Cellulose-mediated mechanical property tuning in small intestinal submucosal matrix to enhance stem cell osteogenic differentiation
Natural extracellular matrices (ECM) provide a more accurate simulation of the cellular growth environment, making them excellent substrate materials for in vitro cell culture. The porcine small intestinal submucosa (SIS) is one of the most widely used natural ECM that display superior bioactivity....
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Veröffentlicht in: | International journal of biological macromolecules 2025-03, Vol.295, p.139575, Article 139575 |
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creator | Li, Boqi Gao, Yufeng Luo, Xiaohu Hu, Chuanzhi Deng, Mingyu Chen, Jinghua Gao, Min |
description | Natural extracellular matrices (ECM) provide a more accurate simulation of the cellular growth environment, making them excellent substrate materials for in vitro cell culture. The porcine small intestinal submucosa (SIS) is one of the most widely used natural ECM that display superior bioactivity. However, decellularization operations often result in fiber breakage and failure to recover mechanical strength in the SIS. In the current study, 2,3-dialdehyde cellulose (DAC) was synthesized and cross-linked with SIS gel to form hydrogels. The introduction of DAC into the SIS matrix resulted in a tunable increase in stiffness, which was instrumental in promoting stem cell adhesion and spreading, crucial factors for osteogenic differentiation. The cytotoxicity assessment confirmed the biocompatibility of the SIS-DAC hydrogels indicating their suitability for prolonged cell culture. Moreover, the degradation rate of the hydrogel could be effectively controlled by adjusting the DAC content, addressing the rapid degradation issue associated with SIS gels. This work confirmed the feasibility of using cellulose derivatives to modulate the mechanical properties of matrix gels and influence cell differentiation which offers a valuable experimental foundation for the development of advanced matrix gels tailored for cell culture and regenerative medicine applications.
2,3-Dialdehyde cellulose (DAC) was synthesized and cross-linked with porcine small intestinal submucosa (SIS) gel to form in vitro cell culture matrix. The introduction of DAC into the SIS matrix resulted in a tunable stiffness to promote stem cell osteogenic differentiation. This work presented a novel strategy for enhancing stem cell osteogenic differentiation and offered a valuable experimental foundation for the development of advanced matrix gels tailored for cell culture and regenerative medicine applications. [Display omitted] |
doi_str_mv | 10.1016/j.ijbiomac.2025.139575 |
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2,3-Dialdehyde cellulose (DAC) was synthesized and cross-linked with porcine small intestinal submucosa (SIS) gel to form in vitro cell culture matrix. The introduction of DAC into the SIS matrix resulted in a tunable stiffness to promote stem cell osteogenic differentiation. This work presented a novel strategy for enhancing stem cell osteogenic differentiation and offered a valuable experimental foundation for the development of advanced matrix gels tailored for cell culture and regenerative medicine applications. [Display omitted]</description><identifier>ISSN: 0141-8130</identifier><identifier>ISSN: 1879-0003</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2025.139575</identifier><identifier>PMID: 39788242</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Dialdehyde cellulose ; Stem cell differentiation ; Stiffness regulation</subject><ispartof>International journal of biological macromolecules, 2025-03, Vol.295, p.139575, Article 139575</ispartof><rights>2025 Elsevier B.V.</rights><rights>Copyright © 2025 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1602-67a734e37e672607c0882eded5194bc7c53559b8ad8462869b417d179983a3303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0141813025001242$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39788242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Boqi</creatorcontrib><creatorcontrib>Gao, Yufeng</creatorcontrib><creatorcontrib>Luo, Xiaohu</creatorcontrib><creatorcontrib>Hu, Chuanzhi</creatorcontrib><creatorcontrib>Deng, Mingyu</creatorcontrib><creatorcontrib>Chen, Jinghua</creatorcontrib><creatorcontrib>Gao, Min</creatorcontrib><title>Cellulose-mediated mechanical property tuning in small intestinal submucosal matrix to enhance stem cell osteogenic differentiation</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>Natural extracellular matrices (ECM) provide a more accurate simulation of the cellular growth environment, making them excellent substrate materials for in vitro cell culture. The porcine small intestinal submucosa (SIS) is one of the most widely used natural ECM that display superior bioactivity. However, decellularization operations often result in fiber breakage and failure to recover mechanical strength in the SIS. In the current study, 2,3-dialdehyde cellulose (DAC) was synthesized and cross-linked with SIS gel to form hydrogels. The introduction of DAC into the SIS matrix resulted in a tunable increase in stiffness, which was instrumental in promoting stem cell adhesion and spreading, crucial factors for osteogenic differentiation. The cytotoxicity assessment confirmed the biocompatibility of the SIS-DAC hydrogels indicating their suitability for prolonged cell culture. Moreover, the degradation rate of the hydrogel could be effectively controlled by adjusting the DAC content, addressing the rapid degradation issue associated with SIS gels. This work confirmed the feasibility of using cellulose derivatives to modulate the mechanical properties of matrix gels and influence cell differentiation which offers a valuable experimental foundation for the development of advanced matrix gels tailored for cell culture and regenerative medicine applications.
2,3-Dialdehyde cellulose (DAC) was synthesized and cross-linked with porcine small intestinal submucosa (SIS) gel to form in vitro cell culture matrix. The introduction of DAC into the SIS matrix resulted in a tunable stiffness to promote stem cell osteogenic differentiation. This work presented a novel strategy for enhancing stem cell osteogenic differentiation and offered a valuable experimental foundation for the development of advanced matrix gels tailored for cell culture and regenerative medicine applications. 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The porcine small intestinal submucosa (SIS) is one of the most widely used natural ECM that display superior bioactivity. However, decellularization operations often result in fiber breakage and failure to recover mechanical strength in the SIS. In the current study, 2,3-dialdehyde cellulose (DAC) was synthesized and cross-linked with SIS gel to form hydrogels. The introduction of DAC into the SIS matrix resulted in a tunable increase in stiffness, which was instrumental in promoting stem cell adhesion and spreading, crucial factors for osteogenic differentiation. The cytotoxicity assessment confirmed the biocompatibility of the SIS-DAC hydrogels indicating their suitability for prolonged cell culture. Moreover, the degradation rate of the hydrogel could be effectively controlled by adjusting the DAC content, addressing the rapid degradation issue associated with SIS gels. This work confirmed the feasibility of using cellulose derivatives to modulate the mechanical properties of matrix gels and influence cell differentiation which offers a valuable experimental foundation for the development of advanced matrix gels tailored for cell culture and regenerative medicine applications.
2,3-Dialdehyde cellulose (DAC) was synthesized and cross-linked with porcine small intestinal submucosa (SIS) gel to form in vitro cell culture matrix. The introduction of DAC into the SIS matrix resulted in a tunable stiffness to promote stem cell osteogenic differentiation. This work presented a novel strategy for enhancing stem cell osteogenic differentiation and offered a valuable experimental foundation for the development of advanced matrix gels tailored for cell culture and regenerative medicine applications. [Display omitted]</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39788242</pmid><doi>10.1016/j.ijbiomac.2025.139575</doi></addata></record> |
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subjects | Dialdehyde cellulose Stem cell differentiation Stiffness regulation |
title | Cellulose-mediated mechanical property tuning in small intestinal submucosal matrix to enhance stem cell osteogenic differentiation |
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