Guttentag S H, Phelps D S, Stenzel W, Warshaw J B, Floros J
Department of Pediatrics, Harvard Medical School, Boston, Massachusetts 02115.
Am J Physiol. 1992 Apr;262(4 Pt 1):L489-94. doi: 10.1152/ajplung.1992.262.4.L489.
The content and distribution of the 26-to 38-kDa surfactant protein (SP-A) and its mRNA were determined in fetuses of control and streptozotocin (STZ)-treated Sprague-Dawley rats using immunohistochemistry, RNA blotting, and in situ hybridization. Female rats were treated with 50 mg/kg STZ before mating, and the fetuses were killed at fetal days 18-21 or on neonatal days 1 and 2 (day of birth = end of day 22). SP-A was barely detectable on fetal day 18 in controls and easily detected by fetal day 21. In the STZ group, SP-A was decreased compared with controls at fetal days 18-21. However, by neonatal days 1-2, there were no significant differences in SP-A levels between groups. SP-A mRNA was detectable at fetal day 18 in controls, but it was decreased in the STZ group at day 18-21 (P less than 0.02) and differences were no longer detected by neonatal days 1-2. SP-A and SP-A mRNA accumulated with advancing gestational age in both groups until neonatal days 1-2. The differences in SP-A and SP-A mRNA levels in the two groups diminished with advancing age but remained significant at fetal day 21. These data suggest that STZ-induced diabetes interferes with normal expression of SP-A in the developing fetal lung.
使用免疫组织化学、RNA印迹法和原位杂交技术,测定对照和链脲佐菌素(STZ)处理的Sprague-Dawley大鼠胎儿中26至38 kDa表面活性蛋白(SP-A)及其mRNA的含量和分布。雌性大鼠在交配前用50 mg/kg STZ处理,胎儿在胎龄18至21天或出生后第1天和第2天(出生日=第22天结束)处死。对照组在胎龄18天时几乎检测不到SP-A,到胎龄21天时则易于检测到。在STZ组中,胎龄18至21天时SP-A水平低于对照组。然而,到出生后第1至2天,两组间SP-A水平无显著差异。对照组在胎龄18天时可检测到SP-A mRNA,但在STZ组中,胎龄18至21天时其水平降低(P<0.02),到出生后第1至2天差异不再明显。两组中SP-A和SP-A mRNA均随胎龄增加而积累,直至出生后第1至2天。两组中SP-A和SP-A mRNA水平的差异随年龄增长而减小,但在胎龄21天时仍很显著。这些数据表明,STZ诱导的糖尿病会干扰发育中胎儿肺内SP-A的正常表达。