Image analysis of remesothelialization following chemical wounding of cultured human peritoneal mesothelial cells: The role of hyaluronan synthesis

Image analysis of remesothelialization following chemical wounding of cultured human peritoneal mesothelial cells: The role of hyaluronan synthesis. To understand what happens during the wound healing process of the mesothelium, we have developed an in vitro wounding model of cultured human peritone...

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Veröffentlicht in:Kidney international 2003-12, Vol.64 (6), p.2280-2290
Hauptverfasser: Horiuchi, Takashi, Miyamoto, Keiichi, Miyamoto, Sunao, Fujita, Mika, Sano, Nami, Minamiyama, Kyoko, Fujimura, Yuichirou, Nagasawa, Koichi, Otsuka, Chie, Ohta, Yuji
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container_issue 6
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container_title Kidney international
container_volume 64
creator Horiuchi, Takashi
Miyamoto, Keiichi
Miyamoto, Sunao
Fujita, Mika
Sano, Nami
Minamiyama, Kyoko
Fujimura, Yuichirou
Nagasawa, Koichi
Otsuka, Chie
Ohta, Yuji
description Image analysis of remesothelialization following chemical wounding of cultured human peritoneal mesothelial cells: The role of hyaluronan synthesis. To understand what happens during the wound healing process of the mesothelium, we have developed an in vitro wounding model of cultured human peritoneal mesothelial cells (HPMCs) utilizing an image acquisition and analysis system. Using this system, cell mobility and hyaluronan synthesis were quantified and their interrelationship discussed. 1N NaOH was used to create circular wounds in cultured HPMC monolayers, which were then exposed for 30 minutes to the peritoneal dialysis solutions or fetal calf serum (FCS)-free M199 culture medium, followed by incubation with 0.3% FCS/M199 culture medium for up to 96hours. Digitalized microscopic date was captured every 30 minutes to quantify the wound healing process. In separate experiments, the HPMC monolayers were stained with biotin-conjugated hyaluronan-binding protein (B-HABP) at a regular time interval. Centripetal migration of the HPMCs into the wound area was the predominant process involved in wound repair with proliferation playing a secondary role. Two noticeable observations were made from the digital video movies: (1) cell mobility varied and was dependent upon the morphology and location of the cell relative to the wound edge, and (2) cell migration continued even after wound closure. Staining for B-HABP was confined to the remesothelialized area when wound closure was complete at 24hours. At 48hours after wound closure, the stained area was even more visible, although somewhat diffuse; thereafter, staining was reduced to almost background levels. The cell culture model of wound healing used in our study has enabled us to demonstrate quantitative image data of the cellular processes that occur during wound healing. We have been able to continuously observe cell migration, proliferation, and transformation. Synthesis and subsequent decomposition of hyaluronan appears to be related to the mobililty of the wounded and intact HPMCs in this model system.
