Organotypic Spheroid Culture to Mimic Radiation-Induced Salivary Hypofunction
Radiation treatment often leads to irreversible damage to normal salivary glands (SGs) because of their proximity to head and neck cancers. Optimization of the in vitro model of irradiation (IR)–induced SG damage is warranted to investigate pathophysiology and monitor treatment outcome. Here, we pre...
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Veröffentlicht in: | Journal of dental research 2017-04, Vol.96 (4), p.396-405 |
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description | Radiation treatment often leads to irreversible damage to normal salivary glands (SGs) because of their proximity to head and neck cancers. Optimization of the in vitro model of irradiation (IR)–induced SG damage is warranted to investigate pathophysiology and monitor treatment outcome. Here, we present an organotypic spheroid culture model to investigate the impact of IR on SGs and the mechanisms underlying IR-induced structural and functional changes. Human parotid epithelial cells were obtained from human parotid glands and plated on either plastic plates or Matrigel. A number of 3-dimensional (3D) spheroids were assembled on Matrigel. After IR at 10 and 20 Gy, morphologic changes in cells in 2D monolayers and 3D spheroids were observed. As the structural integrity of the 3D spheroids was destroyed by IR, the expression levels of salivary epithelial and structural proteins and genes decreased proportionally with radiation dosage. Furthermore, the spheroid culture allowed better measurement of functional alterations following IR relative to the monolayer culture, in which IR-inflicted spheroids exhibited a loss of acinar-specific cellular functions that enable Ca2+ influx or secretion of α-amylase in response to cholinergic or β-adrenergic agonists. p53-mediated apoptotic cell death was observed under both culture conditions, and its downstream signals increased, such as p53 upregulated modulator of apoptosis (PUMA), Bax, cytochrome c, caspase 9, and caspase 3. These results suggest that the organotypic spheroid culture could provide a useful alternative model for exploration of radiobiology and mode of action of new therapies for prevention of radiation-induced salivary hypofunction. |
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Optimization of the in vitro model of irradiation (IR)–induced SG damage is warranted to investigate pathophysiology and monitor treatment outcome. Here, we present an organotypic spheroid culture model to investigate the impact of IR on SGs and the mechanisms underlying IR-induced structural and functional changes. Human parotid epithelial cells were obtained from human parotid glands and plated on either plastic plates or Matrigel. A number of 3-dimensional (3D) spheroids were assembled on Matrigel. After IR at 10 and 20 Gy, morphologic changes in cells in 2D monolayers and 3D spheroids were observed. As the structural integrity of the 3D spheroids was destroyed by IR, the expression levels of salivary epithelial and structural proteins and genes decreased proportionally with radiation dosage. Furthermore, the spheroid culture allowed better measurement of functional alterations following IR relative to the monolayer culture, in which IR-inflicted spheroids exhibited a loss of acinar-specific cellular functions that enable Ca2+ influx or secretion of α-amylase in response to cholinergic or β-adrenergic agonists. p53-mediated apoptotic cell death was observed under both culture conditions, and its downstream signals increased, such as p53 upregulated modulator of apoptosis (PUMA), Bax, cytochrome c, caspase 9, and caspase 3. These results suggest that the organotypic spheroid culture could provide a useful alternative model for exploration of radiobiology and mode of action of new therapies for prevention of radiation-induced salivary hypofunction.