Cytokine & Growth Factor Reviews最新文献_第5页

Macrophage migration inhibitor factor (MIF): Potential role in cognitive impairment disorders 巨噬细胞迁移抑制因子 (MIF)：在认知障碍疾病中的潜在作用

IF 9.3 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-06-01 DOI: 10.1016/j.cytogfr.2024.03.003

Lian Zeng , Pengchao Hu , Yu Zhang , Mingyue Li , Yilin Zhao , Shiyong Li , Ailin Luo

{"title":"Macrophage migration inhibitor factor (MIF): Potential role in cognitive impairment disorders","authors":"Lian Zeng , Pengchao Hu , Yu Zhang , Mingyue Li , Yilin Zhao , Shiyong Li , Ailin Luo","doi":"10.1016/j.cytogfr.2024.03.003","DOIUrl":"10.1016/j.cytogfr.2024.03.003","url":null,"abstract":"<div><p>Macrophage migration inhibitory factor (MIF) is a cytokine in the immune system, participated in both innate and adaptive immune responses. Except from immune cells, MIF is also secreted by a variety of non-immune cells, including hematopoietic cells, endothelial cells (ECs), and neurons. MIF plays a crucial role in various diseases, such as sepsis, rheumatoid arthritis, acute kidney injury, and neurodegenerative diseases. The role of MIF in the neuropathogenesis of cognitive impairment disorders is emphasized, as it recruits multiple inflammatory mediators, leading to activating microglia or astrocyte-derived neuroinflammation. Furthermore, it contributes to the cell death of neurons and ECs with the binding of apoptosis-inducing factor (AIF) through parthanatos-associated apoptosis-inducing factor nuclease (PAAN) / MIF pathway. This review comprehensively delves into the relationship between MIF and the neuropathogenesis of cognitive impairment disorders, providing a series of emerging MIF-targeted pharmaceuticals as potential treatments for cognitive impairment disorders.</p></div>","PeriodicalId":11132,"journal":{"name":"Cytokine & Growth Factor Reviews","volume":"77 ","pages":"Pages 67-75"},"PeriodicalIF":9.3,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140271342","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Z-DNA binding protein 1 orchestrates innate immunity and inflammatory cell death Z-DNA 结合蛋白 1 协调先天免疫和炎症细胞死亡。

IF 9.3 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-06-01 DOI: 10.1016/j.cytogfr.2024.03.005

Qixiang Song , Yuhang Fan , Huali Zhang , Nian Wang

{"title":"Z-DNA binding protein 1 orchestrates innate immunity and inflammatory cell death","authors":"Qixiang Song , Yuhang Fan , Huali Zhang , Nian Wang","doi":"10.1016/j.cytogfr.2024.03.005","DOIUrl":"10.1016/j.cytogfr.2024.03.005","url":null,"abstract":"<div><p>Innate immunity is not only the first line of host defense against microbial infections but is also crucial for the host responses against a variety of noxious stimuli. Z-DNA binding protein 1 (ZBP1) is a cytosolic nucleic acid sensor that can induce inflammatory cell death in both immune and nonimmune cells upon sensing of incursive virus-derived Z-form nucleic acids and self-nucleic acids via its Zα domain. Mechanistically, aberrantly expressed or activated ZBP1 induced by pathogens or noxious stimuli enables recruitment of TANK binding kinase 1 (TBK1), interferon regulatory factor 3 (IRF3), receptor-interacting serine/threonine-protein kinase 1 (RIPK1) and RIPK3 to drive type I interferon (IFN-I) responses and activation of nuclear factor kappa B (NF-κB) signaling. Meanwhile, ZBP1 promotes the assembly of ZBP1- and absent in melanoma 2 (AIM2)-PANoptosome, which ultimately triggers PANoptosis through caspase 3-mediated apoptosis, mixed lineage kinase domain like pseudokinase (MLKL)-mediated necroptosis, and gasdermin D (GSDMD)-mediated pyroptosis. In response to damaged mitochondrial DNA, ZBP1 can interact with cyclic GMP-AMP synthase to augment IFN-I responses but inhibits toll like receptor 9-mediated inflammatory responses. This review summarizes the structure and expression pattern of ZBP1, discusses its roles in human diseases through immune-dependent (<em>e.g.</em>, the production of IFN-I and pro-inflammatory cytokines) and -independent (<em>e.g.</em>, the activation of cell death) functions, and highlights the attractive prospect of manipulating ZBP1 as a promising therapeutic target in diseases.</p></div>","PeriodicalId":11132,"journal":{"name":"Cytokine & Growth Factor Reviews","volume":"77 ","pages":"Pages 15-29"},"PeriodicalIF":9.3,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140317987","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Corrigendum to “Immune evasion of neutralizing antibodies by SARS-CoV-2 Omicron” [Cytokine Growth Factor Rev. 70 (2023) 13–25] 对 "SARS-CoV-2 Omicron 对中和抗体的免疫逃避 "的更正 [Cytokine Growth Factor Rev. 70 (2023) 13-25].

