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Sftpc-MerCreMer Mouse
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Sftpc-MerCreMer Mouse
製品名
Sftpc-MerCreMer Mouse
製品ID
C001501
系統名
C57BL/6JCya-Sftpcem2(IRES-MerCreMer)/Cya
背景情報
C57BL/6JCya
状況
このマウス系統を論文で使用する場合は、「Sftpc-MerCreMer Mouse(カタログ番号C001501)はサイアジェンから購入しました。」と引用してください。
Inducible 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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Inducible 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
SP5, SPC, SP-C, Sftp2, Bricd6, Sftp-2, pro-SpC
NCBI ID
染色体
Chr 14
MGI ID
さらに
系統詳細
The SFTPC gene encodes surfactant protein C (SP-C), one of the four key proteins in surfactant. Surfactant is a mixture of lipids and proteins that coats the lung tissue, making breathing easier. Surfactant is secreted by alveolar cells and maintains the stability of the lung tissue by reducing the surface tension of the fluid that covers the lung. In addition, SP-C is involved in lung development and function, including alveolar septation, airway remodeling, and immune defense. The SFTPC gene is primarily expressed in the lung, with the highest expression in the lower lobe, right lung, upper lobe, left upper lobe, and visceral pleura. It is also expressed at low levels in other tissues. Type II alveolar cells are responsible for the production and secretion of surfactants. Therefore, the SFTPC gene is primarily expressed in these cells and can be used as a specific marker for these cells.
Sftpc-MerCreMer mice were generated to integrate the tamoxifen-inducible MerCreMer recombinase expression element into the 3’UTR of the mouse Sftpc gene. This mimics the expression pattern of the endogenous gene while maintaining Sftpc expression. When bred with mice carrying a loxP site-flanked sequence, Cre recombinase-mediated recombination of the flanked sequence occurs in type II alveolar cells, following tamoxifen induction.
系統作製戦略
The IRES-MerCreMer gene expression element was integrated into the 3'UTR of the mouse Sftpc gene.

Figure 1. Diagram of the gene editing strategy for the generation of Sftpc-MerCreMer mice.
検証 Data
1. Method
Sftpc-MerCreMer mice were mated with Rosa26-LSL-tdTomato mice to generate double heterozygous zygote mice. Tamoxifen induction (4 mg/mouse for 4 days, i.p.) was performed at 6 weeks of age, resulting in Cre recombinase-mediated deletion of the LSL elements and subsequent expression of tdTomato in Cre-positive cells. One week after induction, Lung, trachea, and kidney tissue was collected from the offspring, and the distribution of tdTomato was determined by Immunofluorescent staining to assess Cre recombinase expression. The control group received the same dose of corn oil.
2. Groups
Cre+Tam+: Sftpc-MerCreMer[KI/+];Rosa26-LSL-tdTomato[CKI/+], Tamoxifen-induced;
Cre+Tam-: Sftpc-MerCreMer[KI/+];Rosa26-LSL-tdTomato[CKI/+], Corn oil-treated;
3. Result
(1)Expression of Cre recombinase in the lung
Results showed that strong Cre recombinase activity was present in type II alveolar cells of mice induced by tamoxifen (Cre+Tam+). Cre recombinase activity was not detected in the lungs of mice in the non-Tamoxifen-induced group (Cre+Tam-). These results suggest that Cre recombinase activity and specificity in the mouse lung tissue are high, and there is no expression leakage.

Figure 2. Immunofluorescence (IF) staining of lung tissues.
(2)Expression of Cre recombinase in other tissues
Immunofluorescent staining was performed to detect the expression of tdTomato protein in the trachea and kidney tissue of mice. Results showed that Cre recombinase activity was present in a subset of tracheal cells of mice induced by tamoxifen (Cre+Tam+), but not in the kidney. Cre recombinase activity was not detected in these areas of mice in the non-Tamoxifen-induced group (Cre+Tam-). These results suggest that a small amount of Cre recombinase activity is present in a subset of the tracheal tissue of mice.

Figure 3. Immunofluorescence (IF) staining of trachea and kidney tissue.
4. Summary
In the Sftpc-MerCreMer mouse model, Cre recombinase is predominantly expressed in type II alveolar cells. Overall, the mice do not exhibit pre-induction expression leakage. In conclusion, this model is a highly tissue-specific Cre mouse targeting type II alveolar cells.
関連リソース
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