Tsuji M, Shima H, Boutin E, Young P, Cunha G R
Department of Anatomy, University of California, San Francisco 94143.
J Androl. 1994 Nov-Dec;15(6):565-74.
To investigate the developmental properties of glandular mesenchymal inductors along the cranial-caudal extent of the developing male urogenital tract, neonatal mouse seminal vesicle epithelium (SVE) was combined with mesenchyme of the seminal vesicle (SVM), urogenital sinus (UGM), bulbourethral gland (BUG-M), or bladder (BLM) and grafted under the renal capsule of adult syngeneic or athymic male mice. Both SVM + SVE and UGM + SVE tissue recombinants expressed SV histogenesis and SV secretory proteins. BUG-M + SVE recombinants exhibited extensive growth as evidenced by a 36-fold increase in wet weight and a 27-fold increase in DNA content; however, the glandular structures that were induced in the SVE lacked the convoluted mucosa typical of SV. Furthermore, neither SV nor prostatic secretory proteins were detected in these recombinants. SVE grown in association with BLM failed to develop altogether. Thus, the ability to promote SV histogenesis and function is distinctly different in mesenchyme of cranial (SVM and UGM) versus caudal (BUG-M) regions. This implies the existence of a glandular inductive field in the developing male urogenital tract within which inductive activity varies regionally.
为了研究腺间充质诱导物在发育中的雄性泌尿生殖道头-尾方向上的发育特性,将新生小鼠精囊上皮(SVE)与精囊间充质(SVM)、泌尿生殖窦间充质(UGM)、尿道球腺间充质(BUG-M)或膀胱间充质(BLM)相结合,并移植到同基因或无胸腺成年雄性小鼠的肾被膜下。SVM + SVE和UGM + SVE组织重组体均表达精囊组织发生和精囊分泌蛋白。BUG-M + SVE重组体表现出广泛生长,湿重增加36倍,DNA含量增加27倍;然而,在SVE中诱导形成的腺结构缺乏精囊典型的卷曲黏膜。此外,在这些重组体中未检测到精囊或前列腺分泌蛋白。与BLM联合培养的SVE完全未能发育。因此,促进精囊组织发生和功能的能力在头侧(SVM和UGM)与尾侧(BUG-M)区域的间充质中明显不同。这意味着在发育中的雄性泌尿生殖道中存在一个腺诱导场,其中诱导活性存在区域差异。