Cargando…
Humanized CD36 (hCD36) mouse model supports the preclinical evaluation of therapeutic candidates targeting CD36
CD36 (also known as scavenger receptor B2) is a multifunctional receptor that mediates lipid uptake, advanced oxidation protein products, and immunological recognition, and has roles in lipid accumulation, apoptosis, as well as in metastatic colonization in cancer. CD36 is involved in tumor immunity...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Association for Laboratory Animal Science
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658083/ https://www.ncbi.nlm.nih.gov/pubmed/37407484 http://dx.doi.org/10.1538/expanim.23-0021 |
_version_ | 1785137353004679168 |
---|---|
author | Xie, Xiulong Niu, Zhenlan Wang, Linlin Zhou, Xiaofei Yu, Xingyan Jing, Hongyan Yang, Yi |
author_facet | Xie, Xiulong Niu, Zhenlan Wang, Linlin Zhou, Xiaofei Yu, Xingyan Jing, Hongyan Yang, Yi |
author_sort | Xie, Xiulong |
collection | PubMed |
description | CD36 (also known as scavenger receptor B2) is a multifunctional receptor that mediates lipid uptake, advanced oxidation protein products, and immunological recognition, and has roles in lipid accumulation, apoptosis, as well as in metastatic colonization in cancer. CD36 is involved in tumor immunity, metastatic invasion, and therapy resistance through various molecular mechanisms. Targeting CD36 has emerged as an effective strategy for tumor immunotherapy. In this study, we have successfully generated a novel hCD36 mouse (Unless otherwise stated, hCD36 mouse below refer to homozygous hCD36 mouse) strain where the sequences encoding the extracellular domains of the mouse Cd36 gene were replaced with the corresponding human sequences. The results showed that the hCD36 mice only expressed human CD36, and the proportion of each lymphocyte was not significantly changed compared with wild-type mice. Furthermore, CD36 monoclonal antibody could significantly inhibit tumor growth after treatment. Therefore, the hCD36 mouse represent a validated preclinical mouse model for the evaluation of tumor immunotherapy targeting CD36. |
format | Online Article Text |
id | pubmed-10658083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Japanese Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106580832023-01-01 Humanized CD36 (hCD36) mouse model supports the preclinical evaluation of therapeutic candidates targeting CD36 Xie, Xiulong Niu, Zhenlan Wang, Linlin Zhou, Xiaofei Yu, Xingyan Jing, Hongyan Yang, Yi Exp Anim Original CD36 (also known as scavenger receptor B2) is a multifunctional receptor that mediates lipid uptake, advanced oxidation protein products, and immunological recognition, and has roles in lipid accumulation, apoptosis, as well as in metastatic colonization in cancer. CD36 is involved in tumor immunity, metastatic invasion, and therapy resistance through various molecular mechanisms. Targeting CD36 has emerged as an effective strategy for tumor immunotherapy. In this study, we have successfully generated a novel hCD36 mouse (Unless otherwise stated, hCD36 mouse below refer to homozygous hCD36 mouse) strain where the sequences encoding the extracellular domains of the mouse Cd36 gene were replaced with the corresponding human sequences. The results showed that the hCD36 mice only expressed human CD36, and the proportion of each lymphocyte was not significantly changed compared with wild-type mice. Furthermore, CD36 monoclonal antibody could significantly inhibit tumor growth after treatment. Therefore, the hCD36 mouse represent a validated preclinical mouse model for the evaluation of tumor immunotherapy targeting CD36. Japanese Association for Laboratory Animal Science 2023-07-06 2023 /pmc/articles/PMC10658083/ /pubmed/37407484 http://dx.doi.org/10.1538/expanim.23-0021 Text en ©2023 Japanese Association for Laboratory Animal Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Xie, Xiulong Niu, Zhenlan Wang, Linlin Zhou, Xiaofei Yu, Xingyan Jing, Hongyan Yang, Yi Humanized CD36 (hCD36) mouse model supports the preclinical evaluation of therapeutic candidates targeting CD36 |
title | Humanized CD36 (hCD36) mouse model supports the preclinical evaluation of therapeutic candidates targeting CD36 |
title_full | Humanized CD36 (hCD36) mouse model supports the preclinical evaluation of therapeutic candidates targeting CD36 |
title_fullStr | Humanized CD36 (hCD36) mouse model supports the preclinical evaluation of therapeutic candidates targeting CD36 |
title_full_unstemmed | Humanized CD36 (hCD36) mouse model supports the preclinical evaluation of therapeutic candidates targeting CD36 |
title_short | Humanized CD36 (hCD36) mouse model supports the preclinical evaluation of therapeutic candidates targeting CD36 |
title_sort | humanized cd36 (hcd36) mouse model supports the preclinical evaluation of therapeutic candidates targeting cd36 |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658083/ https://www.ncbi.nlm.nih.gov/pubmed/37407484 http://dx.doi.org/10.1538/expanim.23-0021 |
work_keys_str_mv | AT xiexiulong humanizedcd36hcd36mousemodelsupportsthepreclinicalevaluationoftherapeuticcandidatestargetingcd36 AT niuzhenlan humanizedcd36hcd36mousemodelsupportsthepreclinicalevaluationoftherapeuticcandidatestargetingcd36 AT wanglinlin humanizedcd36hcd36mousemodelsupportsthepreclinicalevaluationoftherapeuticcandidatestargetingcd36 AT zhouxiaofei humanizedcd36hcd36mousemodelsupportsthepreclinicalevaluationoftherapeuticcandidatestargetingcd36 AT yuxingyan humanizedcd36hcd36mousemodelsupportsthepreclinicalevaluationoftherapeuticcandidatestargetingcd36 AT jinghongyan humanizedcd36hcd36mousemodelsupportsthepreclinicalevaluationoftherapeuticcandidatestargetingcd36 AT yangyi humanizedcd36hcd36mousemodelsupportsthepreclinicalevaluationoftherapeuticcandidatestargetingcd36 |