Ptgds-KO Mouse
Common Name
Ptgds-KO
제품 ID
S-KO-18883
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-19215-Ptgds-B6J-VB
상태
이 마우스 계통을 논문에서 사용할 경우, “Ptgds-KO Mouse (카탈로그 번호 S-KO-18883)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
Ptgds-KO
품종 계통계통 ID
KOCMP-19215-Ptgds-B6J-VB
유전자명
제품 ID
S-KO-18883
유전자 별칭
PGD2, PGDS, 21kDa, PGDS2, Ptgs3, L-PGDS
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 2
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000015234
NCBI 전사체 ID
NM_008963
타겟 영역
Exon 2~3
유효 영역 크기
~0.3 kb
유전자 연구 개요
Ptgds, or prostaglandin D2 synthase, is a glycoprotein belonging to the lipocalin superfamily. It plays dual roles in prostaglandins metabolism and lipid transport, and is involved in various cellular processes [1,2]. It may be associated with pathways like Wnt-β-catenin-STAT3, and has significance in biological processes related to cell proliferation, apoptosis, and cell cycle regulation [1].
In multiple cancers, its role has been explored. In diffuse large B-cell lymphoma (DLBCL), high Ptgds expression correlated with poor prognosis, and its knockdown or treatment with inhibitor AT56 exerted anti-tumor effects by regulating cell functions and enhancing drug sensitivity, possibly through MYH9-mediated regulation of Wnt-β-catenin-STAT3 signaling [1]. In peripheral T cell lymphoma (PTCL), high Ptgds expression was linked to poor prognosis, and its knockdown and AT56 treatment inhibited PTCL progression and promoted ferroptosis by regulating HMOX1-mediated iron metabolism [3]. In cervical squamous cell carcinoma, PTGDS showed low expression, and it was an independent prognostic indicator [4]. In medulloblastoma, low PTGDS expression was associated with a lower 3-year survival rate [5]. In endometrial cancer, decreased PTGDS expression predicted poor survival, and it may be involved in the adaptive immune response, leukocyte migration, and regulation of cell adhesion molecules and chemokine signaling [6]. In prostate adenocarcinoma, overexpression of PTGDS suppressed cell migration, invasion, and proliferation [7]. Also, in aminoglycoside-induced vestibular dysfunction, Ptgds knockdown protected vestibular hair cells [2]. In a Parkinson's disease mouse model, MLKL deficiency led to downregulated Ptgds expression, reduced microglial cells, and dampened neuron death [8]. In rosacea, knockdown of Ptgds in fibroblasts blocked rosacea development in mice [9].
In summary, Ptgds is involved in diverse biological processes with implications in multiple disease areas. Gene knockdown and inhibitor studies, similar to those in KO mouse models, have revealed its roles in cancer progression, vestibular hair cell protection, and neurodegenerative disease-related inflammation. Understanding Ptgds can potentially offer new therapeutic strategies for these diseases.
References:
1. Hu, Shunfeng, Ren, Shuai, Cai, Yiqing, Zhou, Xiangxiang, Wang, Xin. 2021. Glycoprotein PTGDS promotes tumorigenesis of diffuse large B-cell lymphoma by MYH9-mediated regulation of Wnt-β-catenin-STAT3 signaling. In Cell death and differentiation, 29, 642-656. doi:10.1038/s41418-021-00880-2. https://pubmed.ncbi.nlm.nih.gov/34743203/
2. Chen, Chen, Zhao, Zhimin, Han, Jinghong, Zhang, Yue, Nie, Guohui. 2025. Ptgds downregulation protect vestibular hair cells from aminoglycoside-induced vestibulotoxicity. In PloS one, 20, e0320634. doi:10.1371/journal.pone.0320634. https://pubmed.ncbi.nlm.nih.gov/40198625/
3. Hu, Shunfeng, Liu, Bingyu, Shang, Juanjuan, Zhou, Xiangxiang, Wang, Xin. 2024. Targeting PTGDS Promotes ferroptosis in peripheral T cell lymphoma through regulating HMOX1-mediated iron metabolism. In British journal of cancer, 132, 384-400. doi:10.1038/s41416-024-02919-w. https://pubmed.ncbi.nlm.nih.gov/39706989/
4. Jiang, Pinping, Cao, Ying, Gao, Feng, Xie, Manxin, Fu, Shilong. 2021. SNX10 and PTGDS are associated with the progression and prognosis of cervical squamous cell carcinoma. In BMC cancer, 21, 694. doi:10.1186/s12885-021-08212-w. https://pubmed.ncbi.nlm.nih.gov/34116656/
5. Ren, Zhangping, Gao, Ming, Jiang, Wei. 2022. Prognostic role of NLGN2 and PTGDS in medulloblastoma based on gene expression omnibus. In American journal of translational research, 14, 3769-3782. doi:. https://pubmed.ncbi.nlm.nih.gov/35836891/
6. Zou, Ruoyao, Zheng, Mingjun, Tan, Mingzi, Luan, Nannan, Zhu, Liancheng. 2020. Decreased PTGDS Expression Predicting Poor Survival of Endometrial Cancer by Integrating Weighted Gene Co-Expression Network Analysis and Immunohistochemical Validation. In Cancer management and research, 12, 5057-5075. doi:10.2147/CMAR.S255753. https://pubmed.ncbi.nlm.nih.gov/32617019/
7. Chen, Bohong, Guo, Li, Wang, Lihui, Wu, Dapeng, Du, Yuefeng. 2024. Leveraging cell death patterns to predict metastasis in prostate adenocarcinoma and targeting PTGDS for tumor suppression. In Scientific reports, 14, 21680. doi:10.1038/s41598-024-72985-w. https://pubmed.ncbi.nlm.nih.gov/39289451/
8. Geng, Lu, Gao, Wenqing, Saiyin, Hexige, Zhang, Zhuohua, Li, Jixi. 2023. MLKL deficiency alleviates neuroinflammation and motor deficits in the α-synuclein transgenic mouse model of Parkinson's disease. In Molecular neurodegeneration, 18, 94. doi:10.1186/s13024-023-00686-5. https://pubmed.ncbi.nlm.nih.gov/38041169/
9. Chen, Mengting, Yang, Li, Zhou, Peijie, Deng, Zhili, Li, Ji. 2024. Single-cell transcriptomics reveals aberrant skin-resident cell populations and identifies fibroblasts as a determinant in rosacea. In Nature communications, 15, 8737. doi:10.1038/s41467-024-52946-7. https://pubmed.ncbi.nlm.nih.gov/39384741/
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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