Corneal epithelial-stromal constructs to study differences associated with diabetes mellitus
Diabetes mellitus (DM) is a common metabolic disease associated with severe macrovascular and microvascular complications that influence nearly every tissue in the body, including the anterior and posterior segments of the eye. In the cornea, DM is associated with recurrent epithelial erosion and re...
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Veröffentlicht in: | Experimental eye research 2024-11, Vol.248, p.110100, Article 110100 |
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description | Diabetes mellitus (DM) is a common metabolic disease associated with severe macrovascular and microvascular complications that influence nearly every tissue in the body, including the anterior and posterior segments of the eye. In the cornea, DM is associated with recurrent epithelial erosion and reduced wound-healing capacity, which increases the risk of corneal scarring. We previously developed a co-culture model of the cornea consisting of immortalized human corneal epithelial cells (hCE-TJ) overlaying a self-assembled stromal layer generated by human corneal fibroblasts (hCFs) over a 4-week period. In this study, we investigated epithelial-stromal constructs generated from hCFs derived from subjects with Type 1 (T1DM) or 2 diabetes (T2DM) compared to controls. We found that T2DM constructs exhibited a disrupted epithelium and a thicker, stratified stromal layer compared to controls or T1DM. Both T1DM and T2DM stromal constructs expressed lower expression of thrombospondin-1 in isolated extracellular vesicles (EVs) compared to controls with no significant difference observed in the presence of epithelial cells, suggesting that reduced provisional matrix secretion in the corneal stroma may be a factor that promotes delayed corneal wound healing in diabetes. The tetraspanins are established extracellular vesicle (EV) markers and include CD63, CD81, and CD9, and were highly expressed by EVs in all three cell types. Control corneal stromal fibroblasts produced more and larger EVs when compared to T1DM and T2DM hCF-derived EVs, supporting a role for altered cell-cell communication in the context of DM. Further characterization of EVs and their cargo is expected to aid in the development of targeted treatments to improve corneal wound healing.
•Type 2 diabetic constructs were thicker with epithelial defects compared to Healthy.•Reduced thrombospondin-1 in extracellular vesicles secreted from DM constructs.•All three tetraspanins were highly expressed in EVs from Healthy, T1DM and T2DM.•EVs derived from healthy constructs had larger sizes and more total particles. |
doi_str_mv | 10.1016/j.exer.2024.110100 |
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•Type 2 diabetic constructs were thicker with epithelial defects compared to Healthy.•Reduced thrombospondin-1 in extracellular vesicles secreted from DM constructs.•All three tetraspanins were highly expressed in EVs from Healthy, T1DM and T2DM.•EVs derived from healthy constructs had larger sizes and more total particles.</description><identifier>ISSN: 0014-4835</identifier><identifier>ISSN: 1096-0007</identifier><identifier>EISSN: 1096-0007</identifier><identifier>DOI: 10.1016/j.exer.2024.110100</identifier><identifier>PMID: 39299675</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Cells, Cultured ; Coculture Techniques ; Corneal Stroma - metabolism ; Corneal Stroma - pathology ; Diabetes Mellitus, Type 1 - complications ; Diabetes Mellitus, Type 1 - metabolism ; Diabetes Mellitus, Type 1 - pathology ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - metabolism ; Diabetic neuropathy ; Endosomal ; Epithelium, Corneal - metabolism ; Epithelium, Corneal - pathology ; Exosomes ; Extracellular vesicles ; Fibroblasts - metabolism ; Fibroblasts - pathology ; Humans ; Keratectomy ; Male ; Thrombospondin 1 - metabolism ; Tissue-engineered cornea ; Wound Healing - physiology</subject><ispartof>Experimental eye research, 2024-11, Vol.248, p.110100, Article 110100</ispartof><rights>2024 Elsevier Ltd</rights><rights>Copyright © 2024 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c237t-fd1da1d5db5c58b01e3a851817e114715928fd60be3efdedbaf47e9cc9dcf3083</cites><orcidid>0000-0002-8761-3824</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014483524003221$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39299675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hefley, Brenna S.</creatorcontrib><creatorcontrib>McKay, Tina B.</creatorcontrib><creatorcontrib>Hutcheon, Audrey E.K.</creatorcontrib><creatorcontrib>Ciolino, Joseph B.