Cell stem cell最新文献

筛选
英文 中文
From suppressor to enhancer: IL-10's alternative role in CAR-T cell therapies against solid tumors. 从抑制剂到增强剂:IL-10 在 CAR-T 细胞疗法中对实体瘤的替代作用。
Cell stem cell Pub Date : 2024-03-07 DOI: 10.1016/j.stem.2024.02.003
Yuwei Huang, Haopeng Wang
{"title":"From suppressor to enhancer: IL-10's alternative role in CAR-T cell therapies against solid tumors.","authors":"Yuwei Huang, Haopeng Wang","doi":"10.1016/j.stem.2024.02.003","DOIUrl":"10.1016/j.stem.2024.02.003","url":null,"abstract":"<p><p>Aiming to improve the effector function of CAR-T cells, Zhao et al.<sup>1</sup> report that IL-10 metabolically reprograms CAR-T cells, and this promotes their effectiveness against solid tumors and challenges IL-10's perceived role as merely immunosuppressive. This simple but promising strategy fosters durable immune memory and eagerly awaits validation in clinical trials.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":"31 3","pages":"285-287"},"PeriodicalIF":0.0,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140066372","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development has the answer: Unraveling psychiatric disorders via thalamocortical organoids. 发育有了答案:通过丘脑皮层有机体揭开精神疾病的神秘面纱
Cell stem cell Pub Date : 2024-03-07 DOI: 10.1016/j.stem.2024.02.008
Eduardo Leyva-Díaz, Emily S Wilson, Guillermina López-Bendito
{"title":"Development has the answer: Unraveling psychiatric disorders via thalamocortical organoids.","authors":"Eduardo Leyva-Díaz, Emily S Wilson, Guillermina López-Bendito","doi":"10.1016/j.stem.2024.02.008","DOIUrl":"10.1016/j.stem.2024.02.008","url":null,"abstract":"<p><p>Dissecting the role of the thalamus in neuropsychiatric disorders requires new models to analyze complex genetic interactions. In this issue of Cell Stem Cell, Shin et al. use patient-derived thalamocortical organoids to investigate 22q11.2 microdeletion impact on thalamic development, revealing significant transcriptional dysregulation linked to psychiatric disorders.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":"31 3","pages":"283-284"},"PeriodicalIF":0.0,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140066371","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Promises and challenges of organoids: From humanized to human derived. 有机体的前景与挑战:从 "人源化 "到 "人源化"。
Cell stem cell Pub Date : 2024-03-07 DOI: 10.1016/j.stem.2024.02.002
Wenyan Wang, Yang-Xin Fu
{"title":"Promises and challenges of organoids: From humanized to human derived.","authors":"Wenyan Wang, Yang-Xin Fu","doi":"10.1016/j.stem.2024.02.002","DOIUrl":"10.1016/j.stem.2024.02.002","url":null,"abstract":"<p><p>Kastenschmidt et al.<sup>1</sup> present a groundbreaking organoid culture model for follicular lymphoma, which is capable of maintaining stable compositions of B and T cells. This model is utilized in testing bispecific antibodies in effective killing of tumor B cells with the activation of T cells.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":"31 3","pages":"281-282"},"PeriodicalIF":0.0,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140066375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Canonical Wnt signaling directs the generation of functional human PSC-derived atrioventricular canal cardiomyocytes in bioprinted cardiac tissues. 典型 Wnt 信号指导在生物打印心脏组织中生成功能性人类 PSC 衍生房室管心肌细胞。
Cell stem cell Pub Date : 2024-03-07 Epub Date: 2024-02-15 DOI: 10.1016/j.stem.2024.01.008
Chenxi Ye, Chuanlai Yang, Heqiang Zhang, Rui Gao, Yingnan Liao, Yali Zhang, Lingjun Jie, Yanhui Zhang, Tong Cheng, Yan Wang, Jie Ren
