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Isolation and Culture of Primary Human Mammary Epithelial Cells.
Qian, Linfeng; Yan, Jiaxi; Chen, Shiqi; Abbas Karekad, Maryam Mohanmmed; Wu, Yue; Wu, Xunwei; Xu, Xiaohong; Zhang, Xiaoqun.
Affiliation
  • Qian L; The First Clinical Medical College of Zhejiang Chinese Medical University.
  • Yan J; The First Clinical Medical College of Zhejiang Chinese Medical University.
  • Chen S; The First Clinical Medical College of Zhejiang Chinese Medical University.
  • Abbas Karekad MM; The International Education College of Zhejiang Chinese Medical University.
  • Wu Y; Department of Breast Surgery, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine); Bozhou District Hospital of Traditional Chinese Medicine.
  • Wu X; Engineering Laboratory for Biomaterials and Tissue Regeneration, Ningbo Stomatology Hospital, Ningbo, China and Savaid Stomatology School, Hangzhou Medical College.
  • Xu X; Department of Breast Surgery, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine); Bozhou District Hospital of Traditional Chinese Medicine; 20163329@zcmu.edu.cn.
  • Zhang X; Department of Surgery, Kaihua District, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine); Kaihua County Hospital of Traditional Chinese Medicine; Khzxq333@163.com.
J Vis Exp ; (207)2024 May 03.
Article in En | MEDLINE | ID: mdl-38767371
ABSTRACT
The mammary gland is a fundamental structure of the breast and plays an essential role in reproduction. Human mammary epithelial cells (HMECs), which are the origin cells of breast cancer and other breast-related inflammatory diseases, have garnered considerable attention. However, isolating and culturing primary HMECs in vitro for research purposes has been challenging due to their highly differentiated, keratinized nature and their short lifespan. Therefore, developing a simple and efficient method to isolate and culture HMECs is of great scientific value for the study of breast biology and breast-related diseases. In this study, we successfully isolated primary HMECs from small amounts of mammary tissue by digestion with a mixture of enzymes combined with an initial culture in 5% fetal bovine serum-DMEM containing the Rho-associated kinase (ROCK) inhibitor Y-27632, followed by culture expansion in serum-free keratinocyte medium. This approach selectively promotes the growth of epithelial cells, resulting in an optimized cell yield. The simplicity and convenience of this method make it suitable for both laboratory and clinical research, which should provide valuable insights into these important areas of study.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Culture Techniques / Mammary Glands, Human / Epithelial Cells Limits: Female / Humans Language: En Journal: J Vis Exp Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Culture Techniques / Mammary Glands, Human / Epithelial Cells Limits: Female / Humans Language: En Journal: J Vis Exp Year: 2024 Document type: Article Country of publication: