Epidermal Stem Cells Can Reverse Their Fate
表皮干细胞可以逆转它们的命运
基本信息
- 批准号:6441074
- 负责人:
- 金额:$ 7.35万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-09-28 至 2003-07-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): Homeostasis of continuously renewing adult
tissues, such as the epidermis and the hematopoietic system, is maintained by
somatic stem cells. These are undifferentiated, s elf-renewing cells, which
also produce daughter transient amplifying (TA) cells. TA cells undergo a
finite number of cell divisions before differentiating and leaving the
proliferative compartment, whereas the stem cells persist throughout the
lifetime of the organism [1]. We first directly demonstrated heterogeneity in
the proliferative cells of the epidermis in 1981 when we identified a small
cells [2]. Recently, we developed a sorting method that yields a viable
population of somatic stem cells from mouse epidermis [3]. We showed that these
stem cells have the capacity to regenerate the epidermis and to permanently
express a recombinant gene in the regenerated tissue. A few years ago it was
demonstrated that somatic stem cells have the remarkable capacity to
differentiate into other tissue types [4], and have a plasticity only expected
of embryonic stem cells. Our preliminary data suggest that this may also be
true for epidermal stem cells, and that they have the ability to differentiate
into both ectodermally- and mesenchymally-derived tissues, suggesting that
somatic epidermal stem cells can cross the ectoderm-mesoderm developmental
barrier. Therefore, our hypotheses are 1) that somatic epidermal stem cells can
function in a similar manner to embryonic stem cells during development, and 2)
that environmental (extrinsic) factors influence the developmental pathway for
somatic stem cells. To test these hypotheses, we propose 1) To determine
whether epidermal stem cells injected into blastocysts alter their phenotype
during development, and 2) to determine whether the injected epidermal stem
cells permanently function as part of the tissue or organ in which they reside.
描述(申请人提供):持续更新的成人的动态平衡
组织,如表皮和造血系统,是由
体细胞干细胞。这些是未分化的S精灵更新细胞,它
也产生子代瞬时放大(TA)细胞。TA细胞经历一种
在分化和离开细胞之前的有限数量的细胞分裂
增殖室,而干细胞持续存在于整个
生物体的寿命[1]。我们首先直接展示了异质性
1981年,我们发现了一种小的表皮增殖细胞
Cells[2]。最近,我们开发了一种排序方法,它可以产生一个可行的
小鼠表皮中的体细胞群体[3]。我们展示了这些
干细胞具有再生表皮和永久修复的能力。
在再生组织中表达重组基因。几年前是这样的
证明了体细胞干细胞具有显著的能力
分化为其他组织类型[4],并具有预期的可塑性
胚胎干细胞。我们的初步数据表明,这也可能是
对于表皮干细胞来说是正确的,它们具有分化的能力
外胚层和间质来源的组织,这表明
体细胞表皮干细胞可以穿越外胚层-中胚层发育
障碍。因此,我们的假设是:1)体表干细胞可以
在发育过程中以类似于胚胎干细胞的方式发挥作用,以及2)
环境(外在)因素影响儿童的发育途径
体细胞干细胞。为了检验这些假设,我们建议1)确定
胚泡内注射表皮干细胞是否会改变其表型
在发育期间,以及2)确定注射的表皮干细胞
细胞永久地作为它们所在的组织或器官的一部分发挥作用。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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JACKIE R BICKENBACH其他文献
JACKIE R BICKENBACH的其他文献
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{{ truncateString('JACKIE R BICKENBACH', 18)}}的其他基金
Role of OCT4 in reprogramming human skin keratinocytes
OCT4在人皮肤角质形成细胞重编程中的作用
- 批准号:
8197353 - 财政年份:2009
- 资助金额:
$ 7.35万 - 项目类别:
Role of OCT4 in reprogramming human skin keratinocytes
OCT4在人皮肤角质形成细胞重编程中的作用
- 批准号:
7996059 - 财政年份:2009
- 资助金额:
$ 7.35万 - 项目类别:
Role of OCT4 in reprogramming human skin keratinocytes
OCT4在人皮肤角质形成细胞重编程中的作用
- 批准号:
7577192 - 财政年份:2009
- 资助金额:
$ 7.35万 - 项目类别:
Role of OCT4 in reprogramming human skin keratinocytes
OCT4在人皮肤角质形成细胞重编程中的作用
- 批准号:
7754673 - 财政年份:2009
- 资助金额:
$ 7.35万 - 项目类别:
Age-related Responses of Epidermal Stem Cells to Environ
表皮干细胞对环境的年龄相关反应
- 批准号:
6496987 - 财政年份:2002
- 资助金额:
$ 7.35万 - 项目类别:
Age-related Responses of Epidermal Stem Cells to Environ
表皮干细胞对环境的年龄相关反应
- 批准号:
7035837 - 财政年份:2002
- 资助金额:
$ 7.35万 - 项目类别:
Age-related Responses of Epidermal Stem Cells to Environ
表皮干细胞对环境的年龄相关反应
- 批准号:
6627846 - 财政年份:2002
- 资助金额:
$ 7.35万 - 项目类别: