Innate immune control of liver regeneration

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Abstract/Contents

Abstract
Eosinophil-derived IL-4 stimulates hepatocyte proliferation to promote liver regeneration Abstract It has been proposed that allergic immune responses, like those mediated by type 2 immunity, evolved to protect the host from damage caused by environmental challenges, including toxins, xenobiotics, and helminth infections (1, 2). Despite some support for this hypothesis (3, 4), the underlying mechanisms by which type 2 innate responses orchestrate the regeneration of injured tissues remain largely unknown. Here, we demonstrate a requirement for type 2 innate immunity in regeneration of liver after partial hepatectomy and toxin-mediated injury. Injury to liver results in rapid recruitment of eosinophils, which secrete IL-4 to promote the proliferation of quiescent hepatocytes. Surprisingly, signaling via the IL-4R[alpha] in macrophages, which have been implicated in tissue repair (3-5), is dispensable for hepatocyte proliferation and liver regrowth after injury. Instead, IL-4 exerts its mitogenic actions by directly activating IL-4R[alpha] in hepatocytes. Our findings have thus uncovered an unexpected mechanism by which allergic type 2 innate immunity stimulates hepatocyte proliferation to promote liver regeneration.

Description

Type of resource text
Form electronic; electronic resource; remote
Extent 1 online resource.
Publication date 2013
Issuance monographic
Language English

Creators/Contributors

Associated with Goh, Yun Pei Sharon
Associated with Stanford University, Program in Immunology.
Primary advisor Steinman, Lawrence
Thesis advisor Steinman, Lawrence
Thesis advisor Chawla, Ajay
Thesis advisor Galli, Stephen J
Thesis advisor Martinez, Olivia
Advisor Chawla, Ajay
Advisor Galli, Stephen J
Advisor Martinez, Olivia

Subjects

Genre Theses

Bibliographic information

Statement of responsibility Yun Pei Sharon Goh.
Note Submitted to the Program in Immunology.
Thesis Thesis (Ph.D.)--Stanford University, 2013.
Location electronic resource

Access conditions

Copyright
© 2013 by Yun Pei Sharon Goh
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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