Transplanting Lacrimal Glands
Dry-Eye Disease involves the
dysfunction of this gland and is the most prevalent cause of corneal
damage. Lacrimal gland dysfunction can be caused by certain diseases,
environmental exposure, long-term visual work, contact lense use, as
side-effects from optical surgery, etc. Dry-Eye can result in
discomfort, loss of vision, and lost quality of life.
These researchers bioengineered their
mouse lacrimal gland using dissociated single cells from epithelial
and mesenchymal tissues of embryonic day-16.5 murine-lacrimal germ
and harderian gland germs. This method is called the organ germ
method, involving growing the cells in an organ culture. The gland
germs were engrafted in correct orientation on the eye of 7-week-old
mice with the utilization of an engineered epithelial,
tissue-connecting plastic device. Within 30 days, transplant growth
was apparent and overall, approximately 75% of the gland transplants
were successful, containing near-natural acini diameters and
characteristic pigments and also made successful connection to the
lacrimal duct, restoring secretory function.
This article is very interesting to me
because I have bad vision which continues to degrade and any
advancement of ophthalmic therapy could help me immensely someday.
Also, one of my family members has Dry-Eye Disease (DED) and I
experience first-hand how it can decrement daily experiences and
visual enjoyment. Current therapies such as artificial tears are not
completely satisfactory and also expensive. The development of
standard techniques for research and application of bioengineered
organs and transplants is very necessary for all of us to begin to
see fruits of its use, saving and improving lives, and in the
advancement of science in general.
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