The annual
Orthopaedic Research Society meeting was an energetic and collaborative
conference attended by clinicians, industry professionals, and researchers. While
the attendees brought diverse perspectives to this meeting, the varied
presentation styles, such as short poster teasers, mid-length research talks,
and longer, broader spotlight oral presentations helped bring the audience
together in scientific discourse. With over 300 oral presentations and over 2200
poster presentations, the variety in presentation styles made ORS 2017 an
engaging and dynamic conference to attend.
Knockdown of vimentin may affect chondrogenic extracellular matrix deposition in high density pellets. shVim-vimentinknockdown, shLacZ-control. |
My
research in Dr. Adam H. Hsieh’s Orthopaedic Mechanobiology Lab at the University of Maryland centers on the role
of vimentin intermediate filaments in governing mesenchymal stem cell (MSC) properties and behavior, including cellular deformability, adhesion, and
differentiation, specifically chondrogenesis. After knocking down the
expression of vimentin intermediate filaments in human MSCs using RNA interference, we
observe how a decrease in vimentin affects differentiation (abstract here). Preliminarily,
we’ve found that a decrease in vimentin did not affect adipogenesis or
osteogenesis, but may lead to a potential decrease in chondrogenic extracellular
matrix deposition, but this needs further exploration. MSCs from RoosterBio
have been singular in the progression of my graduate research. The fast growth
and consistency of the high quality MSCs have taken the bottleneck of MSC
growth out of the equation for my research. Further, using these MSCs and media
has dramatically decreased the labor, time, and resources needed to obtain the
cell numbers needed for conducting my experiments.
During this
conference, I was able to have in-depth conversations about my research as well
as exchange ideas and technical tips that will help strengthen my work.
Attending ORS allowed me to both present my research through a poster
presentation and network with both industry professionals and academic researchers.
As I will soon be taking the next step in my career, these interactions helped
me to start to home in on the types of opportunities that I would like to
pursue and how to prepare myself to excel. Further, attending professional
development seminars, such as one regarding the art of negotiation, helped me
identify techniques for further developing soft skills.
One of the
most engaging sessions in this conference was a really fun debate about the
related futures of regenerative medicine and orthopaedic implants – Will Regenerative Medicine Make Orthopaedic Implants
Obsolete in Our Time? It was captivating to hear the discussion about two research
and clinical areas that continue to intersect and diverge. Also, the keynote by
Dr. Jennifer Doudna summarizing the CRISPR technology that she helped develop
was a great overview and the brief discussion about the ethics of gene therapy
was thought-provoking.
The
research presentations and broader spotlight sessions gave me a great overview
of the latest research in my interest areas of regenerative medicine, tissue
engineering, cell therapies, and biomaterials. Many of the oral presentations I
attended focused on bettering the design of tissue engineered scaffolds. Here
are just a few of the research presentations that inspired me:
Development of a Continuous
Dual-Gradient Peptide Scaffold for Directed Osteochondral Spatial
Differentiation
·
Dr.
Jennifer L. Puetzer, Stevens Lab, Imperial College London
·
Dr.
Puetzer presented a sequentially electrospun polycaprolactone scaffold with
opposing gradients of two peptides in a single scaffold for osteochondral
repair. MSCs seeded on the glycosaminoglycan-binding
peptide side of the scaffold showed chondrogenic differentiation while those
seeded on the mineral nucleating peptide side showed osteogenic differentiation
without any exogenous growth factors!
·
Learn
more about their dual gradient peptide research here.
A Bi-layered Scaffold Derived from
Decellularized Growth Plate and Articular Cartilage Extracellular Matrix for
Osteochondral Defect Repair
·
Dr.
Grainne Cunniffe, Kelly Lab, Trinity College Dublin
·
Dr.
Cunniffe presented a bi-layered scaffold for osteochondral repair using
decellularized and homogenized growth plate and articular cartilage
extracellular matrices. In vitro,
MSCs seeded onto the scaffold differentiated in response to the different
extracellular matrix cues, with more glycosaminoglycans found on the cartilage-derived
matrix and calcification found on the growth plate-derived matrix. In an in vivo goat osteochondral defect model,
hyaline cartilage and endochondral ossification were observed by 12 months.
·
Learn
more about their extracellular matrix-derived scaffolds here.
Mesenchymal Stem Cells Expressing the Cell Adhesion Molecule CD146 Present Increased Homing Towards Degenerative Intervertebral Discs - an Organ Culture Study
·
Sebastian
Wangler, Grad Lab, AO Research Institute
·
Sebastian
Wangler presented a series of studies to characterize MSC homing to
degenerative intervertebral discs. MSCs migrating toward both a degenerative
disc chemoattractant and conditioned media from an induced degenerative disc
model expressed higher levels of the marker CD146 compared to controls.
Further, in an induced degenerative disc organ study, CD146+ MSCs showed
increased migration into the discs compared to CD146- MSCs.
·
Learn
more about MSC homing to chemoattractant cues from degenerative discs here.
This
year’s ORS annual meeting was really engaging and was excellent for fostering
discussion about the latest research in orthopaedics, professional development,
and networking. I enjoyed presenting my research at ORS and am thankful to
RoosterBio for their high-quality MSCs, media systems, and service as well as
their support toward my attendance at ORS 2017!
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