scholarly journals From mammalian tissue engineering to 3D plant cell culture

2016 ◽  
Vol 38 (4) ◽  
pp. 32-35 ◽  
Author(s):  
Raymond Wightman ◽  
C.J. Luo

Recent advances applying mammalian tissue engineering to in vitro plant cell culture have successfully cultured single plant cells in a 3D microstructure, leading to the discovery of plant cell behaviours that were previously not envisaged. Animal and plant cells share a number of properties that rely on a hierarchical microenvironment for creating complex tissues. Both mammalian tissue engineering and 3D plant culture employ tailored scaffolds that alter a cell's behaviour from the initial culture used for seeding. For humans, these techniques are revolutionizing healthcare strategies, particularly in regenerative medicine and cancer studies. For plants, we predict applications both in fundamental research to study morphogenesis and for synthetic biology in the agri-biotech sector.

2020 ◽  
Author(s):  
Alexander Mehring ◽  
Judith Stiefelmaier ◽  
Roland Ulber

<p>Biofilms are typically characterized as a consortium of microorganisms, which adhere to each other and often to surfaces. This adhesion is realized by extracellular polymeric substances (EPS), which are secreted by the microorganisms and mainly consist of water, polysaccharides, proteins and lipids as well as nucleic acids and lysis products [1]. Although cultured plant cells are not typically considered biofilms, parallels can be found in the properties of plant calli. These callus cells tend to form cohesive aggregates, owing to their extracellular matrix, and often strongly adhere to the agar plates they are kept on. The extracellular matrix of plant cells is mainly composed of structural polysaccharides, such as xyloglucans, arabinogalactans [2], homogalacturonan and extensins [3] among others. Cultured plant cells were found to adhere to surfaces before [4]. Surface-associated plant cell culture may have potential in a (semi‑)continuous cultivation including product secretion, as was shown in principle for alginate-embedded plant cells [5]. For cyanobacterial biofilms, an efficient strategy for EPS extraction was recently developed [6]. The transferability of these protocols to biofilm-like growing plant calli of Ocimum basilicum is currently being investigated. Subsequently, the composition of the extracellular matrix extracted from cultured O. basilicum cells is of interest. Furthermore, the adhesive properties of O. basilicum suspension cultures to microstructured surfaces and the potential role of the extracellular matrix are under investigation. An investigation of culture properties in an aerosol photobioreactor [7] is planned as well.</p> <p>This project is financially supported by the German research foundation (DFG, project number SFB 926-C03).</p> <p> </p> <p>References:</p> <p>[1]      H. C. Flemming, T. R. Neu, and D. J. Wozniak, “The EPS matrix: The ‘House of Biofilm Cells,’” J. Bacteriol., vol. 189, no. 22, pp. 7945–7947, 2007.</p> <p>[2]      I. M. Sims, K. Middleton, A. G. Lane, A. J. Cairns, and A. Bacic, “Characterisation of extracellular polysaccharides from suspension cultures of members of the Poaceae,” Planta, vol. 210, no. 2, pp. 261–268, Jan. 2000.</p> <p>[3]      M. Popielarska-Konieczna, K. Sala, M. Abdullah, M. Tuleja, and E. Kurczyńska, “Extracellular matrix and wall composition are diverse in the organogenic and non-organogenic calli of Actinidia arguta,” Plant Cell Rep., no. 0123456789, 2020.</p> <p>[4]      R. J. Robins, D. O. Hall, D. ‐J Shi, R. J. Turner, and M. J. C. Rhodes, “Mucilage acts to adhere cyanobacteria and cultured plant cells to biological and inert surfaces,” FEMS Microbiol. Lett., vol. 34, no. 2, pp. 155–160, 1986.</p> <p>[5]      Y. Kobayashi, H. Fukui, and M. Tabata, “Berberine production by batch and semi-continuous cultures of immobilized Thalictrum cells in an improved bioreactor,” Plant Cell Rep., vol. 7, no. 4, pp. 249–252, 1988.</p> <p>[6]      D. Strieth, J. Stiefelmaier, B. Wrabl et al., “A new strategy for a combined isolation of EPS and pigments from cyanobacteria,” J. Appl. Phycol., no. Fromme 2008, Feb. 2020.</p> <p>[7]        S. Kuhne, D. Strieth, M. Lakatos, K. Muffler, and R. Ulber, “A new photobioreactor concept enabling the production of desiccation induced biotechnological products using terrestrial cyanobacteria,” J. Biotechnol., vol. 192, no. Part A, pp. 28–33, 2014.</p>


2018 ◽  
Vol 138 (5) ◽  
pp. S182
Author(s):  
C. Libon ◽  
N. Steward ◽  
A. Cousy ◽  
J. Rouquet ◽  
C. Issac-Visentin ◽  
...  

Weed Science ◽  
1991 ◽  
Vol 39 (3) ◽  
pp. 497-504 ◽  
Author(s):  
Reid J. Smeda ◽  
Stephen C. Weller

Tissue and cell culture offer weed scientists many opportunities to research herbicide effects on plants. This review will discuss examples in which plant cells grown in vitro have been used to study herbicide action. Plant cell and tissue culture have many advantages over the use of whole plants; however, several disadvantages that exist are discussed. Cell cultures can be established for most plant species and provide a relatively homogeneous system for studying herbicide action. Responses of plant cells to herbicides are usually correlated with responses at the whole plant level, and cells have the advantage of posing fewer physical barriers to herbicide uptake and translocation. Cell culture techniques discussed include: screening candidate herbicide compounds; investigating herbicide efficacy, mechanism of action, metabolism, and uptake; and ascertaining mechanisms of herbicide resistance, selecting for resistance, and regenerating crops.


2018 ◽  
Vol 102 (20) ◽  
pp. 8661-8675 ◽  
Author(s):  
Regine Eibl ◽  
Philipp Meier ◽  
Irène Stutz ◽  
David Schildberger ◽  
Tilo Hühn ◽  
...  

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