Anthony Atala
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Anthony Atala, M.D., is the Director of the Wake Forest Institute for Regenerative Medicine, and Chair of the Department of Urology at the Wake Forest University School of Medicine in the state of North Carolina in the United States.[1] Regenerative medicine is "a practice that aims to refurbish diseased or damaged tissue using the body's own healthy cells."[2]
Atala was born in Peru in 1958,[3] grew up in Boca Raton, Florida, and comes from a large family.[4]. Atala attended the University of Miami and has an undergraduate degree in Psychology.[5] He went to medical school at the University of Louisville where he also completed his residency in urology. He was a fellow at the Harvard Medical School affiliated Boston Children's Hospital from 1990-1992 where he trained under world renowned pediatric urologic surgeons Alan Retik and Hardy Hendren. He served as the Director of the Laboratory for Tissue Engineering and Cellular Therapeutics at the Harvard Children's Hospital.[6] His work there involved growing human tissues and organs to replace those damaged by disease or defects. This work became important due to shortages in the organ-donor program.[7]
Dr. Atala continued his work in Tissue engineering and Printable organs[8] at Wake Forest University in 2004.[9] Dr. Atala led the team that developed the first lab-grown organ, a bladder, to be implanted into a human.[10] [11]
Aside from his ground breaking research, Dr. Atala is also tends to clinical and administrative responsibilities. He operates regularly and runs a busy clinic at the North Carolina Baptist Hospital, the teaching hospital of the Wake Forest University School of Medicine. He is also in charge of a rapidly growing urology department and has been successful in recruiting other renowned faculty to Wake Forest such as Gopal Badlani, James Yoo and Gordon McLorie.
Along with Harvard University researchers and as described in the journal Nature Biotechnology[12], he has announced that stem cells with enormous potential can be harvested from the amniotic fluid of pregnant women. These stems cells are pluripotent, meaning they can be manipulated to differentiate into various types of mature cells that make up nerve, muscle, bone, and other tissues while avoiding the problems of tumor formation and ethical concerns that are associated with embryonic stem cells.[13]
With respect to the amniotic fluid stem cells ("AFS" cells)[14], Dr. Atala said the following:
"The cells come from the foetus, which breathes and sucks in, then excretes, the amniotic fluid throughout pregnancy;"
"Like embryonic stem cells, they appear to thrive in lab dishes for years, while normal cells, called somatic cells, die after a time ;"
"They are easier to grow than human embryonic stem cells. And, unlike embryonic stem cells, they do not form a type of benign tumour called a teratoma;" and
"A bank with 100,000 specimens of the amniotic stem cells theoretically could supply 99 per cent of the US population with perfect genetic matches for transplants."[15]
Dr. Atala's work was seized on by opponents of the Embryonic Stem Cell Research Bill[16] (a part of the 100-Hour Plan of the Democratic Party in the 110th United States Congress) as a more moral alternative. He wrote a letter saying, inter alia, "Some may be interpreting my research as a substitute for the need to pursue other forms of regenerative medicine therapies, such as those involving embryonic stem cells. I disagree with that assertion." [17]
External links
Peer-reviewed journals
Stem cells |
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Sources: Embryonic stem cells | Adult stem cells | Cancer stem cells Related articles: Stem cell treatments | Stem cell controversy | Stem cell line | Progenitor cell | Cellular differentiation |
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