</creatorcontrib><creatorcontrib>Karamichos, Dimitrios</creatorcontrib><title>Corneal epithelial-stromal constructs to study differences associated with diabetes mellitus</title><title>Experimental eye research</title><addtitle>Exp Eye Res</addtitle><description>Diabetes mellitus (DM) is a common metabolic disease associated with severe macrovascular and microvascular complications that influence nearly every tissue in the body, including the anterior and posterior segments of the eye. In the cornea, DM is associated with recurrent epithelial erosion and reduced wound-healing capacity, which increases the risk of corneal scarring. We previously developed a co-culture model of the cornea consisting of immortalized human corneal epithelial cells (hCE-TJ) overlaying a self-assembled stromal layer generated by human corneal fibroblasts (hCFs) over a 4-week period. In this study, we investigated epithelial-stromal constructs generated from hCFs derived from subjects with Type 1 (T1DM) or 2 diabetes (T2DM) compared to controls. We found that T2DM constructs exhibited a disrupted epithelium and a thicker, stratified stromal layer compared to controls or T1DM. Both T1DM and T2DM stromal constructs expressed lower expression of thrombospondin-1 in isolated extracellular vesicles (EVs) compared to controls with no significant difference observed in the presence of epithelial cells, suggesting that reduced provisional matrix secretion in the corneal stroma may be a factor that promotes delayed corneal wound healing in diabetes. The tetraspanins are established extracellular vesicle (EV) markers and include CD63, CD81, and CD9, and were highly expressed by EVs in all three cell types. Control corneal stromal fibroblasts produced more and larger EVs when compared to T1DM and T2DM hCF-derived EVs, supporting a role for altered cell-cell communication in the context of DM. Further characterization of EVs and their cargo is expected to aid in the development of targeted treatments to improve corneal wound healing.
•Type 2 diabetic constructs were thicker with epithelial defects compared to Healthy.•Reduced thrombospondin-1 in extracellular vesicles secreted from DM constructs.•All three tetraspanins were highly expressed in EVs from Healthy, T1DM and T2DM.•EVs derived from healthy constructs had larger sizes and more total particles.</description><subject>Cells, Cultured</subject><subject>Coculture Techniques</subject><subject>Corneal Stroma - metabolism</subject><subject>Corneal Stroma - pathology</subject><subject>Diabetes Mellitus, Type 1 - complications</subject><subject>Diabetes Mellitus, Type 1 - metabolism</subject><subject>Diabetes Mellitus, Type 1 - pathology</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Diabetic neuropathy</subject><subject>Endosomal</subject><subject>Epithelium, Corneal - metabolism</subject><subject>Epithelium, Corneal - pathology</subject><subject>Exosomes</subject><subject>Extracellular vesicles</subject><subject>Fibroblasts - metabolism</subject><subject>Fibroblasts - pathology</subject><subject>Humans</subject><subject>Keratectomy</subject><subject>Male</subject><subject>Thrombospondin 1 - metabolism</subject><subject>Tissue-engineered cornea</subject><subject>Wound Healing - physiology</subject><issn>0014-4835</issn><issn>1096-0007</issn><issn>1096-0007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxDAUhYMozjj6B1xIl25ak6bpA9zI4AsG3OhOCGlygxnaZkxSdf69KVWXru7l3HMOyYfQOcEZwaS82mbwBS7LcV5kJCoYH6AlwU2ZYoyrQ7TEmBRpUVO2QCfeb6NKi6o4Rgva5E1TVmyJXtfWDSC6BHYmvEFnRJf64GwfJWmHuI4y-CTYxIdR7RNltAYHgwSfCO-tNCKASj5jON5ECyEeeug6E0Z_io606Dyc_cwVerm7fV4_pJun-8f1zSaVOa1CqhVRgiimWiZZ3WICVNSM1KQCQoqKsCavtSpxCxS0AtUKXVTQSNkoqSmu6Qpdzr07Z99H8IH3xsv4CDGAHT2nBMeWOq9ZtOazVTrrvQPNd870wu05wXyiyrd8osonqnymGkMXP_1j24P6i_xijIbr2QDxlx8mxr00EyRlHMjAlTX_9X8DjLyLSA</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Hefley, Brenna S.</creator><creator>McKay, Tina B.</creator><creator>Hutcheon, Audrey E.K.</creator><creator>Ciolino, Joseph B.