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Dynamic observation and quantification of type I/II collagen in chondrogenesis of mesenchymal stem cells by second‐order susceptibility microscopy
Second‐order susceptibility (SOS) microscopy is used to image and characterize chondrogenesis in cultured human mesenchymal stem cells. SOS analysis shows that the SOS tensor ratios can be used to characterize type I and II collagens in living tissues and that both collagen types are produced at the...
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Published in: | Journal of biophotonics 2019-02, Vol.12 (2), p.e201800097-n/a |
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description | Second‐order susceptibility (SOS) microscopy is used to image and characterize chondrogenesis in cultured human mesenchymal stem cells. SOS analysis shows that the SOS tensor ratios can be used to characterize type I and II collagens in living tissues and that both collagen types are produced at the onset of chondrogenesis. Time‐lapse analysis shows a modulation of extracellular matrix results in a higher rate in increase of type II collagen, as compared to type I collagen. With time, type II collagen content stabilizes at the composition of 70% of total collagen content. SOS microscopy can be used to continuously and noninvasively monitor the production of collagens I and II. With additional development, this technique can be developed into an effective quality control tool for monitoring extracellular matrix production in engineered tissues.
Second‐order susceptibility (SOS) microscopy is used to image and characterize chondrogenesis in cultured human mesenchymal stem cells. Without extrinsic labeling, SOS tensor ratios analysis can be used to quantify the production of type I/II collagens continuously and noninvasively in living tissues. This technique can be developed into an effective quality control tool for monitoring extracellular matrix production in engineered tissues. |
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Second‐order susceptibility (SOS) microscopy is used to image and characterize chondrogenesis in cultured human mesenchymal stem cells. Without extrinsic labeling, SOS tensor ratios analysis can be used to quantify the production of type I/II collagens continuously and noninvasively in living tissues. This technique can be developed into an effective quality control tool for monitoring extracellular matrix production in engineered tissues.</description><identifier>ISSN: 1864-063X</identifier><identifier>EISSN: 1864-0648</identifier><identifier>DOI: 10.1002/jbio.201800097</identifier><identifier>PMID: 29920965</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag GmbH & Co. KGaA</publisher><subject>Chondrogenesis ; Collagen ; Collagen (type I) ; Collagen (type II) ; Collagen Type I - metabolism ; Collagen Type II - metabolism ; differentiation ; Extracellular matrix ; Humans ; Mesenchymal stem cells ; Mesenchymal Stem Cells - cytology ; Mesenchymal Stem Cells - metabolism ; Mesenchyme ; Microscopy ; Quality control ; second‐order susceptibility microscopy ; Stem cells ; Tensors ; Tissue engineering ; Tissues</subject><ispartof>Journal of biophotonics, 2019-02, Vol.12 (2), p.e201800097-n/a</ispartof><rights>2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3287-2af75e74fd24262a8cf81dd749031106c8a5081da3adc9c21ed2fdac11fc0afd3</cites><orcidid>0000-0002-3690-9342</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29920965$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hsueh, Chiu‐Mei</creatorcontrib><creatorcontrib>Lin, Hung‐Ming</creatorcontrib><creatorcontrib>Tseng, Te‐Yu</creatorcontrib><creatorcontrib>Huang, Yao‐De</creatorcontrib><creatorcontrib>Lee, Hsuan‐Shu</creatorcontrib><creatorcontrib>Dong, Chen‐Yuan</creatorcontrib><title>Dynamic observation and quantification of type I/II collagen in chondrogenesis of mesenchymal stem cells by second‐order susceptibility microscopy</title><title>Journal of biophotonics</title><addtitle>J Biophotonics</addtitle><description>Second‐order susceptibility (SOS) microscopy is used to image and characterize chondrogenesis in cultured human mesenchymal stem cells. SOS analysis shows that the SOS tensor ratios can be used to characterize type I and II collagens in living tissues and that both collagen types are produced at the onset of chondrogenesis. Time‐lapse analysis shows a modulation of extracellular matrix results in a higher rate in increase of type II collagen, as compared to type I collagen. With time, type II collagen content stabilizes at the composition of 70% of total collagen content. SOS microscopy can be used to continuously and noninvasively monitor the production of collagens I and II. With additional development, this technique can be developed into an effective quality control tool for monitoring extracellular matrix production in engineered tissues.