{"title":"Canonical Wnt signaling directs the generation of functional human PSC-derived atrioventricular canal cardiomyocytes in bioprinted cardiac tissues.","authors":"Chenxi Ye, Chuanlai Yang, Heqiang Zhang, Rui Gao, Yingnan Liao, Yali Zhang, Lingjun Jie, Yanhui Zhang, Tong Cheng, Yan Wang, Jie Ren","doi":"10.1016/j.stem.2024.01.008","DOIUrl":"10.1016/j.stem.2024.01.008","url":null,"abstract":"<p><p>The creation of a functional 3D bioprinted human heart remains challenging, largely due to the lack of some crucial cardiac cell types, including the atrioventricular canal (AVC) cardiomyocytes, which are essential to slow down the electrical impulse between the atrium and ventricle. By utilizing single-cell RNA sequencing analysis and a 3D bioprinting technology, we discover that stage-specific activation of canonical Wnt signaling creates functional AVC cardiomyocytes derived from human pluripotent stem cells. These cardiomyocytes display morphological characteristics and express molecular markers of AVC cardiomyocytes, including transcription factors TBX2 and MSX2. When bioprinted in prefabricated cardiac tissues, these cardiomyocytes successfully delay the electrical impulse, demonstrating their capability of functioning as the AVC cardiomyocytes in vitro. Thus, these findings not only identify canonical Wnt signaling as a key regulator of the AVC cardiomyocyte differentiation in vitro, but, more importantly, provide a critical cellular source for the biofabrication of a functional human heart.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":" ","pages":"398-409.e5"},"PeriodicalIF":0.0,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139747960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
KOLF2.1J iPSCs carry CNVs associated with neurodevelopmental disorders. KOLF2.1J iPSCs携带与神经发育障碍有关的CNV。
Cell stem cell Pub Date : 2024-03-07 DOI: 10.1016/j.stem.2024.02.007
Carolina Gracia-Diaz, Jonathan E Perdomo, Munir E Khan, Thomas Roule, Brianna L Disanza, Gregory G Cajka, Sunyimeng Lei, Alyssa L Gagne, Jean Ann Maguire, Ophir Shalem, Elizabeth J Bhoj, Rebecca C Ahrens-Nicklas, Deborah L French, Ethan M Goldberg, Kai Wang, Joseph T Glessner, Naiara Akizu
{"title":"KOLF2.1J iPSCs carry CNVs associated with neurodevelopmental disorders.","authors":"Carolina Gracia-Diaz, Jonathan E Perdomo, Munir E Khan, Thomas Roule, Brianna L Disanza, Gregory G Cajka, Sunyimeng Lei, Alyssa L Gagne, Jean Ann Maguire, Ophir Shalem, Elizabeth J Bhoj, Rebecca C Ahrens-Nicklas, Deborah L French, Ethan M Goldberg, Kai Wang, Joseph T Glessner, Naiara Akizu","doi":"10.1016/j.stem.2024.02.007","DOIUrl":"10.1016/j.stem.2024.02.007","url":null,"abstract":"","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":"31 3","pages":"288-289"},"PeriodicalIF":0.0,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11857058/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140066373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A time- and single-cell-resolved model of murine bone marrow hematopoiesis. 小鼠骨髓造血的时间和单细胞分辨模型
Cell stem cell Pub Date : 2024-02-01 Epub Date: 2024-01-05 DOI: 10.1016/j.stem.2023.12.001
Iwo Kucinski, Joana Campos, Melania Barile, Francesco Severi, Natacha Bohin, Pedro N Moreira, Lewis Allen, Hannah Lawson, Myriam L R Haltalli, Sarah J Kinston, Dónal O'Carroll, Kamil R Kranc, Berthold Göttgens
{"title":"A time- and single-cell-resolved model of murine bone marrow hematopoiesis.","authors":"Iwo Kucinski, Joana Campos, Melania Barile, Francesco Severi, Natacha Bohin, Pedro N Moreira, Lewis Allen, Hannah Lawson, Myriam L R Haltalli, Sarah J Kinston, Dónal O'Carroll, Kamil R Kranc, Berthold Göttgens","doi":"10.1016/j.stem.2023.12.001","DOIUrl":"10.1016/j.stem.2023.12.001","url":null,"abstract":"<p><p>The paradigmatic hematopoietic tree model is increasingly recognized to be limited, as it is based on heterogeneous populations largely defined by non-homeostatic assays testing cell fate potentials. Here, we combine persistent labeling with time-series single-cell RNA sequencing to build a real-time, quantitative model of in vivo tissue dynamics for murine bone marrow hematopoiesis. We couple cascading single-cell expression patterns with dynamic changes in differentiation and growth speeds. The resulting explicit linkage between molecular states and cellular behavior reveals widely varying self-renewal and differentiation properties across distinct lineages. Transplanted stem cells show strong acceleration of differentiation at specific stages of erythroid and neutrophil production, illustrating how the model can quantify the impact of perturbations. Our reconstruction of dynamic behavior from snapshot measurements is akin to how a kinetoscope allows sequential images to merge into a movie. We posit that this approach is generally applicable to understanding tissue-scale dynamics at high resolution.