# A practical approach for the stable isolation and cultivation of chicken gonadal primordial germ cells with mitotically inactivated STO feeder cells

**Authors:** Hyeon Yang, Bo Ram Lee, Jae-Yeong Lee, Keon Bong Oh, Poongyeon Lee, Seunghoon Lee, Yong Jin Jo, Haesun Lee, Seokho Kim, Jingu No, Jae Yong Han, Sung June Byun

PMC · DOI: 10.5713/ab.25.0192 · 2025-06-04

## TL;DR

This paper presents a reliable method to isolate and grow chicken germ cells in the lab, which is important for creating genetically modified chickens.

## Contribution

A practical and stable method for culturing chicken primordial germ cells using mitotically inactivated STO feeder cells is introduced.

## Key findings

- PGCs proliferated robustly, reaching over 10⁵ cells within one month.
- Expression of PGC-specific markers and pluripotency genes was confirmed.
- Injected PGCs successfully migrated to recipient embryonic gonads.

## Abstract

Establishing chicken primordial germ cells (PGCs) in vitro is critical for producing genetically modified (GM) chickens. Efficient and reliable isolation and cultivation of PGCs remain significant challenges in advancing avian genetic modifications. To address these challenges, we employed a streamlined and practical approach for the efficient isolation and stable cultivation of chicken gonadal PGCs.

Chicken gonadal PGCs were isolated from embryonic gonads, surgically removed and dissociated using trypsin. The PGCs were isolated by exploiting differential adhesion properties, allowing fibroblasts to attach while PGCs remained suspended. Cultivation was performed with mitotically inactivated SIM mouse embryo-derived thioguanine-resistant (STO) feeder cells under optimized culture conditions.

PGCs proliferated robustly, reaching over 105 cells within one month, which is comparable to previously reported methods. Characterization assays confirmed the expression of PGC-specific markers, including SSEA-1 and DAZL, along with pluripotency-related genes such as OCT4 and NANOG. Additionally, injected PGCs successfully migrated to recipient embryonic gonads, where their presence was confirmed by fluorescence analysis and PCR.

This study highlights the effectiveness of the STO feeder-based culture system in avian germ cell research, contributing to progress in the production of germline chimeric and GM chickens.

## Linked entities

- **Genes:** FUT4 (fucosyltransferase 4) [NCBI Gene 2526], DAZL (deleted in azoospermia like) [NCBI Gene 1618], POU5F1 (POU class 5 homeobox 1) [NCBI Gene 5460], NANOG (Nanog homeobox) [NCBI Gene 79923]
- **Chemicals:** thioguanine (PubChem CID 2723601)
- **Species:** Gallus gallus (taxon 9031), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** DAZL (deleted in azoospermia like) [NCBI Gene 374054], NANOG (Nanog homeobox) [NCBI Gene 100272166]
- **Species:** Gallus gallus (bantam, species) [taxon 9031]
- **Cell lines:** STO — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_3420)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12580769/full.md

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Source: https://tomesphere.com/paper/PMC12580769