwBOQ465sabM5zFjPrPpTmg4ZimJSkkYKrH7HYNr3huxy3EwLlUWXXXJPP6T_P2wruQ7qOI7xNVWyX4B2WJQfIHPiC-2iDC2qxh_uNTc4mesnLY7asnkRR6WN_mWp8Sge3cz7HUxe-83Ot1-v4gD70dp5VKFojNsXzUG7ZtGp5cJvuZ7A6LkMKX8IMtJfKoUSYUR90PeDJcdYFqcv-pL3Wmu7WE7oGuwpWuzzMFVhKvfLSgFzc_qDltJtB-wTmgUWKdzMS4YONRy0F2Qn_1TXtNk9bBWvlqNG3ItZ0tlVTOczSa9huT_eYKLF4absFtWUtZvC-C2YE1Pt2FjkBEadmBzCZO6w2QXRufdYafnZ7dU-AkGc3OfUhNrLWJjqNGEKWVakwk3omkoJQpbzMCDYKI10zExMYbLiSZREinVDDTVmu5BbYoT5QDqirUiwwQJTUgYj0SM7lGhw8S0mIaccg8auQ3kSypGIlu5XvuKxTw4y80kZ0_q8RHNQeRisSBCuitj3f6zJBJXtKYHxxVDluNnGHpwkltWogeyx0pqqp_fZlJghC4CwTzYTw1e9hVBYK-zPvxs8F_ws5y-v6E2f33TRxjszeNjN2X-AaIGTE8 |
link.rule.ids | 310,311,315,786,790,795,796,23958,23959,25170,27957,27958 |
linkProvider | Geneva Foundation for Medical Education and Research |
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=proceeding&rft.title=Peritoneal+dialysis+international&rft.atitle=MESOTHELIAL+CELLS&rft.au=YUNG%2C+Susan&rft.au=TAK+MAO+CHAN&rft.date=2007-06-01&rft.pub=Multimed&rft.issn=0896-8608&rft.volume=27&rft_id=info:doi/10.1177%2F089686080702702s19&rft.externalDBID=n%2Fa&rft.externalDocID=19942517 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0896-8608&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0896-8608&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0896-8608&client=summon |