IF 9.3 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-06-01 DOI: 10.1016/j.cytogfr.2024.03.006

Lidong Wang , Michelle Møhlenberg , Pengfei Wang , Hao Zhou

引用次数: 0

Exogenous drug-induced mouse models of atopic dermatitis 外源性药物诱导的特应性皮炎小鼠模型

IF 9.3 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-06-01 DOI: 10.1016/j.cytogfr.2024.01.003

Rou Zheng , Yan Ren , Xinyue Liu , Canxia He , Hua Liu , Yixuan Wang , Jianing Li , Shuya Xia , Zhifang Liu , Yizhao Ma , Dianchen Wang , Suling Xu , Geng Wang , Na Li

{"title":"Exogenous drug-induced mouse models of atopic dermatitis","authors":"Rou Zheng , Yan Ren , Xinyue Liu , Canxia He , Hua Liu , Yixuan Wang , Jianing Li , Shuya Xia , Zhifang Liu , Yizhao Ma , Dianchen Wang , Suling Xu , Geng Wang , Na Li","doi":"10.1016/j.cytogfr.2024.01.003","DOIUrl":"10.1016/j.cytogfr.2024.01.003","url":null,"abstract":"<div><p>Atopic dermatitis (AD) is an inflammatory skin disease characterized by intense pruritus. AD is harmful to both children and adults, but its pathogenic mechanism has yet to be fully elucidated. The development of mouse models for AD has greatly contributed to its study and treatment. Among these models, the exogenous drug-induced mouse model has shown promising results and significant advantages. Until now, a large amount of AD-related research has utilized exogenous drug-induced mouse models, leading to notable advancements in research. This indicates the crucial significance of applying such models in AD research. These models exhibit diverse characteristics and are highly complex. They involve the use of various strains of mice, diverse types of inducers, and different modeling effects. However, there is currently a lack of comprehensive comparative studies on exogenous drug-induced AD mouse models, which hinders researchers' ability to choose among these models. This paper provides a comprehensive review of the features and mechanisms associated with various exogenous drug-induced mouse models, including the important role of each cytokine in AD development. It aims to assist researchers in quickly understanding models and selecting the most suitable one for further investigation.</p></div>","PeriodicalId":11132,"journal":{"name":"Cytokine & Growth Factor Reviews","volume":"77 ","pages":"Pages 104-116"},"PeriodicalIF":9.3,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139463027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

When pyro(ptosis) meets palm(itoylation) 当 "火烧"（ptosis）遇到 "棕榈"（itoylation）

IF 9.3 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-06-01 DOI: 10.1016/j.cytogfr.2024.03.001