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Dialysis management</topic><topic>Epithelial Cells - metabolism</topic><topic>Epithelium - growth &amp; development</topic><topic>human peritoneal mesothelial cell</topic><topic>Humans</topic><topic>hyaluronan</topic><topic>Hyaluronic Acid - biosynthesis</topic><topic>image analysis</topic><topic>Image Processing, Computer-Assisted</topic><topic>Intensive care medicine</topic><topic>Medical sciences</topic><topic>Peritoneal Diseases - chemically induced</topic><topic>Peritoneal Diseases - metabolism</topic><topic>Peritoneal Diseases - pathology</topic><topic>Peritoneal Diseases - physiopathology</topic><topic>Peritoneum - metabolism</topic><topic>Peritoneum - pathology</topic><topic>Peritoneum - physiopathology</topic><topic>Sodium Hydroxide</topic><topic>Wound Healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horiuchi, Takashi</creatorcontrib><creatorcontrib>Miyamoto, Keiichi</creatorcontrib><creatorcontrib>Miyamoto, Sunao</creatorcontrib><creatorcontrib>Fujita, Mika</creatorcontrib><creatorcontrib>Sano, Nami</creatorcontrib><creatorcontrib>Minamiyama, Kyoko</creatorcontrib><creatorcontrib>Fujimura, Yuichirou</creatorcontrib><creatorcontrib>Nagasawa, Koichi</creatorcontrib><creatorcontrib>Otsuka, Chie</creatorcontrib><creatorcontrib>Ohta, Yuji</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Kidney international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horiuchi, Takashi</au><au>Miyamoto, Keiichi</au><au>Miyamoto, Sunao</au><au>Fujita, Mika</au><au>Sano, Nami</au><au>Minamiyama, Kyoko</au><au>Fujimura, Yuichirou</au><au>Nagasawa, Koichi</au><au>Otsuka, Chie</au><au>Ohta, Yuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Image analysis of remesothelialization following chemical wounding of cultured human peritoneal mesothelial cells: The role of hyaluronan synthesis</atitle><jtitle>Kidney international</jtitle><addtitle>Kidney Int</addtitle><date>2003-12-01</date><risdate>2003</risdate><volume>64</volume><issue>6</issue><spage>2280</spage><epage>2290</epage><pages>2280-2290</pages><issn>0085-2538</issn><eissn>1523-1755</eissn><coden>KDYIA5</coden><abstract>Image analysis of remesothelialization following chemical wounding of cultured human peritoneal mesothelial cells: The role of hyaluronan synthesis. To understand what happens during the wound healing process of the mesothelium, we have developed an in vitro wounding model of cultured human peritoneal mesothelial cells (HPMCs) utilizing an image acquisition and analysis system. Using this system, cell mobility and hyaluronan synthesis were quantified and their interrelationship discussed. 1N NaOH was used to create circular wounds in cultured HPMC monolayers, which were then exposed for 30 minutes to the peritoneal dialysis solutions or fetal calf serum (FCS)-free M199 culture medium, followed by incubation with 0.3% FCS/M199 culture medium for up to 96hours. Digitalized microscopic date was captured every 30 minutes to quantify the wound healing process. In separate experiments, the HPMC monolayers were stained with biotin-conjugated hyaluronan-binding protein (B-HABP) at a regular time interval. Centripetal migration of the HPMCs into the wound area was the predominant process involved in wound repair with proliferation playing a secondary role. Two noticeable observations were made from the digital video movies: (1) cell mobility varied and was dependent upon the morphology and location of the cell relative to the wound edge, and (2) cell migration continued even after wound closure. Staining for B-HABP was confined to the remesothelialized area when wound closure was complete at 24hours. At 48hours after wound closure, the stained area was even more visible, although somewhat diffuse; thereafter, staining was reduced to almost background levels. The cell culture model of wound healing used in our study has enabled us to demonstrate quantitative image data of the cellular processes that occur during wound healing. We have been able to continuously observe cell migration, proliferation, and transformation. Synthesis and subsequent decomposition of hyaluronan appears to be related to the mobililty of the wounded and intact HPMCs in this model system.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>14633153</pmid><doi>10.1046/j.1523-1755.2003.00325.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
CAPD
Caustics
Cells, Cultured
digital video movie
Emergency and intensive care: renal failure. Dialysis management
Epithelial Cells - metabolism
Epithelium - growth & development
human peritoneal mesothelial cell
Humans
hyaluronan
Hyaluronic Acid - biosynthesis
image analysis
Image Processing, Computer-Assisted
Intensive care medicine
Medical sciences
Peritoneal Diseases - chemically induced
Peritoneal Diseases - metabolism
Peritoneal Diseases - pathology
Peritoneal Diseases - physiopathology
Peritoneum - metabolism
Peritoneum - pathology
Peritoneum - physiopathology
Sodium Hydroxide
Wound Healing
title Image analysis of remesothelialization following chemical wounding of cultured human peritoneal mesothelial cells: The role of hyaluronan synthesis
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