* Department of Gynecology and Obstetrics, Johns Hopkins University
School of Medicine, Baltimore, MD 21287; Contributed by John W. Littlefield, November 9, 2000
Human pluripotent stem cells (hPSCs) have been derived from the
inner cell mass cells of blastocysts (embryonic stem cells) and
primordial germ cells of the developing gonadal ridge (embryonic germ
cells). Like their mouse counterparts, hPSCs can be maintained in
culture in an undifferentiated state and, upon differentiation, generate a wide variety of cell types. Embryoid body (EB) formation is
a requisite step in the process of in vitro
differentiation of these stem cells and has been used to derive neurons
and glia, vascular endothelium, hematopoietic cells, cardiomyocytes,
and glucose-responsive insulin-producing cells from mouse PSCs. EBs generated from human embryonic germ cell cultures have also been found
to contain a wide variety of cell types, including neural cells,
vascular endothelium, muscle cells, and endodermal derivatives. Here,
we report the isolation and culture of cells from human EBs as well as
a characterization of their gene expression during growth in several
different culture environments. These heterogeneous cell cultures are
capable of robust and long-term [>70 population doublings (PD)]
proliferation in culture, have normal karyotypes, and can be
cryopreserved, clonally isolated, and stably transfected. Cell cultures
and clonal lines retain a broad pattern of gene expression including
simultaneous expression of markers normally associated with cells of
neural, vascular/hematopoietic, muscle, and endoderm lineages. The
growth and expression characteristics of these EB-derived cells suggest
that they are relatively uncommitted precursor or progenitor cells.
EB-derived cells may be suited to studies of human cell differentiation
and may play a role in future transplantation therapies.
Cell Biology
Human embryonic germ cell derivatives express a broad range of
developmentally distinct markers and proliferate
extensively in vitro
,
,
,
,¶
Department of
Physiology, Johns Hopkins University School of Medicine, Baltimore, MD
21287;
Department of Gynecology and Obstetrics, Johns
Hopkins Bayview Hospital, Baltimore, MD 21214; and
§ Division of Immunology and Hematopoiesis, Johns Hopkins
University School of Medicine Oncology Center, Baltimore, MD 21231
¶
To whom reprint requests should be addressed. E-mail:
gearhart{at}jhmi.edu.
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