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Transcriptional and Translational Re...

Frias, Adolfo B.

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Transcriptional and Translational Regulators: Roles in Development and Function of Innate-Like and Adaptive Regulatory T Cells.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Transcriptional and Translational Regulators: Roles in Development and Function of Innate-Like and Adaptive Regulatory T Cells./
作者:	Frias, Adolfo B.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2020,
面頁冊數:	116 p.
附註:	Source: Dissertations Abstracts International, Volume: 82-06, Section: B.
Contained By:	Dissertations Abstracts International82-06B.
標題:	Immunology. -
電子資源:	https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=27828947
ISBN:	9798672196077

Transcriptional and Translational Regulators: Roles in Development and Function of Innate-Like and Adaptive Regulatory T Cells.
Frias, Adolfo B.

Transcriptional and Translational Regulators: Roles in Development and Function of Innate-Like and Adaptive Regulatory T Cells. - Ann Arbor : ProQuest Dissertations & Theses, 2020 - 116 p.

Source: Dissertations Abstracts International, Volume: 82-06, Section: B.

Thesis (Ph.D.)--University of Pittsburgh, 2020.

This item must not be sold to any third party vendors.

Invariant natural killer T (iNKT) cells and regulatory T cells (Tregs) both have roles in maintaining immune homeostasis. However, following disease, these cells often undergo loss of function and reduction in cell frequency. Invariant natural killer T (iNKT) cells are innate-like T lymphocytes capable of rapidly producing cytokines post-stimulation with the potent iNKT cell activator α-Galactosylceramide (α-GalCer). Due to iNKT cell's rapid effector cytokine production, we investigated the function of microRNAs (miRNAs) in iNKT cells, which are translational regulators that can quickly modulate regulation of protein synthesis. While miRNAs have been described in the development of iNKT cell development, no miRNAs had been ascribed to their effector function. We investigated whether microRNA-155 (miR-155) played a role in regulating the effector function of iNKT cells, as it was already shown to do so in CD8+ T cells and NK cells. Although we verified that miR-155 was upregulated in iNKT cells post α-GalCer stimulation, we found that miR-155 deficiency did not have an impact on iNKT cell cytokine production. Considering iNKT cells regulatory functions in maintaining immune homeostasis, miR-155 could be a potential therapeutic target to disrupt effector function in other immune cells while maintaining the effector function in iNKT cells. We also investigated the role of the transcriptional regulator Id2 in adipose-resident Tregs (aTregs). Inhibitor of DNA binding (Id) proteins are transcriptional regulators that dimerize with E protein transcription factors to inhibit their binding to E box sites and thus, prevent their activity. We verified that Id2 was upregulated in aTregs compared to higher Id3 expression in splenic Tregs. Under standard diet, loss of Id2 in aTregs led to a phenotype seen in high-fat-diet fed mice including a decrease in frequency and canonical aTreg markers including ST2, CCR2, KLRG1, and GATA3. Additionally, Id2 deficiency in Tregs led to increased systemic inflammation and impaired glucose tolerance. In essence Id2 expression was necessary for the aTreg transcriptional program including regulation of aTreg function to mediate tissue homeostasis. In summary, this thesis helps illuminate the unique influence of transcriptional and translational regulation on aTreg and iNKT cells which is critical for immune homeostasis.

ISBN: 9798672196077Subjects--Topical Terms:

611031
Immunology.
Subjects--Index Terms:

immune homeostasis

Transcriptional and Translational Regulators: Roles in Development and Function of Innate-Like and Adaptive Regulatory T Cells.
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520 $a Invariant natural killer T (iNKT) cells and regulatory T cells (Tregs) both have roles in maintaining immune homeostasis. However, following disease, these cells often undergo loss of function and reduction in cell frequency. Invariant natural killer T (iNKT) cells are innate-like T lymphocytes capable of rapidly producing cytokines post-stimulation with the potent iNKT cell activator α-Galactosylceramide (α-GalCer). Due to iNKT cell's rapid effector cytokine production, we investigated the function of microRNAs (miRNAs) in iNKT cells, which are translational regulators that can quickly modulate regulation of protein synthesis. While miRNAs have been described in the development of iNKT cell development, no miRNAs had been ascribed to their effector function. We investigated whether microRNA-155 (miR-155) played a role in regulating the effector function of iNKT cells, as it was already shown to do so in CD8+ T cells and NK cells. Although we verified that miR-155 was upregulated in iNKT cells post α-GalCer stimulation, we found that miR-155 deficiency did not have an impact on iNKT cell cytokine production. Considering iNKT cells regulatory functions in maintaining immune homeostasis, miR-155 could be a potential therapeutic target to disrupt effector function in other immune cells while maintaining the effector function in iNKT cells. We also investigated the role of the transcriptional regulator Id2 in adipose-resident Tregs (aTregs). Inhibitor of DNA binding (Id) proteins are transcriptional regulators that dimerize with E protein transcription factors to inhibit their binding to E box sites and thus, prevent their activity. We verified that Id2 was upregulated in aTregs compared to higher Id3 expression in splenic Tregs. Under standard diet, loss of Id2 in aTregs led to a phenotype seen in high-fat-diet fed mice including a decrease in frequency and canonical aTreg markers including ST2, CCR2, KLRG1, and GATA3. Additionally, Id2 deficiency in Tregs led to increased systemic inflammation and impaired glucose tolerance. In essence Id2 expression was necessary for the aTreg transcriptional program including regulation of aTreg function to mediate tissue homeostasis. In summary, this thesis helps illuminate the unique influence of transcriptional and translational regulation on aTreg and iNKT cells which is critical for immune homeostasis.
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