Greengard O, Federman M, Knox W E
J Cell Biol. 1972 Feb;52(2):261-72. doi: 10.1083/jcb.52.2.261.
Quantitative stereological methods have been adapted for the measurement of the volume of liver attributable to parenchymal, hematopoietic, and Kupffer cells and for the measurement of the relative and absolute number (per unit volume) of these cell types and the mean volume of the parenchymal cell. These morphological parameters are the main ones for interpreting the biochemical differentiation of liver. Quantitative changes in these parameters, in rat liver between the 15th day of gestation and adult life, are presented. Despite the large number of hematopoietic cells, the parenchymal cells fill more than half of the liver volume between the 15th and 18th days of gestation and 0.85 of the liver volume at term. The fraction of liver volume occupied by Kupffer cells is never more than 0.02; the number of Kupffer cells per cubic centimeter increases less than twofold between fetal and adult life. The mean volume of individual parenchymal cells undergoes a threefold rise during late fetal life, declines in the neonatal period, and doubles between the 12th and 28th postnatal days. With the morphometric data obtained, it is impossible to convert enzyme concentrations (units per gram, determined in homogenates of whole liver) to enzyme amounts per unit volume of parenchymal or hematopoietic tissue or per individual cell of either type. In late fetal liver, only rises in enzyme concentration less than twofold may be attributed to the enrichment of parenchymal tissue at the expense of hematopoietic elements. The sudden upsurge, by more than twofold, of hepatic enzymes of the late fetal cluster (and also of the neonatal and late suckling cluster) reflects rises per parenchymal mass and per parenchymal cell. Thyroxine and glucagon, the administration of which to fetal rats promotes enzyme differentiation in liver, are without appreciable effect on the cytological parameters studied. Hydrocortisone accelerates the involution of hematopoietic tissue in fetal liver. Enzymes that are diminished by prenatal injection of hydrocortisone may be concentrated in hematopoietic cells.
定量体视学方法已被用于测量肝实质细胞、造血细胞和库普弗细胞所占肝脏的体积,以及这些细胞类型的相对和绝对数量(每单位体积)和实质细胞的平均体积。这些形态学参数是解释肝脏生化分化的主要参数。本文展示了大鼠肝脏从妊娠第15天到成年期这些参数的定量变化。尽管造血细胞数量众多,但在妊娠第15至18天,实质细胞占肝脏体积的一半以上,足月时占肝脏体积的0.85。库普弗细胞所占肝脏体积的比例从不超过0.02;每立方厘米库普弗细胞的数量在胎儿期到成年期增加不到两倍。单个实质细胞的平均体积在胎儿后期增加了两倍,在新生儿期下降,在出生后第12至28天翻倍。根据获得的形态学数据,无法将酶浓度(每克单位,在全肝匀浆中测定)转换为每单位体积实质或造血组织或每种类型单个细胞的酶量。在胎儿后期肝脏中,只有酶浓度增加不到两倍可能归因于以造血成分减少为代价的实质组织富集。胎儿后期簇(以及新生儿和哺乳后期簇)的肝酶突然激增两倍以上,反映了每单位实质质量和每个实质细胞的增加。给胎鼠注射甲状腺素和胰高血糖素可促进肝脏酶的分化,但对所研究的细胞学参数没有明显影响。氢化可的松加速胎儿肝脏造血组织的退化。产前注射氢化可的松后减少的酶可能集中在造血细胞中。