Xeno-free generation of human induced pluripotent stem cells from donor-matched fibroblasts isolated from dermal and oral tissues

• Published in: Stem cell research & therapy Vol. 14; no. 1; p. 199
• Main Authors: Ali, Hassan R W, Suliman, Salwa, Osman, Tarig Al-Hadi, Carrasco, Manuel, Bruland, Ove, Costea, Daniela-Elena, Ræder, Helge, Mustafa, Kamal
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 09-08-2023; BioMed Central; BMC
• Subjects: Biotechnology industry; Cell culture; Cell differentiation; Chromosomes; Ectoderm; Endoderm; Fetal bovine serum; Fetal calf serum; Fibroblasts; Genomes; Genomics; Genotypes; Good Manufacturing Practice; Growth factors; Mesoderm; Morphology; Oct-4 protein; Pax6 protein; Penicillin; Phenotypes; Plasmids; Platelet lysate; Platelets; Pluripotency; Regenerative medicine; Skin; Somatic cells; Stem cell transplantation; Stem cells; Transcription factors; Transfection; Xenogenic; United States; Canada; Netherlands; United States > US; Massachusetts; Fibroblasts; Platelet lysate; Xenogenic; Fetal bovine serum; Pluripotency
• ISSN: 1757-6512; 1757-6512
• DOI: 10.1186/s13287-023-03403-7

Induced pluripotent stem cells (iPS) can be generated from various somatic cells and can subsequently be differentiated to multiple cell types of the body. This makes them highly promising for cellular therapy in regenerative medicine. However, to facilitate their clinical use and to ensure safety, iPS culturing protocols must be compliant with good manufacturing practice guidelines and devoid of xenogenic products. Therefore, we aimed to compare the efficiency of using humanized culture conditions, specifically human platelet lysate to fetal bovine serum, for iPS generation from different sources, and to evaluate their stemness.
iPS were generated via a platelet lysate or fetal bovine serum-based culturing protocol from matched dermal, buccal and gingival human fibroblasts, isolated from healthy donors (n = 2) after informed consent, via episomal plasmid transfection. Pluripotency, genotype and phenotype of iPS, generated by both protocols, were then assessed by various methods.
More attempts were generally required to successfully reprogram xeno-free fibroblasts to iPS, as compared to xenogenic cultured fibroblasts. Furthermore, oral fibroblasts generally required more attempts for successful iPS generation as opposed to dermal fibroblasts. Morphologically, all iPS generated from fibroblasts formed tight colonies surrounded by a reflective "whitish" outer rim, typical for iPS. They also expressed pluripotency markers at both gene (SOX2, OCT4, NANOG) and protein level (SOX2, OCT4). Upon stimulation, all iPS showed ability to differentiate into the three primary germ layers via expression of lineage-specific markers for mesoderm (MESP1, OSR1, HOPX), endoderm (GATA4) and ectoderm (PAX6, RAX). Genome analysis revealed several amplifications and deletions within the chromosomes of each iPS type.
The xeno-free protocol had a lower reprogramming efficiency compared to the standard xenogenic protocol. The oral fibroblasts generally proved to be more difficult to reprogram than dermal fibroblasts. Xeno-free dermal, buccal and gingival fibroblasts can successfully generate iPS with a comparable genotype/phenotype to their xenogenic counterparts.