</description><identifier>ISSN: 0022-0345</identifier><identifier>EISSN: 1544-0591</identifier><identifier>DOI: 10.1177/0022034516685036</identifier><identifier>PMID: 28048945</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Adult ; Aged ; Apoptosis ; Bax protein ; Blotting, Western ; Calcium influx ; Caspase ; Caspase-3 ; Caspase-9 ; Cell culture ; Cell Culture Techniques - methods ; Cell cycle ; Cell death ; Cell Survival ; Cytochrome ; Cytochrome c ; Dentistry ; Drug dosages ; Epithelial cells ; Epithelial Cells - radiation effects ; Fluorescent Antibody Technique ; Gene expression ; Head and neck ; Head and Neck Neoplasms - radiotherapy ; Humans ; I.R. radiation ; In Situ Nick-End Labeling ; Investigations ; Male ; Medical laboratories ; Middle Aged ; Morphology ; p53 Protein ; Parotid Gland - cytology ; Proteins ; Radiation Dosage ; Radiation therapy ; Real-Time Polymerase Chain Reaction ; Salivary gland ; Salivary Glands - radiation effects ; Secretion ; Signal transduction ; Spheroids ; Statistical analysis ; Structural proteins ; Structure-function relationships ; Sympathomimetics ; Tissue Engineering - methods ; Variance analysis ; α-Amylase</subject><ispartof>Journal of dental research, 2017-04, Vol.96 (4), p.396-405</ispartof><rights>International & American Associations for Dental Research 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-bfee1faee39447d86ac128dbff0bba9895db19c5b9ed1da35bbb040a18d8bd13</citedby><cites>FETCH-LOGICAL-c365t-bfee1faee39447d86ac128dbff0bba9895db19c5b9ed1da35bbb040a18d8bd13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0022034516685036$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0022034516685036$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,777,781,21800,27905,27906,43602,43603</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28048945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shin, H.S.</creatorcontrib><creatorcontrib>An, H.Y</creatorcontrib><creatorcontrib>Choi, J.S.</creatorcontrib><creatorcontrib>Kim, H.J.</creatorcontrib><creatorcontrib>Lim, J.Y.</creatorcontrib><title>Organotypic Spheroid Culture to Mimic Radiation-Induced Salivary Hypofunction</title><title>Journal of dental research</title><addtitle>J Dent Res</addtitle><description>Radiation treatment often leads to irreversible damage to normal salivary glands (SGs) because of their proximity to head and neck cancers. Optimization of the in vitro model of irradiation (IR)–induced SG damage is warranted to investigate pathophysiology and monitor treatment outcome. Here, we present an organotypic spheroid culture model to investigate the impact of IR on SGs and the mechanisms underlying IR-induced structural and functional changes. Human parotid epithelial cells were obtained from human parotid glands and plated on either plastic plates or Matrigel. A number of 3-dimensional (3D) spheroids were assembled on Matrigel. After IR at 10 and 20 Gy, morphologic changes in cells in 2D monolayers and 3D spheroids were observed. As the structural integrity of the 3D spheroids was destroyed by IR, the expression levels of salivary epithelial and structural proteins and genes decreased proportionally with radiation dosage. Furthermore, the spheroid culture allowed better measurement of functional alterations following IR relative to the monolayer culture, in which IR-inflicted spheroids exhibited a loss of acinar-specific cellular functions that enable Ca2+ influx or secretion of α-amylase in response to cholinergic or β-adrenergic agonists. p53-mediated apoptotic cell death was observed under both culture conditions, and its downstream signals increased, such as p53 upregulated modulator of apoptosis (PUMA), Bax, cytochrome c, caspase 9, and caspase 3. These results suggest that the organotypic spheroid culture could provide a useful alternative model for exploration of radiobiology and mode of action of new therapies for prevention of radiation-induced salivary hypofunction.