News Release

How the regulator is regulated -- Insight into immune-related protein holds therapeutic value

Scientists unravel how the immune checkpoint protein PD-L2 is regulated, which has potential implications in immune therapy

Peer-Reviewed Publication

Tokyo University of Science

Immune Checkpoint Protein

image: Scientists find out how an immune checkpoint protein called PD-L2, which is expressed on the surface of a type of immune cells, is regulated at the molecular level. view more 

Credit: Tokyo University of Science

In immune-related disorders, therapy often involves identifying the molecules responsible for immune dysregulation and targeting them using drugs. This type of immune therapy is also used for cancer treatment, owing to the important role that immune cells play in cancer progression. One such type of a potential therapeutic target is an "immune checkpoint" protein called PD-L2, which is specifically expressed in immune cells called dendritic cells (DCs) and macrophages. PD-L2 plays various important functions in the regulation of different types of immune cells, including the suppression of T cells. Not surprisingly, this molecule has been extensively explored as a target protein in immunology and cancer immunology. But, despite years of research, exactly how this protein gets regulated has remained unclear until now.

Recently, a group of researchers at Tokyo University of Science, led by Professor Chiharu Nishiyama, made a significant leap towards this direction. In a new study published in the Journal of Immunology, the scientists dug deeper into the genetic and molecular basis of PD-L2 regulation. Prof Nishiyama says, "In our study, we investigated the gene expression mechanism of PD-L2, a cell-surface molecule that is specifically expressed in DCs and macrophages.''

The scientists began by focusing on DCs, which train other immune cells such as T cells to initiate a defense response against foreign molecules and cancer cells. In DCs, PD-L2 acts as a "checkpoint" that ensures that the immune cells do not incorrectly destroy healthy cells. Because the gene "Pdcd1lg2" is responsible for coding the PD-L2 protein, the scientists wanted to understand how this gene is regulated. A gene expresses its encoded protein through a series of coordinated cellular events that includes structural changes in the DNA caused by proteins known as "transcription factors," which bind to specific "regulatory" positions on the DNA. As the scientists wanted to know the exact events in PD-L2 regulation, they designed their experiments focusing on factors that regulate Pdcd1lg2. Previous studies had indicated that a transcription factor called PU.1 was involved in the development of other similar immune cells. The scientists wondered: was PU.1 involved in PD-L2 expression, too? Prof Nishiyama explains, "Previous studies had shown that the artificial expression of PU.1 on non-dendritic immune cells transformed these cells into DCs. This made us think if PU.1 had any role in the expression of PD-L2, one of the prominent surface proteins of DCs."

To begin with, the scientists studied the effect of "knocking down" PU.1 and a few other proteins in cell models. They found that in the absence of PU.1 and its associate molecule IRF4, the expression of PD-L2 was severely compromised. Once it was clear that PU.1 and IRF4 were involved in regulating the expression of PD-L2, the scientists carried out subsequent experiments using techniques such as "chromatin immunoprecipitation" to know exactly how this happens. They found out that PU.1 and IRF4 together bind to a region on the DNA called the "EICE sequence" and stimulate the expression of Pdcd1lg2 gene. It also became clear that PU.1 indirectly plays a role in altering the DNA molecule to a "relaxed" form by inducing chemical changes in the "histone" proteins, which are bound to the DNA in its "condensed" form. These chemical changes are also called "epigenetic modifications" and form an important regulatory mechanism for gene/protein expression in these cells.

In sum, this study sheds light on the molecular events that take place in the regulation of the PD-L2 protein. This paves the way for further development of drugs that can regulate this protein in immune disorders. Prof Nishiyama concludes, "We believe that our findings have remarkable potential to improve the therapeutic approach against immune system-mediated diseases."


About The Tokyo University of Science

Tokyo University of Science (TUS) is a well-known and respected university, and the largest science-specialized private research university in Japan, with four campuses in central Tokyo and its suburbs and in Hokkaido. Established in 1881, the university has continually contributed to Japan's development in science through inculcating the love for science in researchers, technicians, and educators.

With a mission of "Creating science and technology for the harmonious development of nature, human beings, and society", TUS has undertaken a wide range of research from basic to applied science. TUS has embraced a multidisciplinary approach to research and undertaken intensive study in some of today's most vital fields. TUS is a meritocracy where the best in science is recognized and nurtured. It is the only private university in Japan that has produced a Nobel Prize winner and the only private university in Asia to produce Nobel Prize winners within the natural sciences field.


About Professor Chiharu Nishiyama from Tokyo University of Science

Professor Chiharu Nishiyama is a Professor at Tokyo University of Science. She is affiliated with Faculty of Industrial Science and Technology, Department of Biological Science and Technology. She received her Bachelor's, Master's, and PhD degree from The University of Tokyo in 1988, 1990, and 1997, respectively. Her main areas of research include applied biochemistry, immunology, allergy, molecular biology, transcription factor, and cell development. Prof Nishiyama was awarded the JSBBA Award for Young Scientists in 2005. Till date, she has around 115 research papers to her credit.

Funding information

This work was supported by a Grant-in-Aid for Scientific Research (B) (CN), Grant-in-Aid for Scientific Research (C) (TY and KK), the MEXT-Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science), the Tokyo Biochemical Research Foundation (CN), the Tojuro Iijima Foundation for Food Science and Technology (CN and TY), and the Takeda Science Foundation (CN).

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