</creator><creator>Karamichos, Dimitrios</creator><general>Elsevier Ltd</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>7X8</scope><orcidid>https://orcid.org/0000-0002-8761-3824</orcidid></search><sort><creationdate>202411</creationdate><title>Corneal epithelial-stromal constructs to study differences associated with diabetes mellitus</title><author>Hefley, Brenna S. ; McKay, Tina B. ; Hutcheon, Audrey E.K. ; Ciolino, Joseph B. ; Karamichos, Dimitrios</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c237t-fd1da1d5db5c58b01e3a851817e114715928fd60be3efdedbaf47e9cc9dcf3083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Cells, Cultured</topic><topic>Coculture Techniques</topic><topic>Corneal Stroma - metabolism</topic><topic>Corneal Stroma - pathology</topic><topic>Diabetes Mellitus, Type 1 - complications</topic><topic>Diabetes Mellitus, Type 1 - metabolism</topic><topic>Diabetes Mellitus, Type 1 - pathology</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Diabetic neuropathy</topic><topic>Endosomal</topic><topic>Epithelium, Corneal - metabolism</topic><topic>Epithelium, Corneal - pathology</topic><topic>Exosomes</topic><topic>Extracellular vesicles</topic><topic>Fibroblasts - metabolism</topic><topic>Fibroblasts - pathology</topic><topic>Humans</topic><topic>Keratectomy</topic><topic>Male</topic><topic>Thrombospondin 1 - metabolism</topic><topic>Tissue-engineered cornea</topic><topic>Wound Healing - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hefley, Brenna S.</creatorcontrib><creatorcontrib>McKay, Tina B.</creatorcontrib><creatorcontrib>Hutcheon, Audrey E.K.</creatorcontrib><creatorcontrib>Ciolino, Joseph B.</creatorcontrib><creatorcontrib>Karamichos, Dimitrios</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hefley, Brenna S.</au><au>McKay, Tina B.</au><au>Hutcheon, Audrey E.K.</au><au>Ciolino, Joseph B.</au><au>Karamichos, Dimitrios</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corneal epithelial-stromal constructs to study differences associated with diabetes mellitus</atitle><jtitle>Experimental eye research</jtitle><addtitle>Exp Eye Res</addtitle><date>2024-11</date><risdate>2024</risdate><volume>248</volume><spage>110100</spage><pages>110100-</pages><artnum>110100</artnum><issn>0014-4835</issn><issn>1096-0007</issn><eissn>1096-0007</eissn><abstract>Diabetes mellitus (DM) is a common metabolic disease associated with severe macrovascular and microvascular complications that influence nearly every tissue in the body, including the anterior and posterior segments of the eye. In the cornea, DM is associated with recurrent epithelial erosion and reduced wound-healing capacity, which increases the risk of corneal scarring. We previously developed a co-culture model of the cornea consisting of immortalized human corneal epithelial cells (hCE-TJ) overlaying a self-assembled stromal layer generated by human corneal fibroblasts (hCFs) over a 4-week period. In this study, we investigated epithelial-stromal constructs generated from hCFs derived from subjects with Type 1 (T1DM) or 2 diabetes (T2DM) compared to controls. We found that T2DM constructs exhibited a disrupted epithelium and a thicker, stratified stromal layer compared to controls or T1DM. Both T1DM and T2DM stromal constructs expressed lower expression of thrombospondin-1 in isolated extracellular vesicles (EVs) compared to controls with no significant difference observed in the presence of epithelial cells, suggesting that reduced provisional matrix secretion in the corneal stroma may be a factor that promotes delayed corneal wound healing in diabetes. The tetraspanins are established extracellular vesicle (EV) markers and include CD63, CD81, and CD9, and were highly expressed by EVs in all three cell types. Control corneal stromal fibroblasts produced more and larger EVs when compared to T1DM and T2DM hCF-derived EVs, supporting a role for altered cell-cell communication in the context of DM. Further characterization of EVs and their cargo is expected to aid in the development of targeted treatments to improve corneal wound healing.
•Type 2 diabetic constructs were thicker with epithelial defects compared to Healthy.•Reduced thrombospondin-1 in extracellular vesicles secreted from DM constructs.•All three tetraspanins were highly expressed in EVs from Healthy, T1DM and T2DM.•EVs derived from healthy constructs had larger sizes and more total particles.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>39299675</pmid><doi>10.1016/j.exer.2024.110100</doi><orcidid>https://orcid.org/0000-0002-8761-3824</orcidid></addata></record> |
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subjects | Cells, Cultured Coculture Techniques Corneal Stroma - metabolism Corneal Stroma - pathology Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - metabolism Diabetes Mellitus, Type 1 - pathology Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - metabolism Diabetic neuropathy Endosomal Epithelium, Corneal - metabolism Epithelium, Corneal - pathology Exosomes Extracellular vesicles Fibroblasts - metabolism Fibroblasts - pathology Humans Keratectomy Male Thrombospondin 1 - metabolism Tissue-engineered cornea Wound Healing - physiology |
title | Corneal epithelial-stromal constructs to study differences associated with diabetes mellitus |
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