</description><subject>Adult</subject><subject>Aged</subject><subject>Apoptosis</subject><subject>Bax protein</subject><subject>Blotting, Western</subject><subject>Calcium influx</subject><subject>Caspase</subject><subject>Caspase-3</subject><subject>Caspase-9</subject><subject>Cell culture</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell cycle</subject><subject>Cell death</subject><subject>Cell Survival</subject><subject>Cytochrome</subject><subject>Cytochrome c</subject><subject>Dentistry</subject><subject>Drug dosages</subject><subject>Epithelial cells</subject><subject>Epithelial Cells - radiation effects</subject><subject>Fluorescent Antibody Technique</subject><subject>Gene expression</subject><subject>Head and neck</subject><subject>Head and Neck Neoplasms - radiotherapy</subject><subject>Humans</subject><subject>I.R. radiation</subject><subject>In Situ Nick-End Labeling</subject><subject>Investigations</subject><subject>Male</subject><subject>Medical laboratories</subject><subject>Middle Aged</subject><subject>Morphology</subject><subject>p53 Protein</subject><subject>Parotid Gland - cytology</subject><subject>Proteins</subject><subject>Radiation Dosage</subject><subject>Radiation therapy</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Salivary gland</subject><subject>Salivary Glands - radiation effects</subject><subject>Secretion</subject><subject>Signal transduction</subject><subject>Spheroids</subject><subject>Statistical analysis</subject><subject>Structural proteins</subject><subject>Structure-function relationships</subject><subject>Sympathomimetics</subject><subject>Tissue Engineering - methods</subject><subject>Variance analysis</subject><subject>α-Amylase</subject><issn>0022-0345</issn><issn>1544-0591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1Lw0AQxRdRbK3ePUnAi5fo7G422RylqC20FGzvYb9SU5Js3E2E_vcmtCoUPM3h_d6bmYfQLYZHjJPkCYAQoBHDccwZ0PgMjTGLohBYis_ReJDDQR-hK-93ADglnF6iEeEQ8TRiY7Rcua2obbtvChWsmw_jbKGDaVe2nTNBa4NlUfXKu9CFaAtbh_Nad8roYC3K4ku4fTDbNzbvajWo1-giF6U3N8c5QZvXl810Fi5Wb_Pp8yJUNGZtKHNjcC6MoWkUJZrHQmHCtcxzkFKkPGVa4lQxmRqNtaBMSgkRCMw1lxrTCXo4xDbOfnbGt1lVeGXKUtTGdj7DnDFKCUmSHr0_QXe2c3V_XEYoAOMx8IGCA6Wc9d6ZPGtcUfXfZRiyoenstOnecncM7mRl9K_hp9oeCA-AF1vzt_XfwG8VpIYv</recordid><startdate>201704</startdate><enddate>201704</enddate><creator>Shin, H.S.</creator><creator>An, H.Y</creator><creator>Choi, J.S.</creator><creator>Kim, H.J.</creator><creator>Lim, J.Y.</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>201704</creationdate><title>Organotypic Spheroid Culture to Mimic Radiation-Induced Salivary Hypofunction</title><author>Shin, H.S. ; An, H.Y ; Choi, J.S. ; Kim, H.J. ; Lim, J.Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-bfee1faee39447d86ac128dbff0bba9895db19c5b9ed1da35bbb040a18d8bd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Apoptosis</topic><topic>Bax protein</topic><topic>Blotting, Western</topic><topic>Calcium influx</topic><topic>Caspase</topic><topic>Caspase-3</topic><topic>Caspase-9</topic><topic>Cell culture</topic><topic>Cell Culture Techniques - methods</topic><topic>Cell cycle</topic><topic>Cell death</topic><topic>Cell Survival</topic><topic>Cytochrome</topic><topic>Cytochrome c</topic><topic>Dentistry</topic><topic>Drug dosages</topic><topic>Epithelial cells</topic><topic>Epithelial Cells - radiation effects</topic><topic>Fluorescent Antibody Technique</topic><topic>Gene expression</topic><topic>Head and neck</topic><topic>Head and Neck Neoplasms - radiotherapy</topic><topic>Humans</topic><topic>I.R. radiation</topic><topic>In Situ Nick-End Labeling</topic><topic>Investigations</topic><topic>Male</topic><topic>Medical laboratories</topic><topic>Middle Aged</topic><topic>Morphology</topic><topic>p53 Protein</topic><topic>Parotid Gland - cytology</topic><topic>Proteins</topic><topic>Radiation Dosage</topic><topic>Radiation therapy</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Salivary gland</topic><topic>Salivary Glands - radiation effects</topic><topic>Secretion</topic><topic>Signal transduction</topic><topic>Spheroids</topic><topic>Statistical analysis</topic><topic>Structural proteins</topic><topic>Structure-function relationships</topic><topic>Sympathomimetics</topic><topic>Tissue Engineering - methods</topic><topic>Variance analysis</topic><topic>α-Amylase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shin, H.S.