Scientific News Health care Rheumatic illnesses UCSD BIOENGINEERS FABRICATE JOINT CARTILAGE WHICH MIMICS STRUCTURE AND FUNCTION OF NATURAL TISSUE
UCSD BIOENGINEERS
FABRICATE JOINT CARTILAGE WHICH MIMICS STRUCTURE AND FUNCTION OF NATURAL TISSUE
University of
California, San Diego (UCSD) bioengineers
have fabricated cartilage tissue which for the first time mimics the
multi-layered structure and cellular functions of natural articular cartilage.
The tissue is made entirely from biological
materials using a modification of a technique invented at Rush-Presbyterian-St.
Luke’s Medical Center, Chicago. The researchers hope this tissue could be
developed as an implant treatment for the millions of people who suffer from
cartilage damage associated with joint injuries, congenital defects, arthritis
and age-related degeneration.
Robert Sah, professor of bioengineering at the
UCSD Jacobs School of Engineering, led the study, conducted by graduate students
Travis Klein and Kelvin Li and staff researcher Barb Schumacher at UCSD, in
collaboration with Professors Koichi Masuda and Eugene Thonar of Rush. Klein
will describe the results at the Biomedical Engineering Society annual meeting
at 2:15 p.m. on Saturday, October 6 at the Sheraton Imperial in Durham, North
Carolina.
“We’ve designed a tissue made up of different
types of juvenile cartilage cells with the notion that the tissue could be
implanted into a patient and grow up to conform to the specific geometry of the
individual’s joint,” said Sah. Next steps in the research will be to conduct
animal trials to determine the efficacy of such an implant treatment.
Cartilage is the body’s shock absorber, a
cushion of durable tissue that protects the knee from a lifetime of walking,
bending and running. Though just a few millimeters thick, cartilage is
nevertheless quite complex, consisting of a surface, middle and deep region,
each with its own distinct composition and structure.
In previous research, Sah detailed the mechanical
properties of cartilage and found that it is soft at the surface, but 25 times
stiffer in the deep regions. Meanwhile, Barbara Schumacher, then at Rush, found
that the cells in the surface region make a key protein, called Superficial Zone
Protein, which is a major lubricant of joints.
Using this data, bioengineers at UCSD developed a
map for how to organize different types of chondrocytes to mimic the stratified
nature of cartilage tissue. They then grew this cell mix together using the ARC
(Alginate Recovered Chondrocyte) method developed at Rush, which suspends cells
in a gel until the cells begin to form their own matrix or scaffolding. The gel
is then removed, leaving an entirely biological tissue.
In laboratory tests, the researchers found that
the cells at the surface of their engineered tissue effectively secreted the key
molecule, Superficial Zone Protein, needed to lubricate the joint. In addition,
the cells at the surface were making tissue that was softer and had a less dense
matrix, while the cells in the deeper regions were spaced further apart and had
a more densely packed matrix, which made the tissue stiffer.
The researchers believe that the engineered
tissue will mature like cartilage does naturally in humans. During fetal
development, cartilage cells are densely packed, and the matrix is loosely knit.
But as a child grows and the matrix supporting the cartilage gets stronger,
cartilage cells spread out. By the time an individual reaches adulthood, the
cartilage is mature, the cells become less active, and the tissue is about four
fold stiffer than during early development.
The engineered tissue is like immature cartilage,
and the researchers believe this will give the implant an advantage because as
it continues to mature, it is likely to integrate well and conform to fit with
the patient’s surrounding cartilage and joint tissue.
###
Contact: Denine Hagen; dhagen@ucsd.edu;
858-534-2920; University of California - San
Diego
Source of the given news and the copyrights
belong to a University
of California - San Diego
Publishing date: October 18, 2001
Back
|