Lu Jiang , Zirui Wang , Ting Xu , Leiliang Zhang

{"title":"When pyro(ptosis) meets palm(itoylation)","authors":"Lu Jiang , Zirui Wang , Ting Xu , Leiliang Zhang","doi":"10.1016/j.cytogfr.2024.03.001","DOIUrl":"10.1016/j.cytogfr.2024.03.001","url":null,"abstract":"<div><p>Pyroptosis, a programmed cell death process, is vital for the immune response against microbial infections and internal danger signals. Recent studies have highlighted the importance of protein palmitoylation, a modification that involves attaching palmitate to cysteine residues, in regulating key proteins involved in pyroptosis. Palmitoylation of cGAS at residue C474 by ZDHHC18 affects its enzymatic activity and DNA binding ability. Similarly, ZDHHC9 promotes cGAS activity through palmitoylation at residues C404/405. NLRP3 palmitoylation at residue C844, mediated by ZDHHC12, impacts its stability and interactions with other proteins, crucial for activating the NLRP3 inflammasome and triggering inflammation. However, the role of ZDHHC5 in NLRP3 palmitoylation remains uncertain due to conflicting findings. Palmitoylation at C88/91 is essential for STING activation and induction of type I interferons. It modulates the formation of multimeric complexes and downstream signaling pathways. GSDMD palmitoylation at C191 is necessary for pore formation and membrane translocation, while GSDME palmitoylation at C407/408 is associated with drug-induced pyroptosis. Moreover, palmitoylation of NOD1 and NOD2 influences their membrane recruitment and immune signaling pathways in response to bacterial peptidoglycans, acting as upstream regulators of pyroptosis. This review summarizes the important roles for palmitoylation in regulating the function of key pyroptosis-related proteins, shedding light on the intricate mechanisms governing immune responses and inflammation.</p></div>","PeriodicalId":11132,"journal":{"name":"Cytokine & Growth Factor Reviews","volume":"77 ","pages":"Pages 30-38"},"PeriodicalIF":9.3,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140054973","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Glycosylation of FGF/FGFR: An underrated sweet code regulating cellular signaling programs 成纤维细胞生长因子/成纤维细胞生长因子受体的糖基化：调节细胞信号程序的甜蜜密码。

IF 9.3 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-06-01 DOI: 10.1016/j.cytogfr.2024.04.001

Aleksandra Gędaj, Paulina Gregorczyk, Dominika Żukowska, Aleksandra Chorążewska, Krzysztof Ciura, Marta Kalka, Natalia Porębska, Łukasz Opaliński

{"title":"Glycosylation of FGF/FGFR: An underrated sweet code regulating cellular signaling programs","authors":"Aleksandra Gędaj, Paulina Gregorczyk, Dominika Żukowska, Aleksandra Chorążewska, Krzysztof Ciura, Marta Kalka, Natalia Porębska, Łukasz Opaliński","doi":"10.1016/j.cytogfr.2024.04.001","DOIUrl":"10.1016/j.cytogfr.2024.04.001","url":null,"abstract":"<div><p>Fibroblast growth factors (FGFs) and their receptors (FGFRs) constitute plasma-membrane localized signaling hubs that transmit signals from the extracellular environment to the cell interior, governing pivotal cellular processes like motility, metabolism, differentiation, division and death. FGF/FGFR signaling is critical for human body development and homeostasis; dysregulation of FGF/FGFR units is observed in numerous developmental diseases and in about 10% of human cancers. Glycosylation is a highly abundant posttranslational modification that is critical for physiological and pathological functions of the cell. Glycosylation is also very common within FGF/FGFR signaling hubs. Vast majority of FGFs (15 out of 22 members) are N-glycosylated and few FGFs are O-glycosylated. Glycosylation is even more abundant within FGFRs; all FGFRs are heavily N-glycosylated in numerous positions within their extracellular domains. A growing number of studies points on the multiple roles of glycosylation in fine-tuning FGF/FGFR signaling. Glycosylation modifies secretion of FGFs, determines their stability and affects interaction with FGFRs and co-receptors. Glycosylation of FGFRs determines their intracellular sorting, constitutes autoinhibitory mechanism within FGFRs and adjusts FGF and co-receptor recognition. Sugar chains attached to FGFs and FGFRs constitute also a form of code that is differentially decrypted by extracellular lectins, galectins, which transform FGF/FGFR signaling at multiple levels. This review focuses on the identified functions of glycosylation within FGFs and FGFRs and discusses their relevance for the cell physiology in health and disease.</p></div>","PeriodicalId":11132,"journal":{"name":"Cytokine & Growth Factor Reviews","volume":"77 ","pages":"Pages 39-55"},"PeriodicalIF":9.3,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1359610124000340/pdfft?md5=e4b6fce3e729f559c586c05301ce1a09&pid=1-s2.0-S1359610124000340-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140891806","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Unveiling the role of IL-17: Therapeutic insights and cardiovascular implications 揭示 IL-17 的作用：治疗见解和对心血管的影响。

IF 9.3 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-06-01 DOI: 10.1016/j.cytogfr.2024.05.001

Kexin Jiang , Yanjiani Xu , Yan Wang , Nanhao Yin , Fangyang Huang , Mao Chen

引用次数: 0

Interleukins and interferons in mesenchymal stromal stem cell-based gene therapy of cancer 白细胞介素和干扰素在基于间充质基质干细胞的癌症基因疗法中的应用。