</creatorcontrib><creatorcontrib>An, H.Y</creatorcontrib><creatorcontrib>Choi, J.S.</creatorcontrib><creatorcontrib>Kim, H.J.</creatorcontrib><creatorcontrib>Lim, J.Y.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dental research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shin, H.S.</au><au>An, H.Y</au><au>Choi, J.S.</au><au>Kim, H.J.</au><au>Lim, J.Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Organotypic Spheroid Culture to Mimic Radiation-Induced Salivary Hypofunction</atitle><jtitle>Journal of dental research</jtitle><addtitle>J Dent Res</addtitle><date>2017-04</date><risdate>2017</risdate><volume>96</volume><issue>4</issue><spage>396</spage><epage>405</epage><pages>396-405</pages><issn>0022-0345</issn><eissn>1544-0591</eissn><abstract>Radiation treatment often leads to irreversible damage to normal salivary glands (SGs) because of their proximity to head and neck cancers. Optimization of the in vitro model of irradiation (IR)–induced SG damage is warranted to investigate pathophysiology and monitor treatment outcome. Here, we present an organotypic spheroid culture model to investigate the impact of IR on SGs and the mechanisms underlying IR-induced structural and functional changes. Human parotid epithelial cells were obtained from human parotid glands and plated on either plastic plates or Matrigel. A number of 3-dimensional (3D) spheroids were assembled on Matrigel. After IR at 10 and 20 Gy, morphologic changes in cells in 2D monolayers and 3D spheroids were observed. As the structural integrity of the 3D spheroids was destroyed by IR, the expression levels of salivary epithelial and structural proteins and genes decreased proportionally with radiation dosage. Furthermore, the spheroid culture allowed better measurement of functional alterations following IR relative to the monolayer culture, in which IR-inflicted spheroids exhibited a loss of acinar-specific cellular functions that enable Ca2+ influx or secretion of α-amylase in response to cholinergic or β-adrenergic agonists. p53-mediated apoptotic cell death was observed under both culture conditions, and its downstream signals increased, such as p53 upregulated modulator of apoptosis (PUMA), Bax, cytochrome c, caspase 9, and caspase 3. These results suggest that the organotypic spheroid culture could provide a useful alternative model for exploration of radiobiology and mode of action of new therapies for prevention of radiation-induced salivary hypofunction.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>28048945</pmid><doi>10.1177/0022034516685036</doi><tpages>10</tpages></addata></record> |
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subjects | Adult Aged Apoptosis Bax protein Blotting, Western Calcium influx Caspase Caspase-3 Caspase-9 Cell culture Cell Culture Techniques - methods Cell cycle Cell death Cell Survival Cytochrome Cytochrome c Dentistry Drug dosages Epithelial cells Epithelial Cells - radiation effects Fluorescent Antibody Technique Gene expression Head and neck Head and Neck Neoplasms - radiotherapy Humans I.R. radiation In Situ Nick-End Labeling Investigations Male Medical laboratories Middle Aged Morphology p53 Protein Parotid Gland - cytology Proteins Radiation Dosage Radiation therapy Real-Time Polymerase Chain Reaction Salivary gland Salivary Glands - radiation effects Secretion Signal transduction Spheroids Statistical analysis Structural proteins Structure-function relationships Sympathomimetics Tissue Engineering - methods Variance analysis α-Amylase |
title | Organotypic Spheroid Culture to Mimic Radiation-Induced Salivary Hypofunction |
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