Giuseppe Di Taranto1, Claudia Cicione2, Giuseppe Visconti3, Maria A Isgrò4, Marta Barba2, Enrico Di Stasio4, Egidio Stigliano5, Camilla Bernardini2, Fabrizio Michetti6, Marzia Salgarello3, Wanda Lattanzi7. 1. Institute of Anatomy and Cell Biology, Università Cattolica del Sacro Cuore, Rome, Italy; Department of Plastic and Reconstructive Surgery, Università Cattolica del Sacro Cuore University Hospital A. Gemelli Rome, Italy. 2. Institute of Anatomy and Cell Biology, Università Cattolica del Sacro Cuore, Rome, Italy. 3. Department of Plastic and Reconstructive Surgery, Università Cattolica del Sacro Cuore University Hospital A. Gemelli Rome, Italy. 4. Institute of Biochemistry and Clinical Biochemistry, Università Cattolica del Sacro Cuore University Hospital A. Gemelli Rome, Italy. 5. Institute of Pathology, Università Cattolica del Sacro Cuore, Rome, Italy. 6. Institute of Anatomy and Cell Biology, Università Cattolica del Sacro Cuore, Rome, Italy; Latium Musculoskeletal Tissue Bank, Rome, Italy. 7. Institute of Anatomy and Cell Biology, Università Cattolica del Sacro Cuore, Rome, Italy; Latium Musculoskeletal Tissue Bank, Rome, Italy. Electronic address: wanda.lattanzi@rm.unicatt.it.
Abstract
BACKGROUND AIMS: Subcutaneous fat represents a valuable reservoir of adipose-derived stem cells (ASCs) in the stromal vascular fraction (SVF), widely exploited in regenerative medicine applications, being easily harvested through lipoaspiration. The lack of standardized procedures for autologous fat grafting guided research efforts aimed at identifying possible differences related to the harvesting site, which may affect cell isolation yield, cell growth properties and clinical outcomes. Subcutaneous fat features a complex architecture: the superficial fascia separates superficial adipose tissue (SAT) from deep layer tissue (DAT). We aimed to unravel the differences between SAT and DAT, considering morphological structure, SVF composition, and ASC properties. METHODS: SAT and DAT were collected from female donors and comparatively analyzed to evaluate cellular yield and viability, morphology, immunophenotype and molecular profile. ASCs were isolated in primary culture and used for in vitro differentiation assays. SAT and DAT from cadaver donors were also analyzed through histology and immunohistochemistry to assess morphology and cell localization within the hypoderm. RESULTS: Liposuctioned SAT contained a higher stromal tissue compound, along with a higher proportion of CD105-positive cells, compared with DAT from the same harvesting site. Also, cells isolated from SAT displayed increased multipotency and stemness features. All differences were mainly evidenced in specimens harvested from the abdominal region. According to our results, SAT features overall increased stem properties. CONCLUSIONS: Given that subcutaneous adipose tissue is currently exploited as the gold standard source for high-yield isolation of adult stem cells, these results may provide precious hints toward the definition of standardized protocols for microharvesting.
BACKGROUND AIMS: Subcutaneous fat represents a valuable reservoir of adipose-derived stem cells (ASCs) in the stromal vascular fraction (SVF), widely exploited in regenerative medicine applications, being easily harvested through lipoaspiration. The lack of standardized procedures for autologous fat grafting guided research efforts aimed at identifying possible differences related to the harvesting site, which may affect cell isolation yield, cell growth properties and clinical outcomes. Subcutaneous fat features a complex architecture: the superficial fascia separates superficial adipose tissue (SAT) from deep layer tissue (DAT). We aimed to unravel the differences between SAT and DAT, considering morphological structure, SVF composition, and ASC properties. METHODS: SAT and DAT were collected from female donors and comparatively analyzed to evaluate cellular yield and viability, morphology, immunophenotype and molecular profile. ASCs were isolated in primary culture and used for in vitro differentiation assays. SAT and DAT from cadaver donors were also analyzed through histology and immunohistochemistry to assess morphology and cell localization within the hypoderm. RESULTS: Liposuctioned SAT contained a higher stromal tissue compound, along with a higher proportion of CD105-positive cells, compared with DAT from the same harvesting site. Also, cells isolated from SAT displayed increased multipotency and stemness features. All differences were mainly evidenced in specimens harvested from the abdominal region. According to our results, SAT features overall increased stem properties. CONCLUSIONS: Given that subcutaneous adipose tissue is currently exploited as the gold standard source for high-yield isolation of adult stem cells, these results may provide precious hints toward the definition of standardized protocols for microharvesting.
Authors: Sarosh Siddiqi; Nattawat Klomjit; Kai Jiang; Sabena M Conley; Xianyang Zhu; Ishran M Saadiq; Christopher M Ferguson; Hui Tang; Amir Lerman; Lilach O Lerman Journal: Stem Cell Rev Rep Date: 2022-09-01 Impact factor: 6.692
Authors: Maria Eugenia Fernández-Santos; Mariano Garcia-Arranz; Enrique J Andreu; Ana Maria García-Hernández; Miriam López-Parra; Eva Villarón; Pilar Sepúlveda; Francisco Fernández-Avilés; Damian García-Olmo; Felipe Prosper; Fermin Sánchez-Guijo; Jose M Moraleda; Agustin G Zapata Journal: Front Immunol Date: 2022-06-09 Impact factor: 8.786