Second‐order susceptibility (SOS) microscopy is used to image and characterize chondrogenesis in cultured human mesenchymal stem cells. Without extrinsic labeling, SOS tensor ratios analysis can be used to quantify the production of type I/II collagens continuously and noninvasively in living tissues. This technique can be developed into an effective quality control tool for monitoring extracellular matrix production in engineered tissues.</description><subject>Chondrogenesis</subject><subject>Collagen</subject><subject>Collagen (type I)</subject><subject>Collagen (type II)</subject><subject>Collagen Type I - metabolism</subject><subject>Collagen Type II - metabolism</subject><subject>differentiation</subject><subject>Extracellular matrix</subject><subject>Humans</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchymal Stem Cells - cytology</subject><subject>Mesenchymal Stem Cells - metabolism</subject><subject>Mesenchyme</subject><subject>Microscopy</subject><subject>Quality control</subject><subject>second‐order susceptibility microscopy</subject><subject>Stem cells</subject><subject>Tensors</subject><subject>Tissue engineering</subject><subject>Tissues</subject><issn>1864-063X</issn><issn>1864-0648</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkb9u1TAUxi1ERUthZUSWWFjure04cTJCKZCqUheQ2CzHPqa-SuzUTkDZ-ggMPCFPgqPbXqQuTOePfufTd_Qh9IqSLSWEne06F7aM0JoQ0ogn6ITWFd-QitdPD33x7Rg9T2lHSEWKsniGjlnTMNJU5Qn6_WHxanAahy5B_KEmFzxW3uDbWfnJWaf3q2DxtIyA27O2xTr0vfoOHjuP9U3wJoY8QXJp5QZI4PXNMqgepwkGrKHvE-4WnEBn-M_drxANRJzmpGGcXOd6Ny04u4gh6TAuL9CRVX2Cl_f1FH39ePHl_PPm6vpTe_7uaqMLVosNU1aUILg1jLOKqVrbmhojeEMKSkmla1WSvFGFMrrRjIJh1ihNqdVEWVOcord73TGG2xnSJAeXVrfKQ5iTZKQUnPOyEBl98wjdhTn67E4yKhoqhGh4prZ7av0kRbByjG5QcZGUyDUvueYlD3nlg9f3snM3gDngDwFloNkDP10Py3_k5OX79vqf-F8Pvqa1</recordid><startdate>201902</startdate><enddate>201902</enddate><creator>Hsueh, Chiu‐Mei</creator><creator>Lin, Hung‐Ming</creator><creator>Tseng, Te‐Yu</creator><creator>Huang, Yao‐De</creator><creator>Lee, Hsuan‐Shu</creator><creator>Dong, Chen‐Yuan</creator><general>WILEY‐VCH Verlag GmbH & Co. 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SOS analysis shows that the SOS tensor ratios can be used to characterize type I and II collagens in living tissues and that both collagen types are produced at the onset of chondrogenesis. Time‐lapse analysis shows a modulation of extracellular matrix results in a higher rate in increase of type II collagen, as compared to type I collagen. With time, type II collagen content stabilizes at the composition of 70% of total collagen content. SOS microscopy can be used to continuously and noninvasively monitor the production of collagens I and II. With additional development, this technique can be developed into an effective quality control tool for monitoring extracellular matrix production in engineered tissues.
Second‐order susceptibility (SOS) microscopy is used to image and characterize chondrogenesis in cultured human mesenchymal stem cells. Without extrinsic labeling, SOS tensor ratios analysis can be used to quantify the production of type I/II collagens continuously and noninvasively in living tissues. This technique can be developed into an effective quality control tool for monitoring extracellular matrix production in engineered tissues.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH & Co. KGaA</pub><pmid>29920965</pmid><doi>10.1002/jbio.201800097</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3690-9342</orcidid></addata></record> |
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subjects | Chondrogenesis Collagen Collagen (type I) Collagen (type II) Collagen Type I - metabolism Collagen Type II - metabolism differentiation Extracellular matrix Humans Mesenchymal stem cells Mesenchymal Stem Cells - cytology Mesenchymal Stem Cells - metabolism Mesenchyme Microscopy Quality control second‐order susceptibility microscopy Stem cells Tensors Tissue engineering Tissues |
title | Dynamic observation and quantification of type I/II collagen in chondrogenesis of mesenchymal stem cells by second‐order susceptibility microscopy |
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