Back

Derivation of primed sheep embryonic stem cells and conversion to an intermediate naive-like state

TS, S.; Vasquez-Hidalgo, M. A.; Pillai, V. V.

2026-01-07 developmental biology
10.1101/2025.11.22.689923 bioRxiv
Show abstract

Embryonic stem cells (ESCs) derived from the inner cell mass of embryos possess unlimited self-renewal and pluripotency, offering a powerful system to study early development and enable genetic and biotechnological innovation. Although several livestock ESC lines have been reported in recent years, defining culture conditions that support stable long-term self-renewal and controlled transitions across pluripotent states remains challenging. Here, we report the de novo derivation of sheep embryonic stem cells (sESCs) from in vivo blastocysts using a chemically defined culture system. The derived cells exhibit morphological and molecular features of primed pluripotency and can be propagated under both feeder-dependent and feeder-free conditions without loss of identity or karyotypic stability. Building on this foundation, we developed enhancer-driven reporter lines that faithfully reflect OCT4 and SOX2 transcriptional activity, enabling dynamic visualization of pluripotency and differentiation in live cultures. These reporter systems revealed the responsiveness of sESCs to signaling modulation and provided a functional readout of pluripotency state transitions. When cultured in defined media previously shown to stabilize naive pluripotency in human ESCs, sESCs adopted dome-shaped colony morphology, maintained OCT4, SOX2, and NANOG expression, retained differentiation potential, and exhibited a transcriptomic profile consistent with resetting to an intermediate pluripotent state with naive-like morphological features. These findings establish stable sheep ESC lines and demonstrate their plasticity across the pluripotency spectrum, providing a valuable platform for investigating ruminant stem cell biology and advancing livestock biotechnology.

Matching journals

The top 5 journals account for 50% of the predicted probability mass.

1
Stem Cell Reports
118 papers in training set
Top 0.1%
22.7%
2
Nature Communications
4913 papers in training set
Top 16%
10.5%
3
Frontiers in Cell and Developmental Biology
218 papers in training set
Top 0.3%
8.5%
4
Cell Reports Methods
141 papers in training set
Top 0.5%
4.9%
5
Stem Cells
28 papers in training set
Top 0.1%
4.9%
50% of probability mass above
6
Scientific Reports
3102 papers in training set
Top 23%
4.9%
7
Development
440 papers in training set
Top 0.7%
3.6%
8
Cell Stem Cell
57 papers in training set
Top 0.5%
3.6%
9
Developmental Cell
168 papers in training set
Top 5%
3.6%
10
Communications Biology
886 papers in training set
Top 4%
2.5%
11
Cell Reports
1338 papers in training set
Top 20%
2.4%
12
Advanced Science
249 papers in training set
Top 9%
1.9%
13
PLOS ONE
4510 papers in training set
Top 53%
1.7%
14
iScience
1063 papers in training set
Top 14%
1.7%
15
Nucleic Acids Research
1128 papers in training set
Top 13%
1.2%
16
BMC Biology
248 papers in training set
Top 3%
0.9%
17
Biology Open
130 papers in training set
Top 2%
0.9%
18
The FASEB Journal
175 papers in training set
Top 2%
0.9%
19
Cytometry Part A
30 papers in training set
Top 0.3%
0.8%
20
eLife
5422 papers in training set
Top 57%
0.8%
21
EMBO Molecular Medicine
85 papers in training set
Top 5%
0.7%
22
Science Advances
1098 papers in training set
Top 33%
0.6%
23
Stem Cell Research & Therapy
30 papers in training set
Top 1.0%
0.6%
24
Open Biology
95 papers in training set
Top 3%
0.5%
25
Molecular Therapy
71 papers in training set
Top 4%
0.5%