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Updated: Dec 30, 2025

Reprogramming Primary Amniotic Fluid and Membrane Cells to Pluripotency in Xeno-free Conditions
Published on: November 27, 2017
Generation and characterization of a human iPSC line derived from congenital clubfoot amniotic fluid cells
Jing Wang1, Yazhou Cui2, Kaixuan Xing2
1School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Ji'nan, Shandong, China; Shandong Medicinal Biotechnology Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Ji'nan, Shandong, China; Key Laboratory for Biotech-Drugs of National Health Commission, Ji'nan, Shandong, China.
Insights
A new human induced pluripotent stem cell line was created from amniotic fluid cells of a fetus with clubfoot. This cellular model offers a valuable resource for investigating clubfoot pathology.
Area of Science:
- Stem cell biology
- Developmental biology
- Genetics
Background:
- Clubfoot etiology remains unclear, hindering effective treatment development.
- Human induced pluripotent stem cells (iPSCs) offer a promising in vitro model for studying congenital disorders.
- Amniotic fluid-derived cells (AFDCs) are a viable source for iPSC generation.
Observation:
- A novel human induced pluripotent stem cell (iPSC) line, SMBCi002-A, was successfully generated from amniocytes.
- The iPSC line was derived from a female fetus diagnosed with clubfoot.
- A non-integrative episomal plasmid strategy was employed for cell reprogramming, utilizing factors OCT4, SOX2, KLF4, MYC, LIN28, and EBNA1.
Findings:
- Comprehensive validation assays confirmed the pluripotency of the SMBCi002-A iPSC line.
- The established iPSC line demonstrated robust differentiation potential across multiple lineages.
- Genetic stability assessments indicated the integrity of the reprogrammed cells.
Implications:
- The SMBCi002-A iPSC line serves as a critical in vitro model for clubfoot research.
- This cellular resource facilitates the investigation of clubfoot's underlying mechanisms and pathology.
- Understanding clubfoot pathogenesis can pave the way for novel therapeutic strategies.
Abstract:
A human induced pluripotent stem cell (iPSC) line (SMBCi002-A) was established from amniocytes (amniotic fluid cells, AFDCs) from a 16-week-old female fetus with clubfoot. Reprogramming and enhancing factors OCT4, SOX2, KLF4, MYC, LIN28 and EBNA1 were delivered using a nonintegrative strategy based on episomal plasmids. Validation assays indicated that this iPSC line has full pluripotency, differentiation potential and genetic stability. Currently, the etiology and mechanism of clubfoot remain unclear; therefore, this in vitro cellular model would provide a useful resource for understanding the pathology of this disease.
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