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Author Topic: Researchers Engineer Miniature Human Livers in the Lab  (Read 4092 times)
Zach
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"Still crazy after all these years."

« on: November 01, 2010, 08:12:36 AM »

http://www.wfubmc.edu/News-Releases/2010/Researchers_Engineer_Miniature_Human_Livers_in_the_Lab.htm#

11/1/10 11:04 AM

Researchers Engineer Miniature Human Livers in the Lab

Wake Forest University Baptist Medical Center
 
WINSTON-SALEM, N.C. – Saturday, Oct. 30, 2010 – Researchers at the Institute for Regenerative Medicine at Wake
Forest University Baptist Medical Center have reached an early, but important, milestone in the quest to grow
replacement livers in the lab. They are the first to use human liver cells to successfully engineer miniature livers
that function – at least in a laboratory setting – like human livers. The next step is to see if the livers will
continue to function after transplantation in an animal model.

The ultimate goal of the research, which will be presented Sunday at the annual meeting of the American
Association for the Study of Liver Diseases in Boston and published in an upcoming issue of the journal
Hepatology, is to provide a solution to the shortage of donor livers available for patients who need transplants.
Laboratory-engineered livers could also be used to test the safety of new drugs.

“We are excited about the possibilities this research represents, but must stress that we’re at an early stage and
many technical hurdles must be overcome before it could benefit patients,” said Shay Soker, Ph.D., professor of
regenerative medicine and project director. “Not only must we learn how to grow billions of liver cells at one time
in order to engineer livers large enough for patients, but we must determine whether these organs are safe to
use in patients.”

Pedro Baptista, PharmD, Ph.D., lead author on the study, said the project is the first time that human liver cells
have been used to engineer livers in the lab. “Our hope is that once these organs are transplanted, they will
maintain and gain function as they continue to develop,” he said.

The engineered livers, which are about an inch in diameter and weigh about .20 ounces, would have to weigh
about one pound to meet the minimum needs of the human body, said the scientists. Even at this larger size, the
organs wouldn’t be as large as human livers, but would likely provide enough function. Research has shown that
human livers functioning at 30 percent of capacity are able to sustain the human body.

To engineer the organs, the scientists used animal livers that were treated with a mild detergent to remove all
cells (a process called decellularization), leaving only the collagen “skeleton” or support structure. They then
replaced the original cells with two types of human cells: immature liver cells known as progenitors, and
endothelial cells that line blood vessels.

The cells were introduced into the liver skeleton through a large vessel that feeds a system of smaller vessels in
the liver. This network of vessels remains intact after the decellularization process. The liver was next placed in a
bioreactor, special equipment that provides a constant flow of nutrients and oxygen throughout the organ. 
After a week in the bioreactor system, the scientists documented the progressive formation of human liver tissue,
as well as liver-associated function. They observed widespread cell growth inside the bioengineered organ.
The ability to engineer a liver with animal cells had been demonstrated previously. However, the possibility of
generating a functional human liver was still in question.

The researchers said the current study suggests a new approach to whole-organ bioengineering that might prove
to be critical not only for treating liver disease, but for growing organs such as the kidney and pancreas.
Scientists at the Wake Forest Institute for Regenerative Medicine are working on these projects, as well as many
other tissues and organs, and also working to develop cell therapies to restore organ function.
Bioengineered livers could also be useful for evaluating the safety of new drugs. “This would more closely mimic
drug metabolism in the human liver, something that can be difficult to reproduce in animal models," said
Baptista.

Co-researchers were Dipen Vyas, B.Pharm., M.S., Zhan Wang, M.D., Ph.D. and Anthony Atala, M.D., director of the
institute.

© Wake Forest University Baptist Medical Center, Medical Center Boulevard, Winston-Salem, NC 27157. All Rights Reserved.
« Last Edit: November 01, 2010, 08:14:02 AM by Zach » Logged

Uninterrupted in-center (self-care) hemodialysis since 1982 -- 34 YEARS on March 3, 2016 !!
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
No transplant.  Not yet, anyway.  Only decided to be listed on 11/9/06. Inactive at the moment.  ;)
I make films.

Just the facts: 70.0 kgs. (about 154 lbs.)
Treatment: Tue-Thur-Sat   5.5 hours, 2x/wk, 6 hours, 1x/wk
Dialysate flow (Qd)=600;  Blood pump speed(Qb)=315
Fresenius Optiflux-180 filter--without reuse
Fresenius 2008T dialysis machine
My KDOQI Nutrition (+/ -):  2,450 Calories, 84 grams Protein/day.

"Living a life, not an apology."
Whamo
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« Reply #1 on: October 26, 2011, 10:17:46 AM »

I need a new kidney and a new liver, so I hope they hurry up, LOL.
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willowtreewren
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My two beautifull granddaughters

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« Reply #2 on: October 26, 2011, 11:13:23 AM »

This is encouraging news. My daughter will likely need a liver in the future.  :2thumbsup;

Thanks for sharing, Zach!
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
boswife
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us and fam easter 2013

« Reply #3 on: October 26, 2011, 07:31:19 PM »

WHERE ARE YOU ZACH??????
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im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
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