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“男性移植自体的干细胞”可能有助于治疗1型糖尿病 [复制链接]

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发表于 2010-12-13 10:39 |只看该作者 |倒序浏览 |打印
本帖最后由 qingshui1985 于 2010-12-13 10:41 编辑
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主题:“男性移植自体的干细胞”可能有助于治疗1型糖尿病; @* u7 l5 p5 W

- W) Y; _/ o  O9 S说明:原文来源http://www.sciencedaily.com/releases/2010/12/101212121739.htm8 m3 s! h/ _4 c- }" o0 l
由干细胞之家新闻小组成员qingshui1985翻译(转帖请注明)
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乔治敦大学医学中心研究人员发现,男性1型糖尿病或许可以从他们的睾丸组织产生胰岛细胞。这一成果在美国费城12月12日的第50届细胞生物学学会年会上公布。
5 e# F8 d. K2 x(注:1型糖尿病(Ⅰ型糖尿病),是由于免疫系统发育不良或免疫应激引发的糖尿病。又名胰岛素依赖型糖尿病(IDDM)或青少年糖尿病,易出现糖尿病酮症酸中毒(DKA)。又叫青年发病型糖尿病,这是因为它常常在35岁以前发病,占糖尿病的10%以下。1型糖尿病是依赖胰岛素治疗的,也就是说病友从发病开始就需使用胰岛素治疗,并且终身使用。)8 J5 X. x: s$ B8 G* y2 O' _
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他们实验室研究证实男性的睾丸提取出来的精原干细胞可以变成beta胰岛细胞,并能正常的产生胰岛素。而且他们不使用额外的基因,即完成了成人的干细胞分化成胰岛细胞这一壮举。/ {! U* p, n% G8 r3 r* y

" z+ _4 C; M6 L0 D3 z. a: c“现有的人类的干细胞、成体细胞或胚胎细胞都不能诱导产生治疗糖尿病足量的胰岛素。但是我们知道精原干细胞具有这一潜能,因而我们知道如何去完成这一研究。”说这项研究的主要研究者,乔治敦大学医学中心细胞生物学及转基因核心实验室主任 克伊恩Gallicano,博士说道。, c- D+ s0 @+ P) d6 d8 P

/ \9 T; q1 H$ H1 B鉴于不断取得的进展,Gallicano博士说,他们的策略可以提供治疗1型糖尿病(幼年发病)的独特的解决方法。已经有几个新的疗法尝试治疗糖尿病。但是都有缺点。研究人员曾利用小鼠的ips治疗糖尿病,但是这一方法容易产生畸胎瘤,或肿瘤。以及重编程会引入外源的基因,因而存在较大问题。, Q$ g  ?& m6 v( ~, t
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乔治敦大学研究人员以精子细胞的前体细胞精原干细胞取代ips细胞,进行了实验。实验材料来源于一些捐献的死者的人体器官。
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7 L7 @' K* t8 D( Y2 |, B; t( Z3 D由于精原干细胞具有形成胚胎干细胞的相关基因,所以不需要导入外源基因使得它们重编程。Gallicano博士说:“这些男性的生殖干细胞具有成体多能干细胞的能力”
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“我们发现一旦将这些细胞从睾丸分离,它们就会退分化,数周后具有形成3个胚层组织的能力”,他说,这些精原干细胞退分化后形成的是真正的多能干细胞。
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  F: x$ z1 `' \# e该研究小组在实验室下从睾丸提取了1g组织,产生了100万个干细胞。这些细胞显示了很多正常的胰岛细胞的标志物特征。% @, B+ b2 }, E+ y
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他们随后将这些细胞移植到类似于糖尿病免疫缺陷小鼠中。而这些细胞在一周后能够降低小鼠的血糖水平,证实这些细胞产生了足量的胰岛素降低血糖。9 ]$ w3 s& J+ T; L, Y/ L
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虽然要一周时间见效,但是Gallicano博士新的研究表明其治疗效果比以前的方法大幅度提高。8 ~. w- W1 D7 r4 s7 Y1 s

