Oct4-Induced Pluripotency in Adult Neural Stem Cells

نویسندگان

  • Jeong Beom Kim
  • Vittorio Sebastiano
  • Guangming Wu
  • Marcos J. Araúzo-Bravo
  • Philipp Sasse
  • Luca Gentile
  • Kinarm Ko
  • David Ruau
  • Mathias Ehrich
  • Dirk van den Boom
  • Johann Meyer
  • Karin Hübner
  • Christof Bernemann
  • Claudia Ortmeier
  • Martin Zenke
  • Bernd K. Fleischmann
  • Holm Zaehres
  • Hans R. Schöler
چکیده

The four transcription factors Oct4, Sox2, Klf4, and c-Myc can induce pluripotency in mouse and human fibroblasts. We previously described direct reprogramming of adult mouse neural stem cells (NSCs) by Oct4 and either Klf4 or c-Myc. NSCs endogenously express Sox2, c-Myc, and Klf4 as well as several intermediate reprogramming markers. Here we report that exogenous expression of the germline-specific transcription factor Oct4 is sufficient to generate pluripotent stem cells from adult mouse NSCs. These one-factor induced pluripotent stem cells (1F iPS) are similar to embryonic stem cells in vitro and in vivo. Not only can these cells can be efficiently differentiated into NSCs, cardiomyocytes, and germ cells in vitro, but they are also capable of teratoma formation and germline transmission in vivo. Our results demonstrate that Oct4 is required and sufficient to directly reprogram NSCs to pluripotency.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

G9a and Jhdm2a regulate embryonic stem cell fusion-induced reprogramming of adult neural stem cells.

Somatic nuclei can be reprogrammed to pluripotency through fusion with embryonic stem cells (ESCs). The underlying mechanism is largely unknown, primarily because of a lack of effective approaches to monitor and quantitatively analyze transient, early reprogramming events. The transcription factor Oct4 is expressed specifically in pluripotent stem cells, and its reactivation from somatic cell g...

متن کامل

P-92: Assessment of Stem Cells in Adult Mouse Ovaries during Estrous Cycle

Background: The concepts of reproductive biology were changed by stating the ovarian reserve in postnatal mammalian females is replenished. The aim of this study was to investigate the expression of OCT4 in the mice ovarian tissue during different stages of mouse estrous cycle. Materials and Methods: The mice were considered as pro-estrous, estrous, met-estrous and di-estrous based on the cell ...

متن کامل

Neural Stem Cells Achieve and Maintain Pluripotency without Feeder Cells

BACKGROUND Differentiated cells can be reprogrammed into pluripotency by transduction of four defined transcription factors. Induced pluripotent stem cells (iPS cells) are expected to be useful for regenerative medicine as well as basic research. Recently, the report showed that mouse embryonic fibroblasts (MEF) cells are not essential for reprogramming. However, in using fibroblasts as donor c...

متن کامل

P-99: Evaluation of Pluripotency Markers of Mouse Endometrial Tissue in Different Stages of Estrous Cycle

Background: It is assumed that adult stem/progenitor cells are responsible for cycling remodeling of the uterus endometrium throughout the reproductive life of the female. This study aimed to identify and localize stem/progenitor cells in the mice uterus using immunohistochemistry. Materials and Methods: 6-8 weeks old virgin female NMRI mice were submitted to the vaginal smear examination to de...

متن کامل

Functional roles of pluripotency transcription factors in mesenchymal stem cells

Pluripotency, the capacity of a cell to give rise to differentiated derivatives that represent each of the three primary germ layers, belongs to the cells that are located within the inner cell mass (ICM) of the developing blastocyst. Functional studies have identified a group of transcription factors, the pluripotency transcription factors that affect the pluripotent capacity. Within this grou...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Cell

دوره 136  شماره 

صفحات  -

تاریخ انتشار 2009