Folr2-flox Mouse
Common Name
Folr2-flox
제품 ID
S-CKO-02474
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-14276-Folr2-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Folr2-flox Mouse (카탈로그 번호 S-CKO-02474)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
기본 정보
품종 계통
Folr2-flox
품종 계통계통 ID
CKOCMP-14276-Folr2-B6J-VA
유전자명
제품 ID
S-CKO-02474
유전자 별칭
FBP2, FR-P3, Folbp2, FR-beta, Folbp-2
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 7
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000210598
NCBI 전사체 ID
NM_001303239
타겟 영역
Exon 4~6
유효 영역 크기
~1.3 kb
유전자 연구 개요
Folr2, the folate receptor 2, is one of the folate transporters and is known to be involved in folate-related processes. Folates are B vitamins crucial for one-carbon metabolism, and Folr2's role in this context may have implications for various cellular functions [6].
Folr2-expressing macrophages have been identified in multiple disease-related contexts. In breast cancer, FOLR2+ tissue-resident macrophages localize in perivascular areas of the tumor stroma, interact with CD8+ T cells, and their density positively correlates with better patient survival, suggesting a role in antitumor immunity [1]. In hepatocellular carcinoma, there is a re-emergence of fetal-like (FOLR2) tumor-associated macrophages as part of an onco-fetal reprogramming of the tumor microenvironment [2]. In chronic kidney disease, CXCL-iFibro fibroblasts promote the switch of macrophages into FOLR2+ macrophages, and this interaction is involved in fibrosis progression [3]. In colon cancer, a subset of FOLR2+ macrophages is embedded in plasma cell niches [4]. In gastric cancer, FOLR2+ macrophages possess antitumor immune potential, but their proportion decreases during the progression from intestinal metaplasia to early gastric cancer [5]. In lung adenocarcinoma, FOLR2-expressing tumor-associated macrophages may be involved in the formation of an immunosuppressive microenvironment through a trajectory related to regulatory T cells [7]. Also, TIM4+FOLR2+ macrophages in tertiary lymphoid structures across several cancer types are associated with an active immune infiltrate, and the TIM4+FOLR2+ macrophage subsets have different prognostic implications [8].
In conclusion, Folr2, through its association with macrophages, plays diverse roles in cancer and chronic kidney disease. In cancers, it can either be associated with promoting antitumor immunity or contributing to immunosuppressive microenvironments. In chronic kidney disease, it is involved in the fibrotic process. The study of Folr2 in these disease conditions helps in understanding the underlying immune-related and disease-progression mechanisms, potentially providing new therapeutic targets.
References:
1. Nalio Ramos, Rodrigo, Missolo-Koussou, Yoann, Gerber-Ferder, Yohan, Piaggio, Eliane, Helft, Julie. 2022. Tissue-resident FOLR2+ macrophages associate with CD8+ T cell infiltration in human breast cancer. In Cell, 185, 1189-1207.e25. doi:10.1016/j.cell.2022.02.021. https://pubmed.ncbi.nlm.nih.gov/35325594/
2. Sharma, Ankur, Seow, Justine Jia Wen, Dutertre, Charles-Antoine, Ginhoux, Florent, DasGupta, Ramanuj. 2020. Onco-fetal Reprogramming of Endothelial Cells Drives Immunosuppressive Macrophages in Hepatocellular Carcinoma. In Cell, 183, 377-394.e21. doi:10.1016/j.cell.2020.08.040. https://pubmed.ncbi.nlm.nih.gov/32976798/
3. Cohen, Camille, Mhaidly, Rana, Croizer, Hugo, Ju, Wenjun, Mechta-Grigoriou, Fatima. 2024. WNT-dependent interaction between inflammatory fibroblasts and FOLR2+ macrophages promotes fibrosis in chronic kidney disease. In Nature communications, 15, 743. doi:10.1038/s41467-024-44886-z. https://pubmed.ncbi.nlm.nih.gov/38272907/
4. Matusiak, Magdalena, Hickey, John W, van IJzendoorn, David G P, West, Robert B, van de Rijn, Matt. . Spatially Segregated Macrophage Populations Predict Distinct Outcomes in Colon Cancer. In Cancer discovery, 14, 1418-1439. doi:10.1158/2159-8290.CD-23-1300. https://pubmed.ncbi.nlm.nih.gov/38552005/
5. He, Yuxin, Wang, Jiayu, Deng, Zilin, Shi, Tongguo, Chen, Weichang. 2024. FOLR2+ macrophage depletion from intestinal metaplasia to early gastric cancer: single-cell sequencing insight into gastric cancer progression. In Journal of experimental & clinical cancer research : CR, 43, 326. doi:10.1186/s13046-024-03245-y. https://pubmed.ncbi.nlm.nih.gov/39702278/
6. Nawaz, Fathima Zahra, Kipreos, Edward T. 2022. Emerging roles for folate receptor FOLR1 in signaling and cancer. In Trends in endocrinology and metabolism: TEM, 33, 159-174. doi:10.1016/j.tem.2021.12.003. https://pubmed.ncbi.nlm.nih.gov/35094917/
7. Xiang, Chan, Zhang, Min, Shang, Zhanxian, Yu, Yang, Han, Yuchen. 2023. Single-cell profiling reveals the trajectory of FOLR2-expressing tumor-associated macrophages to regulatory T cells in the progression of lung adenocarcinoma. In Cell death & disease, 14, 493. doi:10.1038/s41419-023-06021-6. https://pubmed.ncbi.nlm.nih.gov/37532692/
8. Bugatti, Mattia, Bergamini, Marco, Missale, Francesco, Benvenuti, Federica, Vermi, William. . A Population of TIM4+FOLR2+ Macrophages Localized in Tertiary Lymphoid Structures Correlates to an Active Immune Infiltrate Across Several Cancer Types. In Cancer immunology research, 10, 1340-1353. doi:10.1158/2326-6066.CIR-22-0271. https://pubmed.ncbi.nlm.nih.gov/36122412/
품질 관리 기준
정자 검사
동결 보존 전: 정자 농도 측정 및 정자 생존율 평가.
동결 보존 후: 각 배치에서 동결 보존된 정자 바이알 1개를 선택하여 체외수정(in vitro fertilization)에 사용합니다.
Environmental Standards:
SPFAvailable Region:
GlobalSource:
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