IF 9.3 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-06-01 DOI: 10.1016/j.cytogfr.2024.03.002

Urban Švajger , Urška Kamenšek

{"title":"Interleukins and interferons in mesenchymal stromal stem cell-based gene therapy of cancer","authors":"Urban Švajger , Urška Kamenšek","doi":"10.1016/j.cytogfr.2024.03.002","DOIUrl":"10.1016/j.cytogfr.2024.03.002","url":null,"abstract":"<div><p>The tumor microenvironment is importantly shaped by various cytokines, where interleukins (ILs) and interferons (IFNs) shape the balance of immune activity within tumor niche and associated lymphoid organs. Their importance in activation and tuning of both innate and adaptive immune responses prompted their use in several clinical trials, albeit with limited therapeutic efficacy and risk of toxicity due to systemic administration. Increasing preclinical evidence suggests that local delivery of ILs and IFNs could significantly increase their effectiveness, while simultaneously attenuate the known side effects and issues related to their biological activity. A prominent way to achieve this is to use cell-based delivery vehicles. For this purpose, mesenchymal stromal stem cells (MSCs) are considered an almost ideal candidate. Namely, MSCs can be obtained in large quantities and from obtainable sources (e.g. umbilical cord or adipose tissue), their <em>ex vivo</em> expansion is relatively straightforward compared to other cell types and they possess very low immunogenicity making them suitable for allogeneic use. Importantly, MSCs have shown an intrinsic capacity to respond to tumor-directed chemotaxis. This review provides a focused and detailed discussion on MSC-based gene therapy using ILs and IFNs, engineering techniques and insights on potential future advancements.</p></div>","PeriodicalId":11132,"journal":{"name":"Cytokine & Growth Factor Reviews","volume":"77 ","pages":"Pages 76-90"},"PeriodicalIF":9.3,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140174106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Cytokines and soluble mediators as architects of tumor microenvironment reprogramming in cancer therapy 细胞因子和可溶性介质是癌症治疗中肿瘤微环境重编程的设计师

IF 13 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-02-28 DOI: 10.1016/j.cytogfr.2024.02.003

Suling Xu , Qingqing Wang , Wenxue Ma

{"title":"Cytokines and soluble mediators as architects of tumor microenvironment reprogramming in cancer therapy","authors":"Suling Xu , Qingqing Wang , Wenxue Ma","doi":"10.1016/j.cytogfr.2024.02.003","DOIUrl":"10.1016/j.cytogfr.2024.02.003","url":null,"abstract":"<div><p>Navigating the intricate landscape of the tumor microenvironment (TME) unveils a pivotal arena for cancer therapeutics, where cytokines and soluble mediators emerge as double-edged swords in the fight against cancer. This review ventures beyond traditional perspectives, illuminating the nuanced interplay of these elements as both allies and adversaries in cancer dynamics. It critically evaluates the evolving paradigms of TME reprogramming, spotlighting innovative strategies that target the sophisticated network of cytokines and mediators. Special focus is placed on unveiling the therapeutic potential of novel cytokines and mediators, particularly their synergistic interactions with extracellular vesicles, which represent underexplored conduits for therapeutic targeting. Addressing a significant gap in current research, we explore the untapped potential of these biochemical players in orchestrating immune responses, tumor proliferation, and metastasis. The review advocates for a paradigm shift towards exploiting these dynamic interactions within the TME, aiming to transcend conventional treatments and pave the way for a new era of precision oncology. Through a critical synthesis of recent advancements, we highlight the imperative for innovative approaches that harness the full spectrum of cytokine and mediator activities, setting the stage for breakthrough therapies that offer heightened specificity, reduced toxicity, and improved patient outcomes.</p></div>","PeriodicalId":11132,"journal":{"name":"Cytokine & Growth Factor Reviews","volume":"76 ","pages":"Pages 12-21"},"PeriodicalIF":13.0,"publicationDate":"2024-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140016975","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Semaphorins and the bone marrow microenvironment: New candidates that influence the hematopoietic system 半合成蛋白与骨髓微环境：影响造血系统的新候选者

IF 13 2区医学

Cytokine & Growth Factor Reviews Pub Date : 2024-02-27 DOI: 10.1016/j.cytogfr.2024.02.002

Carlos E. da Silva Gonçalves, Ricardo A. Fock

引用次数: 0