Brawley Crista, Matunis Erika
Department of Cell Biology, 725 North Wolfe Street, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Science. 2004 May 28;304(5675):1331-4. doi: 10.1126/science.1097676. Epub 2004 May 13.
Although the ability of engrafted stem cells to regenerate tissue has received much attention, the molecular mechanisms controlling regeneration are poorly understood. In the Drosophila male germline, local activation of the Janus kinase-signal transducer and activator of transcription (Jak-STAT) pathway maintains stem cells; germline stem cells lacking Jak-STAT signaling differentiate into spermatogonia without self-renewal. By conditionally manipulating Jak-STAT signaling, we find that spermatogonia that have initiated differentiation and are undergoing limited mitotic (transit-amplifying) divisions can repopulate the niche and revert to stem cell identity. Thus, in the appropriate microenvironment, transit-amplifying cells dedifferentiate, becoming functional stem cells during tissue regeneration.
尽管移植的干细胞再生组织的能力备受关注,但控制再生的分子机制却知之甚少。在果蝇雄性生殖系中,Janus激酶-信号转导子和转录激活子(Jak-STAT)通路的局部激活维持着干细胞;缺乏Jak-STAT信号的生殖系干细胞会分化为精原细胞,且不再自我更新。通过有条件地操纵Jak-STAT信号,我们发现已开始分化并正在进行有限有丝分裂(过渡增殖)的精原细胞能够重新占据微环境并恢复干细胞特性。因此,在合适的微环境中,过渡增殖细胞会去分化,在组织再生过程中成为功能性干细胞。