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Thyroid function may be restored through patient-derived human cells

Discovery could help lead to treatments for patients with thyroid cancer, children with congenital hypothyroidism

Date:
October 22, 2015
Source:
Beth Israel Deaconess Medical Center
Summary:
A discovery has been made that could one day restore thyroid function in patients with cancer whose thyroids have been surgically removed or in children born with congenital hypothyroidism.
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A discovery made by investigators from Beth Israel Deaconess Medical Center (BIDMC) and the Boston University School of Medicine (BUSM) may help lead to the development of a cell-based regenerative therapy to restore thyroid function in patients with cancer who have had their thyroids surgically removed and children born with congenital hypothyroidism. The new findings are described in the Oct. 22 issue of Cell Stem Cell.

"This research represents an important step toward the goal of being able to better treat thyroid diseases and being able to permanently rescue thyroid function through the transplantation of a patient's own engineered pluripotent stem cells," explained co-corresponding author Anthony N. Hollenberg, MD, Chief of the Division of Endocrinology, Diabetes and Metabolism at BIDMC and Professor of Medicine at Harvard Medical School.

"Until now, we haven't fully understood the natural process that underlies early thyroid development," said co-corresponding author Darrell N. Kotton, MD, Director of the Center for Regenerative Medicine (CReM) at BUSM and Boston Medical Center and Professor of Medicine and Pathology at BUSM. "With this paper, we've identified the signaling pathways in thyroid cells that regulate their differentiation, the process by which unspecialized stem cells give rise to specialized cells during early fetal development."

After deciphering this natural differentiation process, the investigators duplicated it in the laboratory dish by adding a sequence of proteins, called growth factors, to the fluid bathing the stem cells. The team then used murine pluripotent stem cells to regenerate thyroid function in a murine model of hypothyroidism. Next, they adapted this method using induced pluripotent stem cells (iPSCs) engineered from children with congenital hypothyroidism, who are born with genetic defects that prevent their thyroids from fully developing.

Hypothyroidism results when the thyroid gland produces too little thyroid hormone, which impairs metabolism and can result in slowed heart rate, weight gain and chronic symptoms of feeling cold and tired with decreased mental acuity. Although drugs are available to replace thyroid function, with this new discovery, "we can now envision that thyroid function could be restored by transplanting patients' own thyroid cells," said Hollenberg and Kotton.


Story Source:

Materials provided by Beth Israel Deaconess Medical Center. Note: Content may be edited for style and length.


Journal Reference:

  1. Anita A. Kurmann et al. Regeneration of Thyroid Function by Transplantation of Differentiated Pluripotent Stem Cells. Cell Stem Cell, October 2015 DOI: 10.1016/j.stem.2015.09.004

Cite This Page:

Beth Israel Deaconess Medical Center. "Thyroid function may be restored through patient-derived human cells: Discovery could help lead to treatments for patients with thyroid cancer, children with congenital hypothyroidism." ScienceDaily. ScienceDaily, 22 October 2015. <www.sciencedaily.com/releases/2015/10/151022124516.htm>.
Beth Israel Deaconess Medical Center. (2015, October 22). Thyroid function may be restored through patient-derived human cells: Discovery could help lead to treatments for patients with thyroid cancer, children with congenital hypothyroidism. ScienceDaily. Retrieved May 29, 2017 from www.sciencedaily.com/releases/2015/10/151022124516.htm
Beth Israel Deaconess Medical Center. "Thyroid function may be restored through patient-derived human cells: Discovery could help lead to treatments for patients with thyroid cancer, children with congenital hypothyroidism." ScienceDaily. www.sciencedaily.com/releases/2015/10/151022124516.htm (accessed May 29, 2017).

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