Protective effects of Ganoderma lucidum spores on estradiol benzoate-induced TEC apoptosis and compromised double-positive thymocyte development

<b>Backgroud:</b> Thymic atrophy marks the onset of immune aging, precipitating developmental anomalies in T cells. Numerous clinical and preclinical investigations have underscored the regulatory role of <i>Ganoderma lucidum</i> spores (GLS) in T cell development. However, the precise mechanisms underlying this regulation remain elusive. <b>Methods:</b> In this study, a mice model of estradiol benzoate (EB)-induced thymic atrophy was constructed, and the improvement effect of GLS on thymic atrophy was evaluated. Then, we employs multi-omics techniques to elucidate how GLS modulates T cell development amidst EB-induced thymic atrophy in mice. <b>Results:</b> GLS effectively mitigates EB-induced thymic damage by attenuating apoptotic thymic epithelial cells (TECs) and enhancing the output of CD4<sup>+</sup> T cells into peripheral blood. During thymic T cell development, sporoderm-removed GLS (RGLS) promotes T cell receptor (TCR) α rearrangement by augmenting V-J fragment rearrangement frequency and efficiency. Notably, biased Vα14-Jα18 rearrangement fosters double-positive (DP) to invariant natural killer T (iNKT) cell differentiation, partially contingent on RGLS-mediated restriction of peptide-major histocompatibility complex I (pMHCⅠ)-CD8 interaction and augmented CD1d expression in DP thymocytes, thereby promoting DP to CD4<sup>+</sup> iNKT cell development. Furthermore, RGLS amplifies interaction between a DP subpopulation, termed DPsel-7, and plasmacytoid dendritic cells (pDCs), likely facilitating the subsequent development of double-negative iNKT1 cells. Lastly, RGLS suppresses EB-induced upregulation of Abpob and Apoa4, curbing the clearance of CD4<sup>+</sup>Abpob<sup>+</sup> and CD4<sup>+</sup>Apoa4<sup>+</sup> T cells by mTECs, resulting in enhanced CD4<sup>+</sup> T cell output. <b>Discussion:</b> These findings indicate that the RGLS effectively mitigates EB-induced TEC apoptosis and compromised double-positive thymocyte development. These insights into RGLS's immunoregulatory role pave the way for its potential as a T-cell regeneration inducer.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2024-08-16
DOI
https://doi.org/10.3389/fphar.2024.1419881
Citations
6
Primary Topic
Fungal Biology and Applications
Type
article
Field-Weighted Citation Impact
2.69

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article

Protective effects of Ganoderma lucidum spores on estradiol benzoate-induced TEC apoptosis and compromised double-positive thymocyte development

Guoliang Zhang, Jihong Yang, Haitao Pan, Anyao Li et al.
6 citations
Frontiers in Pharmacology
Fungal Biology and Applications
2.69
article

Protective effects of Ganoderma lucidum spores on estradiol benzoate-induced TEC apoptosis and compromised double-positive thymocyte development

Guoliang Zhang, Jihong Yang, Haitao Pan, Anyao Li, Zhenhao Li, Mengyao Wang, Xiaohui Fan
article en
6 citations

Abstract

<b>Backgroud:</b> Thymic atrophy marks the onset of immune aging, precipitating developmental anomalies in T cells. Numerous clinical and preclinical investigations have underscored the regulatory role of <i>Ganoderma lucidum</i> spores (GLS) in T cell development. However, the precise mechanisms underlying this regulation remain elusive. <b>Methods:</b> In this study, a mice model of estradiol benzoate (EB)-induced thymic atrophy was constructed, and the improvement effect of GLS on thymic atrophy was evaluated. Then, we employs multi-omics techniques to elucidate how GLS modulates T cell development amidst EB-induced thymic atrophy in mice. <b>Results:</b> GLS effectively mitigates EB-induced thymic damage by attenuating apoptotic thymic epithelial cells (TECs) and enhancing the output of CD4<sup>+</sup> T cells into peripheral blood. During thymic T cell development, sporoderm-removed GLS (RGLS) promotes T cell receptor (TCR) α rearrangement by augmenting V-J fragment rearrangement frequency and efficiency. Notably, biased Vα14-Jα18 rearrangement fosters double-positive (DP) to invariant natural killer T (iNKT) cell differentiation, partially contingent on RGLS-mediated restriction of peptide-major histocompatibility complex I (pMHCⅠ)-CD8 interaction and augmented CD1d expression in DP thymocytes, thereby promoting DP to CD4<sup>+</sup> iNKT cell development. Furthermore, RGLS amplifies interaction between a DP subpopulation, termed DPsel-7, and plasmacytoid dendritic cells (pDCs), likely facilitating the subsequent development of double-negative iNKT1 cells. Lastly, RGLS suppresses EB-induced upregulation of Abpob and Apoa4, curbing the clearance of CD4<sup>+</sup>Abpob<sup>+</sup> and CD4<sup>+</sup>Apoa4<sup>+</sup> T cells by mTECs, resulting in enhanced CD4<sup>+</sup> T cell output. <b>Discussion:</b> These findings indicate that the RGLS effectively mitigates EB-induced TEC apoptosis and compromised double-positive thymocyte development. These insights into RGLS's immunoregulatory role pave the way for its potential as a T-cell regeneration inducer.

Frontiers in PharmacologyVol. 15
Zhejiang Lab (CN), Hangzhou Botanical Garden (CN), Zhejiang University (CN)
National Natural Science Foundation of China, Natural Science Foundation for Young Scientists of Shanxi Province, Young Scientists Fund
Openalex Percentile: Top 10%
Fungal Biology and Applications
2.69
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