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":" ","pages":"244-259.e10"},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7615671/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139111392","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hallmarks of stemness in mammalian tissues. 哺乳动物组织干性的特征
IF 20.4
Cell stem cell Pub Date : 2024-01-04 DOI: 10.1016/j.stem.2023.12.006
Joep Beumer, Hans Clevers
{"title":"Hallmarks of stemness in mammalian tissues.","authors":"Joep Beumer, Hans Clevers","doi":"10.1016/j.stem.2023.12.006","DOIUrl":"10.1016/j.stem.2023.12.006","url":null,"abstract":"<p><p>All adult tissues experience wear and tear. Most tissues can compensate for cell loss through the activity of resident stem cells. Although the cellular maintenance strategies vary greatly between different adult (read: postnatal) tissues, the function of stem cells is best defined by their capacity to replace lost tissue through division. We discuss a set of six complementary hallmarks that are key enabling features of this basic function. These include longevity and self-renewal, multipotency, transplantability, plasticity, dependence on niche signals, and maintenance of genome integrity. We discuss these hallmarks in the context of some of the best-understood adult stem cell niches.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":"31 1","pages":"7-24"},"PeriodicalIF":20.4,"publicationDate":"2024-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10769195/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139107008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The KRAS tour: Studying metabolic reprogramming in isogenic pancreatic cancer organoids. KRAS 之旅:研究异源胰腺癌器官组织中的代谢重编程。
IF 20.4
Cell stem cell Pub Date : 2024-01-04 DOI: 10.1016/j.stem.2023.12.010
Shree Bose, Xiling Shen
{"title":"The KRAS tour: Studying metabolic reprogramming in isogenic pancreatic cancer organoids.","authors":"Shree Bose, Xiling Shen","doi":"10.1016/j.stem.2023.12.010","DOIUrl":"10.1016/j.stem.2023.12.010","url":null,"abstract":"<p><p>Using an isogenic organoid platform to model pancreatic cancer, Duan et al. establish an important link between mutant KRAS and cholesterol metabolism and identify perhexiline maleate as a possible therapeutic to target this relationship.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":"31 1","pages":"1-2"},"PeriodicalIF":20.4,"publicationDate":"2024-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139107009","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Decoding aging-dependent regenerative decline across tissues at single-cell resolution. 以单细胞分辨率解码跨组织的衰老依赖性再生衰退。
Cell stem cell Pub Date : 2023-12-07 Epub Date: 2023-10-27 DOI: 10.1016/j.stem.2023.09.014
Yusheng Cai, Muzhao Xiong, Zijuan Xin, Chengyu Liu, Jie Ren, Xiying Yang, Jinghui Lei, Wei Li, Feifei Liu, Qun Chu, Yiyuan Zhang, Jian Yin, Yanxia Ye, Dingyi Liu, Yanling Fan, Shuhui Sun, Yaobin Jing, Qian Zhao, Liyun Zhao, Shanshan Che, Yandong Zheng, Haoteng Yan, Shuai Ma, Si Wang, Juan Carlos Izpisua Belmonte, Jing Qu, Weiqi Zhang, Guang-Hui Liu
{"title":"Decoding aging-dependent regenerative decline across tissues at single-cell resolution.","authors":"Yusheng Cai, Muzhao Xiong, Zijuan Xin, Chengyu Liu, Jie Ren, Xiying Yang, Jinghui Lei, Wei Li, Feifei Liu, Qun Chu, Yiyuan Zhang, Jian Yin, Yanxia Ye, Dingyi Liu, Yanling Fan, Shuhui Sun, Yaobin Jing, Qian Zhao, Liyun Zhao, Shanshan Che, Yandong Zheng, Haoteng Yan, Shuai Ma, Si Wang, Juan Carlos Izpisua Belmonte, Jing Qu, Weiqi Zhang, Guang-Hui Liu","doi":"10.1016/j.stem.2023.09.014","DOIUrl":"10.1016/j.stem.2023.09.014","url":null,"abstract":"<p><p>Regeneration across tissues and organs exhibits