Author
Listed:
- Silvia A. Ferreira
(King’s College London)
- Meghna S. Motwani
(King’s College London)
- Peter A. Faull
(The Francis Crick Institute)
- Alexis J. Seymour
(King’s College London)
- Tracy T. L. Yu
(King’s College London)
- Marjan Enayati
(King’s College London
Medical University of Vienna)
- Dheraj K. Taheem
(King’s College London)
- Christoph Salzlechner
(King’s College London)
- Tabasom Haghighi
(King’s College London)
- Ewa M. Kania
(King’s College London)
- Oommen P. Oommen
(Tampere University of Technology and BioMediTech Institute)
- Tarek Ahmed
(University College London)
- Sandra Loaiza
(Imperial College London)
- Katarzyna Parzych
(Imperial College London)
- Francesco Dazzi
(King’s College London)
- Oommen P. Varghese
(Uppsala University)
- Frederic Festy
(King’s College London)
- Agamemnon E. Grigoriadis
(King’s College London)
- Holger W. Auner
(Imperial College London)
- Ambrosius P. Snijders
(The Francis Crick Institute)
- Laurent Bozec
(University College London
124 Edward Street, Toronto)
- Eileen Gentleman
(King’s College London)
Abstract
Modifiable hydrogels have revealed tremendous insight into how physical characteristics of cells’ 3D environment drive stem cell lineage specification. However, in native tissues, cells do not passively receive signals from their niche. Instead they actively probe and modify their pericellular space to suit their needs, yet the dynamics of cells’ reciprocal interactions with their pericellular environment when encapsulated within hydrogels remains relatively unexplored. Here, we show that human bone marrow stromal cells (hMSC) encapsulated within hyaluronic acid-based hydrogels modify their surroundings by synthesizing, secreting and arranging proteins pericellularly or by degrading the hydrogel. hMSC’s interactions with this local environment have a role in regulating hMSC fate, with a secreted proteinaceous pericellular matrix associated with adipogenesis, and degradation with osteogenesis. Our observations suggest that hMSC participate in a bi-directional interplay between the properties of their 3D milieu and their own secreted pericellular matrix, and that this combination of interactions drives fate.
Suggested Citation
Silvia A. Ferreira & Meghna S. Motwani & Peter A. Faull & Alexis J. Seymour & Tracy T. L. Yu & Marjan Enayati & Dheraj K. Taheem & Christoph Salzlechner & Tabasom Haghighi & Ewa M. Kania & Oommen P. O, 2018.
"Bi-directional cell-pericellular matrix interactions direct stem cell fate,"
Nature Communications, Nature, vol. 9(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-06183-4
DOI: 10.1038/s41467-018-06183-4
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