Expansion of Adipose Derived Stromal Cells from Stromal Vascular Fraction in a Single-Use Bioreactor: Proof of Concept in the Mobius® 3L

Cytotherapy ◽  
2016 ◽  
Vol 18 (6) ◽  
pp. S138
Author(s):  
M. Gadelorge ◽  
M. Bourdens ◽  
C. Bardiaux ◽  
N. Espagnolle ◽  
J. Murrell ◽  
...  
2019 ◽  
Vol 35 (04) ◽  
pp. 358-367 ◽  
Author(s):  
Joris A. van Dongen ◽  
Joeri van Boxtel ◽  
Martin C. Harmsen ◽  
Hieronymus P. Stevens

AbstractLipofilling, the transplantation of adipose tissue, has already been used since the end of the 19th century. For decades, lipofilling was used to restore loss of volume due to aging, trauma, or congenital defects. Later on, the indications for the use of lipofilling expanded by treating aged skin, scars, and improving wound healing. The expansion was caused by the discovery of adipose derived stromal cells (ASCs) in adipose tissue and the development of very fine harvesting and injection cannulas which made it possible to inject small adipose tissue particles in small volume areas, such as the face. ASCs are multipotent stromal cells which reside in the stromal vascular fraction (SVF) of adipose tissue and are able to differentiate in multiple cell lineages and secrete a plurality of growth factors with regenerative potentials. The discovery of ASCs led toward more experimental cell-based therapies, that is, ASCs or SVF isolated by means of enzymatic isolation procedures. Later on, enzymatic isolation procedures were forbidden in many countries by legislation and were replaced by mechanical isolation procedures, such as the Nanofat and Fractionation of Adipose Tissue (FAT) procedures. The Nanofat procedure has been extensively investigated, especially as treatment for skin rejuvenation in the face. Though, substantial evidence is lacking for using facial lipofilling or any therapeutic component, that is, ASCs or SVF for skin rejuvenation to date. In contrast, facial lipofilling to restore loss of volume seems to be promising.


2017 ◽  
Vol 139 (4) ◽  
pp. 911-914 ◽  
Author(s):  
Elizabeth R. Zielins ◽  
Elizabeth A. Brett ◽  
Charles P. Blackshear ◽  
John Flacco ◽  
Ryan C. Ransom ◽  
...  

2021 ◽  
Vol 17 (7) ◽  
pp. e1009228
Author(s):  
Kaiyi Zhu ◽  
Lingyi Cai ◽  
Chenqian Cui ◽  
Juan R. de los Toyos ◽  
Dimitris Anastassiou

During the last ten years, many research results have been referring to a particular type of cancer-associated fibroblasts associated with poor prognosis, invasiveness, metastasis and resistance to therapy in multiple cancer types, characterized by a gene expression signature with prominent presence of genes COL11A1, THBS2 and INHBA. Identifying the underlying biological mechanisms responsible for their creation may facilitate the discovery of targets for potential pan-cancer therapeutics. Using a novel computational approach for single-cell gene expression data analysis identifying the dominant cell populations in a sequence of samples from patients at various stages, we conclude that these fibroblasts are produced by a pan-cancer cellular transition originating from a particular type of adipose-derived stromal cells naturally present in the stromal vascular fraction of normal adipose tissue, having a characteristic gene expression signature. Focusing on a rich pancreatic cancer dataset, we provide a detailed description of the continuous modification of the gene expression profiles of cells as they transition from APOD-expressing adipose-derived stromal cells to COL11A1-expressing cancer-associated fibroblasts, identifying the key genes that participate in this transition. These results also provide an explanation to the well-known fact that the adipose microenvironment contributes to cancer progression.


2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Himanshu Bansal ◽  
Kristin Comella ◽  
Jerry Leon ◽  
Poonam Verma ◽  
Diwaker Agrawal ◽  
...  

This article has been retracted. Please see the Retraction Notice for more detail: https://doi.org/10.1186/s12967-021-02852-z


2020 ◽  
Author(s):  
Kaiyi Zhu ◽  
Lingyi Cai ◽  
Chenqian Cui ◽  
Dimitris Anastassiou

AbstractDuring the last ten years, many research results have been referring to a particular type of cancer-associated fibroblasts associated with invasiveness, metastasis and resistance to therapy, characterized by a gene expression signature, identical in multiple types of solid cancer, with prominent presence of collagen COL11A1. Identifying the underlying biological mechanisms responsible for their creation may help towards the identification of drug targets for pan-cancer therapeutics. We have performed an extensive computational analysis of single-cell gene expression data from many cancer types, concluding that these fibroblasts are produced by a transformation of adipose-derived stromal cells naturally occurring in the stromal vascular fraction of the adipose microenvironment. Focusing on a rich pancreatic cancer dataset, we provide a detailed description of the continuous modification of the gene expression profile of the cells as they transition from APOD-expressing adipose-derived stromal cells to COL11A1-expressing cancer-associated fibroblasts, identifying the key genes that participate in this transformation.Statement of significanceThis work provides an explanation to the well-known fact that the adipose microenvironment contributes to cancer progression. It also describes an underlying biological mechanism involving the transformation of adipose-derived stromal cells into COL11A1-expressing cancer-associated fibroblasts, at which point metastasis is imminent, with potential of pan-cancer therapeutics targeting those mechanisms.


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