significant variation throughout the body and undergoes a progressive decline with age. To decode the relationships between aging and regenerative capacity, we conducted a comprehensive single-cell transcriptome analysis of regeneration in eight tissues from young and aged mice. We employed diverse analytical models to study tissue regeneration and unveiled the intricate cellular and molecular mechanisms underlying the attenuated regenerative processes observed in aged tissues. Specifically, we identified compromised stem cell mobility and inadequate angiogenesis as prominent contributors to this age-associated decline in regenerative capacity. Moreover, we discovered a unique subset of Arg1<sup>+</sup> macrophages that were activated in young tissues but suppressed in aged regenerating tissues, suggesting their important role in age-related immune response disparities during regeneration. This study provides a comprehensive single-cell resource for identifying potential targets for interventions aimed at enhancing regenerative outcomes in the aging population.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":" ","pages":"1674-1691.e8"},"PeriodicalIF":0.0,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"66784770","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
VEGFA mRNA-LNP promotes biliary epithelial cell-to-hepatocyte conversion in acute and chronic liver diseases and reverses steatosis and fibrosis. VEGFA mRNA-LNP在急性和慢性肝病中促进胆道上皮细胞向肝细胞的转化,并逆转脂肪变性和纤维化。
Cell stem cell Pub Date : 2023-12-07 Epub Date: 2023-11-28 DOI: 10.1016/j.stem.2023.10.008
Fatima Rizvi, Yu-Ri Lee, Ricardo Diaz-Aragon, Pushpinder S Bawa, Juhoon So, Rodrigo M Florentino, Susan Wu, Arianna Sarjoo, Emily Truong, Anna R Smith, Feiya Wang, Elissa Everton, Alina Ostrowska, Kyounghwa Jung, Ying Tam, Hiromi Muramatsu, Norbert Pardi, Drew Weissman, Alejandro Soto-Gutierrez, Donghun Shin, Valerie Gouon-Evans
{"title":"VEGFA mRNA-LNP promotes biliary epithelial cell-to-hepatocyte conversion in acute and chronic liver diseases and reverses steatosis and fibrosis.","authors":"Fatima Rizvi, Yu-Ri Lee, Ricardo Diaz-Aragon, Pushpinder S Bawa, Juhoon So, Rodrigo M Florentino, Susan Wu, Arianna Sarjoo, Emily Truong, Anna R Smith, Feiya Wang, Elissa Everton, Alina Ostrowska, Kyounghwa Jung, Ying Tam, Hiromi Muramatsu, Norbert Pardi, Drew Weissman, Alejandro Soto-Gutierrez, Donghun Shin, Valerie Gouon-Evans","doi":"10.1016/j.stem.2023.10.008","DOIUrl":"10.1016/j.stem.2023.10.008","url":null,"abstract":"<p><p>The liver is known for its remarkable regenerative ability through proliferation of hepatocytes. Yet, during chronic injury or severe hepatocyte death, proliferation of hepatocytes is exhausted. To overcome this hurdle, we propose vascular-endothelial-growth-factor A (VEGFA) as a therapeutic means to accelerate biliary epithelial-cell (BEC)-to-hepatocyte conversion. Investigation in zebrafish establishes that blocking VEGF receptors abrogates BEC-driven liver repair, while VEGFA overexpression promotes it. Delivery of VEGFA via nonintegrative and safe nucleoside-modified mRNA encapsulated into lipid nanoparticles (mRNA-LNPs) in acutely or chronically injured mouse livers induces robust BEC-to-hepatocyte conversion and elimination of steatosis and fibrosis. In human and murine diseased livers, we further identified VEGFA-receptor KDR-expressing BECs associated with KDR-expressing cell-derived hepatocytes. This work defines KDR-expressing cells, most likely being BECs, as facultative progenitors. This study reveals unexpected therapeutic benefits of VEGFA delivered via nucleoside-modified mRNA-LNP, whose safety is widely validated with COVID-19 vaccines, for harnessing BEC-driven repair to potentially treat liver diseases.</p>","PeriodicalId":93928,"journal":{"name":"Cell stem cell","volume":" ","pages":"1640-1657.e8"},"PeriodicalIF":0.0,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10843608/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138465042","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书