2 }9 i# {3 E% `; B- E% y) Z# m+ L# [这项研究由美国糖尿病协会等基金资助。/ d; [, u) u- t: Y' L7 j; |2 Z
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个人翻译,理解不准确的语句还望大家积极指出。7 f' D( b1 T1 N+ P
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沙发
发表于 2010-12-13 10:40 |只看该作者
本帖最后由 qingshui1985 于 2010-12-13 10:42 编辑 2 }. v* j' f9 |5 t$ g5 R0 m" p

/ w+ ^6 A; R3 o- J, Y5 J本文是会议论文,没有查到全文。
- B( H8 S+ R: Z% b( r仅有英语文稿:2 Q* `( H  A8 i+ I7 ?5 m, }: ]) `
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'Grow Your Own Transplant' May Be Possible for Men With Type 1 Diabetes
6 p) L: L+ A4 d! X3 I- WMen with type 1 diabetes may be able to grow their own insulin-producing cells from their testicular tissue, say Georgetown University Medical Center (GUMC) researchers who presented their findings December 12 at the American Society of Cell Biology 50th annual meeting in Philadelphia.
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( R5 H5 o& }  \2 h* pTheir laboratory and animal study is a proof of principle that human spermatogonial stem cells (SSCs) extracted from testicular tissue can morph into insulin-secreting beta islet cells normally found in the pancreas. And the researchers say they accomplished this feat without use of any of the extra genes now employed in most labs to turn adult stem cells into a tissue of choice., f) }) [3 r9 i8 z6 C. @' R$ B" H
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"No stem cells, adult or embryonic, have been induced to secrete enough insulin yet to cure diabetes in humans, but we know SSCs have the potential to do what we want them to do, and we know how to improve their yield," says the study's lead investigator, G. Ian Gallicano, Ph.D., an associate professor in the Department of Cell Biology and Director of the Transgenic Core Facility at GUMC.' z" O/ ~2 m" @/ \6 U
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Given continuing progress, Gallicano says his strategy could provide a unique solution to treatment of individuals with type 1 diabetes (juvenile onset diabetes). Several novel therapies have been tried for these patients, but each has drawbacks. Transplanting islet cells from deceased donors can result in rejection, plus few such donations are available. Researchers have also cured diabetes in mice using induced pluripotent stem (IPS) cells -- adult stem cells that have been reprogrammed with other genes to behave like embryonic stem cells -- but this technique can produce teratomas, or tumors, in transfected tissue, as well as problems stemming from the external genes used to create IPS cells, Gallicano says.
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3 H% Q9 i7 i: m# T) u2 |* dInstead of using IPS cells, the researchers turned to a readily available source of stem cells, the SSCs that are the early precursors to sperm cells. They retrieved these cells from deceased human organ donors.
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Because SSCs already have the genes necessary to become embryonic stem cells, it is not necessary to add any new genes to coax them to morph into these progenitor cells, Gallicano says. "These are male germ cells as well as adult stem cells."
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"We found that once you take these cells out of the testes niche, they get confused, and will form all three germ layers within several weeks," he says. "These are true, pluripotent stem cells."
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& z& Y) ~0 k( ^# FThe research team took 1 gram of tissue from human testes and produced about 1 million stem cells in the laboratory. These cells showed many of the biological markers that characterize normal beta islet cells., b) _7 h8 i' N# L5 d* V& a1 G

) m: Q( j: i) H, n* ?2 Y# FThey then transplanted those cells into the back of immune deficient diabetic mice, and were able to decrease glucose levels in the mice for about a week -- demonstrating the cells were producing enough insulin to reduce hyperglycemia.
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While the effect lasted only week, Gallicano says newer research has shown the yield can be substantially increased.
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The research was funded in part by the American Diabetes Association, patient contributions to the GUMC Office of Advancement, support from GUMC diabetes specialist Stephen Clement, M.D., and a grant from GUMC.  b( v, y+ T6 J1 Z( d

& m6 |' y8 ^: u3 K+ gCo-authors include Anirudh Saraswathula, a student at Thomas Jefferson High School for Science and Technology in Alexandria, Va. GUMC researchers Shenglin Chen Ph.D., Stephen Clement, M.D., Martin Dym, Ph.D., and Asif Zakaria, Ph.D., also contributed to the research. The authors report having no personal financial interests related to the study./ v0 `: t" a* F6 q
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