干细胞在大鼠出生后发育时期子宫组织存在的研究

Betül YALÇIN, Arzu Hanım YAY, Saim ÖZDAMAR
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引用次数: 0

摘要

子宫组织是一个具有高度增殖能力的器官,具有再生、分化和脱落的功能 是见过。虽然这种组织每个月都会再生,但其来源尚未确定。研究是# x0D;干细胞作为子宫内膜再生的来源和所表达的标记物进行了研究 通过这些细胞。本研究的目的是检测essential表达的CD9和CD13的免疫反应性;在出生后发育的各个阶段子宫和造血干细胞标志物CD34的数量[j];转运。本研究选用42只雌性wistar -白化大鼠,分为6组;组我;新生儿(2天),II组; 发情期(38天),第三组:可育期(12周),通过确定大鼠的发情周期阶段a) pro- 发情,b)发情,c)发情,d)发情。CD9、CD13、CD34在子宫组织中的表达对大鼠进行调查。在38天和12周的各组中,cd34表达细胞存在于细胞间质中;子宫内膜靠近子宫肌层,但在2天组中没有这种细胞。各组子宫上皮 除第2天组外,其余均有CD9表达。表达CD13的子宫内膜间质细胞仅显示少量 CD13在第12周组有明显表达。人们认为 在骨髓源性干细胞的作用下,青春期和成年期子宫内膜可再生;干细胞和子宫来源的上皮细胞和基质细胞。
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Investigation of the Presence of Stem Cells in Rat Uterus Tissue in Postnatal Development Periods
Uterine tissue is an organ with a high proliferation capacity where regeneration, differentiation and shedding are seen. Although this tissue is regenerated every month, the source of it hasn’t been determined yet. Studies are carried out on stem cells being a source that can provide regeneration of the endometrium and the markers expressed by these cells. The purpose of this study was to examine the immunreactivity of CD9 and CD13 expressed by essential population of uterus and CD34, marker of hematopoietic stem cells, at various stages of the postnatal developing pro- cess. In this study, was used 42 female Wistar-albino rats split into six groups; Group I; newborn (2-days), Group II; pubertal (38-days), and Group III: fertile group (12 weeks), by identifying the stages of the estrous cycle in rats a) pro- estrus, b) estrus, c) metestrus, d) diestrus. The expression of CD9, CD13, and CD34 in uterine tissues excised from rats was investigated. In the groups of 38-days and 12-weeks, CD34-expressing cells were present in the stroma of the endometrium next to the myometrium, but such cells were absent in the 2-days group. All groups' uterine epithelium displayed CD9 expression, except for group 2-days. Endometrial stromal cells that expressed CD13 showed only little immureactivity in groups 2 and 38-days, while CD13 expression is noticeable in group 12-weeks. It was thought that the uterine endometrium could be regenerated in puberty and adulthood with the contribution of bone marrow-derived stem cells and uterine-derived epithelial and stromal cells.
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