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Calcium-responsible injectable peptide hydrogel encapsulating BMSCs for promoting femur regeneration
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作者 Xia Wu tingfen deng +7 位作者 Wenbing Liu Hong Han Wei Xie Wenjie Wang Dan Yuan Lisha Zha Junfeng Shi Xiaoyun Pan 《Science China Chemistry》 2025年第6期2595-2604,共10页
Effectively managing bone defects presents significant clinical challenges,where bone marrow mesenchymal stem cells(BMSCs)offer promising potential for bone regeneration.However,delivering BMSCs effectively requires s... Effectively managing bone defects presents significant clinical challenges,where bone marrow mesenchymal stem cells(BMSCs)offer promising potential for bone regeneration.However,delivering BMSCs effectively requires suitable biomaterials.Herein,we introduce,Pep1,a calcium-responsive peptide designed for delivering BMSCs for femur regeneration.Pep1self-assembles to form a pericellular hydrogel in the presence of calcium ions,forming a nanofiber-rich network conductive to BMSCs encapsulation.Important,Pep1 hydrogel supports BMSC activity in 3D cell culture without compromise.In vitro and in vivo studies demonstrate excellent biocompatibility of Pep1 hydrogel.Osteogenic differentiation and q-PCR assays reveal that Pep1 enhances osteogenic differentiation and upregulates bone-related genes expression.Furthermore,In vivo experiments confirm that Pep1 hydrogel encapsulating BMSCs significantly improves femur defect repair.This study underscores Pep1 as a promising biomaterial for calcium-responsive bone tissue regeneration. 展开更多
关键词 pericellular peptide hydrogel self-assembly BMSC encapsulation osteogenic differentiation femur defects repair
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Predictive value of T cell receptor repertoire profiling for immunosuppressive therapy in severe aplastic anemia 被引量:1
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作者 Cunte Chen Yuling Zhang +16 位作者 Dongpei Lu Zelong Zhang Jun Yang Xiaowei Chen Ming Zhou Wenjian Mo Caixia Wang Qinghua Cai Yumiao Li Ruiqing Zhou Shilin Xu Wei Zhou tingfen deng Shiyi Pan Yanli Xu Shunqing Wang Yuping Zhang 《Genes & Diseases》 SCIE CSCD 2024年第1期95-98,共4页
Increasing evidence supports the hypothesis of autologous immune attack in severe aplastic anemia(SAA):the predominant role of activated cytotoxic T cells(CTL)expressing-interferon in inhibiting the growth of bone mar... Increasing evidence supports the hypothesis of autologous immune attack in severe aplastic anemia(SAA):the predominant role of activated cytotoxic T cells(CTL)expressing-interferon in inhibiting the growth of bone marrow(BM)cells,putative autoantigens,and oligoclonal expansion of CD8+T cells.1 For SAA patients,the definitive therapies are immunosuppressive therapy(IST)or hematopoietic stem transplantation(HSCT). 展开更多
关键词 ANEMIA APLASTIC INTERFERON
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