Inpp5d-KO Mouse
Common Name
Inpp5d-KO
제품 ID
S-KO-16385
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-16331-Inpp5d-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Inpp5d-KO Mouse (카탈로그 번호 S-KO-16385)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
Inpp5d-KO
품종 계통계통 ID
KOCMP-16331-Inpp5d-B6J-VA
유전자명
제품 ID
S-KO-16385
유전자 별칭
SHIP, SHIP1, SHIP-1, s-SHIP, SIP-145, p150Ship
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 1
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000169754
NCBI 전사체 ID
NM_010566
타겟 영역
Exon 10~17
유효 영역 크기
~11.6 kb
유전자 연구 개요
Inpp5d, also known as Inositol polyphosphate-5-phosphatase D, encodes a dual-specificity phosphatase that can dephosphorylate both phospholipids and phosphoproteins. It is a myeloid-expressed gene, and its protein product SHIP1 is an important regulator in microglial phagocytosis, immune response, and phosphoinositide signaling. The NLRP3 inflammasome signaling is one of the associated pathways, and Inpp5d is genetically associated with Alzheimer's disease (AD), highlighting its significance in neurodegenerative disease research [1,2,3,4,5,6,7,8,9,10].
In Inpp5d-deficient mouse models, several important findings have emerged. In the PSAPP mouse model, conditional Inpp5d down-regulation increased plaque burden and the recruitment of microglia to plaques [2]. In the 5xFAD mouse model, Inpp5d haplodeficiency enhanced microglial functions by increasing plaque clearance and preserved cognitive abilities [6]. In the PS19 mouse model of Tauopathy, Inpp5d haplodeficiency alleviated tau pathology and motor deficits [7]. Also, loss of Inpp5d in wild-type mice had sex-specific effects on the brain transcriptome, with affected genes enriched for multiple neurodegeneration terms [8]. In 5xFAD Inpp5dfl/fl Cx3cr1Ert2Cre mice, SHIP-1 deletion in microglia led to enhanced microglial recruitment to Aβ plaques, improved neuronal health, and enhanced plaque containment and Aβ engulfment [10].
In conclusion, Inpp5d is a crucial regulator in microglial-mediated processes, especially in the context of AD-related pathology. Mouse models, including KO/CKO models, have been instrumental in revealing its role in plaque formation, microglial function, and cognitive preservation in AD, as well as in tau pathology. These findings offer potential therapeutic strategies targeting Inpp5d for neurodegenerative diseases.
References:
1. Chou, Vicky, Pearse, Richard V, Aylward, Aimee J, Menon, Vilas, Young-Pearse, Tracy L. 2023. INPP5D regulates inflammasome activation in human microglia. In Nature communications, 14, 7552. doi:10.1038/s41467-023-42819-w. https://pubmed.ncbi.nlm.nih.gov/38016942/
2. Castranio, Emilie L, Hasel, Philip, Haure-Mirande, Jean-Vianney, Liddelow, Shane A, Ehrlich, Michelle E. 2022. Microglial INPP5D limits plaque formation and glial reactivity in the PSAPP mouse model of Alzheimer's disease. In Alzheimer's & dementia : the journal of the Alzheimer's Association, 19, 2239-2252. doi:10.1002/alz.12821. https://pubmed.ncbi.nlm.nih.gov/36448627/
3. Terzioglu, Gizem, Young-Pearse, Tracy L. 2023. Microglial function, INPP5D/SHIP1 signaling, and NLRP3 inflammasome activation: implications for Alzheimer's disease. In Molecular neurodegeneration, 18, 89. doi:10.1186/s13024-023-00674-9. https://pubmed.ncbi.nlm.nih.gov/38017562/
4. Olufunmilayo, Edward O, Holsinger, R M Damian. 2023. INPP5D/SHIP1: Expression, Regulation and Roles in Alzheimer's Disease Pathophysiology. In Genes, 14, . doi:10.3390/genes14101845. https://pubmed.ncbi.nlm.nih.gov/37895194/
5. Chou, Vicky, Fancher, Seeley B, Pearse, Richard V, Menon, Vilas, Young-Pearse, Tracy L. 2023. INPP5D/SHIP1 regulates inflammasome activation in human microglia. In bioRxiv : the preprint server for biology, , . doi:10.1101/2023.02.25.530025. https://pubmed.ncbi.nlm.nih.gov/36865139/
6. Lin, Peter Bor-Chian, Tsai, Andy Po-Yi, Soni, Disha, Lamb, Bruce T, Oblak, Adrian L. 2022. INPP5D deficiency attenuates amyloid pathology in a mouse model of Alzheimer's disease. In Alzheimer's & dementia : the journal of the Alzheimer's Association, 19, 2528-2537. doi:10.1002/alz.12849. https://pubmed.ncbi.nlm.nih.gov/36524682/
7. Soni, Disha M, Lin, Peter Bor-Chian, Lee-Gosselin, Audrey, Chu, Shaoyou, Oblak, Adrian L. 2024. Inpp5d haplodeficiency alleviates tau pathology in the PS19 mouse model of Tauopathy. In Alzheimer's & dementia : the journal of the Alzheimer's Association, 20, 4985-4998. doi:10.1002/alz.14078. https://pubmed.ncbi.nlm.nih.gov/38923171/
8. Dabin, Luke C, Kersey, Holly, Kim, Byungwook, Lamb, Bruce T, Kim, Jungsu. 2024. Loss of Inpp5d has disease-relevant and sex-specific effects on glial transcriptomes. In Alzheimer's & dementia : the journal of the Alzheimer's Association, 20, 5311-5323. doi:10.1002/alz.13901. https://pubmed.ncbi.nlm.nih.gov/38923164/
9. Karch, Celeste M, Goate, Alison M. 2014. Alzheimer's disease risk genes and mechanisms of disease pathogenesis. In Biological psychiatry, 77, 43-51. doi:10.1016/j.biopsych.2014.05.006. https://pubmed.ncbi.nlm.nih.gov/24951455/
10. Samuels, Joshua D, Moore, Katelyn A, Ennerfelt, Hannah E, Price, Richard J, Lukens, John R. 2023. The Alzheimer's disease risk factor INPP5D restricts neuroprotective microglial responses in amyloid beta-mediated pathology. In Alzheimer's & dementia : the journal of the Alzheimer's Association, 19, 4908-4921. doi:10.1002/alz.13089. https://pubmed.ncbi.nlm.nih.gov/37061460/
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:
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