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Adipoq-iCre Mouse
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Adipoq-iCre Mouse
製品名
Adipoq-iCre Mouse
製品ID
C001529
系統名
C57BL/6JCya-Adipoqem1(P2A-iCre)/Cya
背景情報
C57BL/6JCya
組織や細胞を表現する例
Adipocytes
状況
このマウス系統を論文で使用する場合は、「Adipoq-iCre Mouse(カタログ番号C001529)はサイアジェンから購入しました。」と引用してください。
Cre Mouse Models
製品タイプ
年齢
遺伝子型
性別
数量
標準的な配送方法では、少なくとも3匹のヘテロ接合体キャリアを保証しています。ホモ接合体キャリアや指定された性別の個体の繁殖サービスも利用可能です。
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Cre Mouse Models
基本情報
検証 Data
関連リソース
基本情報
遺伝子名
遺伝子別名
Ad, APN, Acdc, Adid, apM1, 30kDa, GBP28, adipo, Acrp30
NCBI ID
染色体
Chr 16
MGI ID
さらに
系統詳細
The ADIPOQ gene-encoded adiponectin is a protein hormone produced exclusively by adipocytes (fat cells). It is transported through the bloodstream to muscle and liver cells. Adiponectin regulates various pathways related to fat storage and metabolism, including the modulation of blood glucose levels, fatty acid breakdown, brown adipocyte differentiation, and negative regulation of gluconeogenesis. By increasing insulin sensitivity and promoting fatty acid breakdown, adiponectin plays a crucial role in regulating glucose and fat metabolism. Additionally, it exhibits direct anti-diabetic, anti-atherosclerotic, and anti-inflammatory activities [1-2]. The mutation of the ADIPOQ gene is associated with adiponectin deficiency syndrome. Although the ADIPOQ gene is expressed predominantly (or almost exclusively) in adipose tissue, adiponectin, as a secreted hormone, circulates via the bloodstream and is widely distributed in various tissues and organs, including skeletal muscle, liver, intestine, male reproductive glands, and brain, where it exerts its physiological effects through specific receptors (such as AdipoR1 and AdipoR2) [3-4].
The Adipoq-iCre mice are constructed by inserting a codon-improved Cre recombinase (iCre) element into the endogenous Adipoq gene of mice. The expression pattern of iCre recombinase is similar to the endogenous gene. When this strain is crossed with mice containing loxP sites, sequence recombination mediated by the Cre recombinase between loxP sites can occur in the white adipose tissue (WAT) and brown adipose tissue (BAT) of its offspring.
参考文献
Maeda K, Okubo K, Shimomura I, Funahashi T, Matsuzawa Y, Matsubara K. cDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (AdiPose Most abundant Gene transcript 1). Biochem Biophys Res Commun. 1996 Apr 16;221(2):286-9.
Martinez-Huenchullan SF, Tam CS, Ban LA, Ehrenfeld-Slater P, Mclennan SV, Twigg SM. Skeletal muscle adiponectin induction in obesity and exercise. Metabolism. 2020 Jan;102:154008.
Oliveira CS, Giuffrida FM, Crispim F, Saddi-Rosa P, Reis AF. ADIPOQ and adiponectin: the common ground of hyperglycemia and coronary artery disease? Arq Bras Endocrinol Metabol. 2011 Oct;55(7):446-54.
Spranger J, Verma S, Göhring I, Bobbert T, Seifert J, Sindler AL, Pfeiffer A, Hileman SM, Tschöp M, Banks WA. Adiponectin does not cross the blood-brain barrier but modifies cytokine expression of brain endothelial cells. Diabetes. 2006 Jan;55(1):141-7.
系統作製戦略
The stop codon was replaced with the P2A-iCre cassette.

Figure 1. Diagram of the gene editing strategy for the generation of Adipoq-iCre mice.
検証 Data
1. Method
Adipoq-iCre mice were mated with Rosa26-LSL-tdTomato mice to generate double heterozygotes. Deletion of the “stop element (LSL)” results in tdTomato protein expression in Cre-positive cells. When the offspring mice reach 6 weeks of age, mouse white adipose tissue, brown adipose tissue, skeletal muscle, skin, lungs, heart, testicles, and ovarian tissues are collected and tdTomato protein distribution is analyzed by immunofluorescence (IF) to determine the expression of Cre recombinase.
2. Genotype
Cre+: Adipoq-iCre[KI/+];Rosa26-LSL-tdTomato[CKI/+];
Cre-: Rosa26-LSL-tdTomato[CKI/CKI].
3. Result
(1)Expression of Cre recombinase in white adipose tissue and brown adipose tissue
The results reveal that in Cre+ mice, there is abundant red fluorescence from tdTomato in the adipocytes, indicating tdTomato expression mediated by Cre recombinase in these cells. Conversely, in Cre- mice, there is no activity of Cre recombinase in both white and brown adipose tissues.

Figure 2. Immunofluorescence (IF) staining of the white adipose tissue (WAT) and brown adipose tissue (BAT).
(2)Expression of Cre recombinase in skeletal muscle and skin
The results indicate that in Cre+ mice, there is a partial red fluorescence signal present in the adipocytes adjacent to the skeletal muscle and skin, demonstrating that Cre-mediated recombination has occurred in these cells. Conversely, in Cre- mice, there is no activity of Cre recombinase detected in the skeletal muscle and skin.

Figure 3. Immunofluorescence (IF) staining of the skeletal muscle and skin.
(3)Expression of Cre recombinase in lungs and heart
The results indicate that in Cre+ mice, there is a partial fluorescence signal present in the adipocytes of the lungs and bronchi, while extremely low levels of fluorescence signal are observed in the heart. Conversely, in Cre- mice, there is no activity of Cre recombinase detected in both the lungs and heart.

Figure 4. Immunofluorescence (IF) staining of the lungs and heart.
(4)Expression of Cre recombinase in testicles and ovaries
The results indicate that in Cre+ mice, there is no observed red fluorescence signal in the testicles. However, in the ovarian perifollicular fat, ovarian stroma, and corpus luteum of Cre+ mice, there is a small amount of fluorescence signal, indicating tdTomato expression mediated by Cre recombinase in these cells. Conversely, in Cre- mice, there is no activity of Cre recombinase detected in both the testicles and ovaries.

Figure 5. Immunofluorescence (IF) staining of the testicles and ovaries.
4. Summary
In Adipoq-iCre mice, the expression of Cre recombinase is primarily concentrated in white adipose tissue (WAT) and brown adipose tissue (BAT). Additionally, there are partial recombination signals observed in the skeletal muscle, skin, lungs, and heart of mice. Based on histological assessment, these cell types in the mentioned tissues are likely adipocytes. Overall, this model can be utilized for tissue-specific research targeting adipose tissue.
関連リソース
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