Establishment of feline embryonic stem cells from the inner cell mass of blastocysts produced in vitro

被引:1
|
作者
Yoshida, Takumi [1 ]
Tsukamoto, Masaya [1 ]
Kimura, Kazuto [1 ]
Tanaka, Miyuu [2 ]
Kuwamura, Mitsuru [2 ]
Hatoya, Shingo [1 ]
机构
[1] Osaka Metropolitan Univ, Grad Sch Vet Sci, Dept Adv Pathobiol, Izumisano, Osaka 5988531, Japan
[2] Osaka Metropolitan Univ, Grad Sch Vet Sci, Dept Integrated Struct Biosci, Izumisano, Osaka 5988531, Japan
来源
REGENERATIVE THERAPY | 2025年 / 28卷
关键词
Feline; Embryonic stem cell; Pluripotency; Veterinary regenerative medicine; Artificial reproductive technology; Wildlife conservation; PRESERVATION; DERIVATION; CULTURE; LINE;
D O I
10.1016/j.reth.2024.11.010
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Introduction: The rising number of cats as pets and the growing interest in animal welfare have led to an increased need for the latest treatments in feline veterinary medicine. Among these, veterinary regenerative medicine using pluripotent stem cells is gaining significant attention. However, there have been no reports on establishing feline embryonic stem cell (ESC) lines that possess the pluripotent potential and the ability to differentiate into three germ layers. Methods: In this study, we isolated three inner cell masses from feline in vitro-derived blastocysts and subcultured them in a chemically defined medium (StemFit AK02N). We assessed the expression of undifferentiated markers, the ability to differentiate into the three germ layers, and the karyotype structure. Results: We established three feline ESC lines. Feline ESCs exhibited positive staining for alkaline phosphatase. RT-qPCR analysis revealed that these cells express undifferentiated marker genes in vitro. Immunostaining and flow cytometry analysis demonstrated that feline ESCs express undifferentiated marker proteins in vitro. In the KSR/FBS medium with or without Activin A, feline ESCs differentiated into all three germ layers (ectoderm, endoderm, and mesoderm), expressing specific marker genes and proteins for each germ layer, as evidenced by RT-qPCR, immunostaining, and flow cytometry. Furthermore, we confirmed that feline ESCs formed teratomas comprising all three germ layers in mouse testes, demonstrating de novo pluripotency in vivo. We also verified that the feline ESCs maintained a normal karyotype. Conclusions: We successfully established three feline ESC lines, each possessing pluripotent potential and capable of differentiating into all three germ layers, derived from the inner cell masses of blastocysts produced in vitro. (c) 2024 The Author(s). Published by Elsevier BV on behalf of The Japanese Society for Regenerative Medicine. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/lice nses/by-nc-nd/4.0/).
引用
收藏
页码:63 / 72
页数:10
相关论文
共 50 条
  • [31] Generation of embryonic stem cells: limitations of and alternatives to inner cell mass harvest
    Das, Sunit
    Bonaguidi, Michael
    Muro, Kenji
    Kessler, John A.
    NEUROSURGICAL FOCUS, 2008, 24 (3-4)
  • [32] Induction of T cell development and establishment of T cell competence from embryonic stem cells differentiated in vitro
    Thomas M Schmitt
    Renée F de Pooter
    Matthew A Gronski
    Sarah K Cho
    Pamela S Ohashi
    Juan Carlos Zúñiga-Pflücker
    Nature Immunology, 2004, 5 : 410 - 417
  • [33] Transition of inner cell mass to embryonic stem cells: mechanisms, facts, and hypotheses
    Hassani, Seyedeh-Nafiseh
    Moradi, Sharif
    Taleahmad, Sara
    Braun, Thomas
    Baharvand, Hossein
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2019, 76 (05) : 873 - 892
  • [34] Induction of T cell development and establishment of T cell competence from embryonic stem cells differentiated in vitro
    Schmitt, TM
    de Pooter, RF
    Gronski, MA
    Cho, SK
    Ohashi, PS
    Zúñiga-Pflücker, JC
    NATURE IMMUNOLOGY, 2004, 5 (04) : 410 - 417
  • [35] Oct4 expression in in-vitro-produced sheep blastocysts and embryonic-stem-like cells
    Sanna, Daniela
    Sanna, Angela
    Mara, Laura
    Pilichi, Susanna
    Mastinu, Andrea
    Chessa, Fabrizio
    Pani, Luca
    Dattena, Maria
    CELL BIOLOGY INTERNATIONAL, 2010, 34 (01) : 53 - 60
  • [36] Establishment of novel embryonic stem(ES) cell lines from OG2/rtTA blastocysts
    Hui Yao~(a
    遗传学报, 2011, 38 (07) : 289 - 295
  • [37] Establishment of novel embryonic stem (ES) cell lines from OG2/rtTA blastocysts
    Yao, Hui
    Jiang, Yonghua
    Zhang, Yu
    Liu, Wenqiang
    Huang, Bo
    Wang, Xiaodong
    Gao, Shaorong
    JOURNAL OF GENETICS AND GENOMICS, 2011, 38 (07) : 289 - 295
  • [38] Establishment of embryonic stem cell lines derived from in vitro-produced buffalo (Bubalus bubalis) emibryos.
    Verma, Vinod
    Gautam, Sanjeev
    Chauhan, Man-Mohansingh
    Manik, Radheyshyam
    Palta, Prabliat
    Singla, Sureshkumar
    BIOLOGY OF REPRODUCTION, 2007, : 186 - 187
  • [39] Epigenetic Differences between Embryonic Stem Cells Generated from Blastocysts Developed In Vitro and In Vivo
    Horii, Takuro
    Yanagisawa, Eikichi
    Kimura, Mika
    Morita, Sumiyo
    Hatada, Izuho
    CELLULAR REPROGRAMMING, 2010, 12 (05) : 551 - 563
  • [40] Adjuvant cell culture is required for deriving embryonic stem cells from individually biopsied inner cell mass cells.
    Takeuchi, T.
    Neri, Q. V.
    Seriola, A.
    Cheng, M.
    Palermo, G. D.
    FERTILITY AND STERILITY, 2007, 88 : S43 - S43