scholarly journals Adipose-derived human stem/stromal cells: comparative organ specific mitochondrial bioenergy profiles

SpringerPlus ◽  
2016 ◽  
Vol 5 (1) ◽  
Author(s):  
Alice S. Ferng ◽  
Katherine M. Marsh ◽  
Jamie M. Fleming ◽  
Renee F. Conway ◽  
David Schipper ◽  
...  
Keyword(s):  
Author(s):  
Sara Rolandsson Enes ◽  
Emma Åhrman ◽  
Anitha Palani ◽  
Oskar Hallgren ◽  
Leif Bjermer ◽  
...  

2001 ◽  
Author(s):  
Rene C. Krieg ◽  
Joachim Rauch ◽  
Juergen Seidl ◽  
Herbert G. Stepp ◽  
Helmut Messmann ◽  
...  

BMC Cancer ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Laura E Pascal ◽  
Young Ah Goo ◽  
Ricardo ZN Vêncio ◽  
Laura S Page ◽  
Amber A Chambers ◽  
...  

2019 ◽  
Vol 2 (3) ◽  
pp. e201900304 ◽  
Author(s):  
Ulrich Blache ◽  
Edward R Horton ◽  
Tian Xia ◽  
Erwin M Schoof ◽  
Lene H Blicher ◽  
...  

Mesenchymal stromal cells (MSCs) are key contributors of the tumour microenvironment and are known to promote cancer progression through reciprocal communication with cancer cells, but how they become activated is not fully understood. Here, we investigate how breast cancer cells from different stages of the metastatic cascade convert MSCs into tumour-associated MSCs (TA-MSCs) using unbiased, global approaches. Using mass spectrometry, we compared the secretomes of MCF-7 cells, invasive MDA-MB-231 cells, and sublines isolated from bone, lung, and brain metastases and identified ECM and exosome components associated with invasion and organ-specific metastasis. Next, we used synthetic hydrogels to investigate how these different secretomes activate MSCs in bioengineered 3D microenvironments. Using kinase activity profiling and RNA sequencing, we found that only MDA-MB-231 breast cancer secretomes convert MSCs into TA-MSCs, resulting in an immunomodulatory phenotype that was particularly prominent in response to bone-tropic cancer cells. We have investigated paracrine signalling from breast cancer cells to TA-MSCs in 3D, which may highlight new potential targets for anticancer therapy approaches aimed at targeting tumour stroma.


2011 ◽  
Vol 2 (6) ◽  
pp. 481-489 ◽  
Author(s):  
Maria-Simonetta Faussone Pellegrini ◽  
Laurenţiu M. Popescu

AbstractHere, we review the history, morphology, immunohistochemical phenotype, and presumptive roles of a new type of interstitial tissue cells, formerly called interstitial Cajal-like cells (ICLC) and by 2010 named ‘telocytes’ (TC). Many different techniques have been used to characterize TC and provide their unequivocal identification: (i) in vitro, cultures and isolated cells; (ii) in situ, fixed specimens examined by light and fluorescence microscopy, transmission (TEM) and scanning electron microscopy, and electron tomography. TEM allowed sure identification and characterization of the most peculiar feature of TC: the long, thin, and convoluted prolongations named ‘telopodes’. An enormous variety of antibodies have been tested, but presently none are reliable to specifically label TC. TC have a mesenchymal origin and are resident connective tissue (stromal) cells. Possible identification with ‘already identified’ stromal cell types (fibroblasts, fibrocytes, fibroblast-like cells, and mesenchymal stromal cells) is discussed. We conclude that in adulthood, most of the TC have the morphology of fibrocytes. Apparently, immunocytochemistry suggests that a variety of TC populations showing different, likely organ-specific, immunophenotypes might exist. Several roles have been hypothesized for TC: mechanical roles, intercellular signaling, guiding and nursing of immature cells during organogenesis, and being themselves a pool of precursors for many of the mesenchyme-derived cells in adulthood; however, none of these roles have been proven yet. On the basis of the available data, we propose TC may be key players in organ regeneration and repair.


2015 ◽  
Vol 168 (2) ◽  
pp. 159-169 ◽  
Author(s):  
Anne S. Cornelissen ◽  
Marijke W. Maijenburg ◽  
Martijn A. Nolte ◽  
Carlijn Voermans

2009 ◽  
Vol 181 (4S) ◽  
pp. 477-477
Author(s):  
Alvin Y Liu ◽  
Laura E Pascal ◽  
Young Ah Goo ◽  
Ricardo Z Vencio ◽  
Laura S Page

2015 ◽  
Vol 9 (9-10) ◽  
pp. 599 ◽  
Author(s):  
Hazem Orabi ◽  
Alexandre Rousseau ◽  
Véronique Laterreur ◽  
Stéphane Bolduc

Introduction: Due to the complications associated with the use of non-native biomaterials and the lack of local tissues, bioengineered tissues are required for surgical reconstruction of complex urinary tract diseases, including those of the urinary bladder. The selfassembly method of matrix formation using autologous stromal cells obviates the need for exogenous biomaterials. We aimed at creating novel ex-vivo multilayer urinary tissue from a single bladder biopsy.Methods: After isolating urothelial, bladder stromal and smooth muscle cells from bladder biopsies, we produced 2 models of urinary equivalents: (1) the original one with dermal fibroblasts and (2) the new one with bladder stromal cells. Dermal fibroblasts and bladder stromal cells were stimulated to form an extracellular matrix, followed by sequential seeding of smooth muscle cells and urothelial cells. Stratification and cellular differentiation were assessed by histology, immunostaining and electron microscopy. Barrier function was checked with the permeability test. Biomechanical properties were assessed with uniaxinal tensile strength, elastic modulus, and failure strain.Results: Both urinary equivalents could be handled easily and did not contract. Stratified epithelium, intact basement membrane, fused matrix, and prominent muscle layer were detected in both urinary equivalents. Bladder stromal cell-based constructs had terminally differentiated urothelium and more elasticity than dermal fibroblasts-based equivalents. Permeation studies showed that both equivalents were comparable to native tissues.Conclusions: Organ-specific stromal cells produced urinary tissues with more terminally differentiated urothelium and better biomechanical characteristics than non-specific stromal cells. Smooth muscle cells could be incorporated into the selfassembled tissues effectively. This multi-layer tissue can be used as a urethral graft or as a bladder model for disease modelling and pharmacotherapeutic testing.


2005 ◽  
Vol 173 (4S) ◽  
pp. 387-387
Author(s):  
Quan Wu ◽  
Jian-Dang Shi ◽  
Yu Liu ◽  
Ke-Ming Wang ◽  
Helmut Klocker ◽  
...  

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