Immune regulation in the tissue barriers
Tissue barriers are physical interfaces that cover the organs and protect individuals from toxins and pathogens of the external environment. These protective layers consist of a variety of cells, where the stromal cells support tissue structures, provide environmental cues, and interact with the tissue-resident immune cells to sustain physiological function and immune homeostasis.
Our lab is interested in a fundamental biological question of how immune homeostasis is achieved in tissue barriers. We study how cells of the immune system adapt to environmental factors and acquire immune-modulatory functions to support tissue homeostasis. These studies will advance our understanding of mechanisms that render regulatory functions to tissue-resident immune cells and eventually prevent the undesirable immune responses which may lead to allergies, autoimmune disorders, recurrent infections, and increased risks of cancer.
Through analysis of immune cells in the tissue barriers, we identified novel niches at the CNS borders for B cell lymphopoiesis. We also found a novel eosinophil subset unique to the small intestine that modulates the type 2 immune responses. To acquire more insights into the immune regulations in the meninges and small intestine, we are focusing on the studies of 1. B cell tolerance in the meninges. 2) Meningeal B cells in neurodegeneration diseases. 3) Eosinophils in host defense and gut mucosal immunity.
- Postdoctoral Research Associate, 2019-2022, Washington University in St. Louis, USA
- Ph.D., 2019, Irell & Manella Graduate School of Biological Science at City of Hope, USA
- MS, 2009, Graduate Institute of Immunology, National Taiwan University, Taiwan
- BS, 2007, Dept. Chemistry, National Taiwan University, Taiwan
- Wei-Le Wang+, Jun Kasamatsu+, Satoru Joshita+, Susan Gilfillan, Blanda Di Luccia, Santosh K Panda, Do-Hyun Kim, Pritesh Desai, Jennifer K Bando, Stanley Ching-Cheng Huang, Kentaro Yomogida, Hitomi Hoshino, Mana Fukushima, Elizabeth A Jacobsen, Steven J Van Dyken, Christiane Ruedl, Marina Cella, Marco Colonna. +Equal contributions.(2022) The aryl hydrocarbon receptor instructs the immunomodulatory profile of a subset of Clec4a4+ eosinophils unique to the small intestine. PNAS, 2022 Jun 7;119(23): e2204557119.
- Wei-Le Wang, Ching Ouyang, Natalie M. Graham, Yaunkun Zhang, Kaniel Cassady, Estefany Y. Reyes, Min Xiong, Alicia M. Davis, Kathie Tang, Defu Zeng and Mark P. Boldin. (2022) microRNA-142 guards against autoimmunity by controlling Treg cell homeostasis and function. PLOS Biology, 2022 Feb 18;20(2): e3001552.
- Simone Brioschi+, Wei-Le Wang+, Vincent Peng+, Meng Wang Irina Shchukina, Zev J. Greenberg, Jennifer K. Bando, Natalia Jaeger, Rafael S. Czepielewski, Amanda Swain, Denis A. Mogilenko, Wandy Beatty, Peter Bayguinov, James A.J. Fitzpatrick6, Laura G. Schuettpelz, Catrina Fronick, Igor Smirnov, Jonathan Kipnis, Virginia S. Shapiro, Gregory F. Wu, Susan Gilfillan, Marina Cella, Maxim N. Artyomov, Steven H. Kleinstein, Marco Colonna. +Equal contributions.(2021) Heterogeneity of meningeal B cells reveals a lymphopoietic niche at the CNS borders. Science, 2021 Jul 23;373(6553): eabf9277.
- Nathaniel Magilnick, Estefany Reyes, Wei-Le Wang, Steven L. Vonderfecht, Jin Gohda, Jun-Ichiro Inoue, Mark P. Boldin.(2017) miR-146a–Traf6 regulatory axis controls autoimmunity and myelopoiesis, but is dispensable for hematopoietic stem cell homeostasis and tumor suppression. PNAS, 2017 Aug 22;114(34): E7140-E7149.
- Nicholas J. Kramer+, Wei-Le Wang+, Estefany Y. Reyes, Bijender Kumar, Ching-Cheng Chen, Ramakrishna Chandran, Edouard M. Cantin, Konstantin D. Taganov, Nelson Chau, and Mark P. Boldin. +Equal contributions.(2015) Altered lymphopoiesis and immunodeficiency in miR-142 null mice. Blood, 2015 Jun 11;125(24):3720-30.