{"title":"Physiological Level of Eosinophils Is Essential for the Regeneration and Homeostasis of Murine Hematopoietic Stem Cells","authors":"Chao Zhang, Weiwei Yi, Zhehua Shao, Bingpeng Yao, Guoxiong Tian, Fei Li, Xufei Du, Yangmingzi Hu, Yanqi Guo, Tao Wu, Wen Li, Zhihua Chen, Zhenyu Ju, Songmin Ying","doi":"10.1111/all.70021","DOIUrl":null,"url":null,"abstract":"BackgroundEosinophils play a crucial role in host defense and immunity, yet their regulatory functions within the hematopoietic homeostasis remain poorly understood. Our prior investigations revealed that pathologically elevated eosinophil levels in asthma not only disrupt bone marrow hematopoietic stem cell (HSC) quiescence but also establish a self‐reinforcing cycle of eosinophil lineage commitment. Here, we further investigate the critical role of physiologically steady‐state levels of eosinophils in maintaining HSC functions.MethodsUsing eosinophil lineage‐specific null (Eos‐null) mice, we established models of chemotherapy‐induced HSC regeneration and competitive bone marrow transplantation (cBMT) assay to evaluate the impact of eosinophil depletion on HSC regeneration and function. In vitro colony forming assay assessed HSC reconstitute capability, while bone marrow chimeric mice were established with wild‐type (WT) and eosinophil‐related transgenic mice to further elucidate the role of physiological levels of eosinophils. RNA‐seq and cytokine array analyses were utilized to investigate the potential protective mechanisms of eosinophils.ResultsCompared to WT controls, Eos‐null mice exhibited significantly impaired HSC regeneration, characterized by a diminished response to 5‐fluorouracil (5‐FU) and carboplatin treatment. Both long‐term HSCs (LT‐HSCs) and lineage<jats:sup>−</jats:sup>Sca‐1<jats:sup>+</jats:sup>c‐Kit<jats:sup>+</jats:sup> (LSK) demonstrated compromised reconstitution capacity in vivo and in vitro. HSCs from Eos‐null mice demonstrated elevated apoptosis under 5‐FU treatment, potentially due to the absence of eosinophil‐derived protective factors. Conversely, both chimeric mice and eosinophil incorporation within bone marrow transplantation systems significantly disrupted HSC homeostasis and function.ConclusionPhysiological eosinophil level is essential for maintaining HSC regeneration, reconstitution capacity, and homeostasis.","PeriodicalId":122,"journal":{"name":"Allergy","volume":"12 1","pages":""},"PeriodicalIF":12.0000,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Allergy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/all.70021","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0
Abstract
BackgroundEosinophils play a crucial role in host defense and immunity, yet their regulatory functions within the hematopoietic homeostasis remain poorly understood. Our prior investigations revealed that pathologically elevated eosinophil levels in asthma not only disrupt bone marrow hematopoietic stem cell (HSC) quiescence but also establish a self‐reinforcing cycle of eosinophil lineage commitment. Here, we further investigate the critical role of physiologically steady‐state levels of eosinophils in maintaining HSC functions.MethodsUsing eosinophil lineage‐specific null (Eos‐null) mice, we established models of chemotherapy‐induced HSC regeneration and competitive bone marrow transplantation (cBMT) assay to evaluate the impact of eosinophil depletion on HSC regeneration and function. In vitro colony forming assay assessed HSC reconstitute capability, while bone marrow chimeric mice were established with wild‐type (WT) and eosinophil‐related transgenic mice to further elucidate the role of physiological levels of eosinophils. RNA‐seq and cytokine array analyses were utilized to investigate the potential protective mechanisms of eosinophils.ResultsCompared to WT controls, Eos‐null mice exhibited significantly impaired HSC regeneration, characterized by a diminished response to 5‐fluorouracil (5‐FU) and carboplatin treatment. Both long‐term HSCs (LT‐HSCs) and lineage−Sca‐1+c‐Kit+ (LSK) demonstrated compromised reconstitution capacity in vivo and in vitro. HSCs from Eos‐null mice demonstrated elevated apoptosis under 5‐FU treatment, potentially due to the absence of eosinophil‐derived protective factors. Conversely, both chimeric mice and eosinophil incorporation within bone marrow transplantation systems significantly disrupted HSC homeostasis and function.ConclusionPhysiological eosinophil level is essential for maintaining HSC regeneration, reconstitution capacity, and homeostasis.
期刊介绍:
Allergy is an international and multidisciplinary journal that aims to advance, impact, and communicate all aspects of the discipline of Allergy/Immunology. It publishes original articles, reviews, position papers, guidelines, editorials, news and commentaries, letters to the editors, and correspondences. The journal accepts articles based on their scientific merit and quality.
Allergy seeks to maintain contact between basic and clinical Allergy/Immunology and encourages contributions from contributors and readers from all countries. In addition to its publication, Allergy also provides abstracting and indexing information. Some of the databases that include Allergy abstracts are Abstracts on Hygiene & Communicable Disease, Academic Search Alumni Edition, AgBiotech News & Information, AGRICOLA Database, Biological Abstracts, PubMed Dietary Supplement Subset, and Global Health, among others.