Postnatal differentiation of the Golgi apparatus and the dendrites of Purkinje cells of the rat cerebellum

Summary The morphology of postnatal differentiation of the Golgi apparatus, the nucleus, the perikaryon, and the dendrites was studied in Purkinje cells of the rat cerebellum for 30 days after birth using histochemical, histological, and electron microscopic methods.The Golgi apparatus during differentiation undergoes morphological and positional changes. From the 1st to 7th postnatal day, the Golgi apparatus is found in a supranuclear position, and is connected with the axes of differentiating primary dendrites by beam-like processes. From days 8 to 11 this connection disappears, and most of the Golgi apparatus assumes a lateronuclear and infranuclear position. After the 11th or 12th day, the Golgi apparatus is found in perinuclear and peripheral cytoplasmic positions. The formation of granular endoplasmic reticulum occurs in the vicinity of the perinuclear Golgi apparatus. The differentiation of cell and nuclear forms requires approximately 20 days. The morphological changes of differentiation are discussed in relation to the participation of the Golgi apparatus in the differentiation of dendrites and in the formation of the granular endoplasmic reticulum.     

Stabilité du polymorphisme enzymatique dans les populations d''un Lépidoptère migrant,Agrotis ipsilon

Homogeneous population structure in a migrant Lepidoptera, Agrotis ipsilon. Light trapping of Agrotis ipsilon (Lepidoptera, Noctuidae) on various passes of the Alps and Pyrénées exhibited wide range movements between overwintering and aestivation areas. Electrophoretic analysis of samples taken in the Cantons of Vaud and Tessin (Switzerland), in the Rhône Delta (Southern France), and on passes of the Alps and Pyrénées, showed a great temporal and spatial homogeneity of allele frequencies (Fst values ranging from 0.002 to 0.013, and genetic distances from 0 to 0.004). These results support the hypothesis of a high level of gene flow. However, the occurrence during some years of high Fis values, might be explained by mixtures of populations that had undergone selection or went through a bottle-neck.     

EFFECTS OF VASOACTIVE INTESTINAL PEPTIDE ON ACTIVITIES OF SUCCINIC DEHYDROGENASE AND ALKALINE PHOSPHATASE IN RAT HEPATOMA CELLS

Using cytochemical method,microspectrophotometry and image analysis,effects of va-soactive intestinal peptide(VIP)on activities of succinic dehydrogenase(SDH)and alkalinephosphatase(ALP)in rat hepatoma cells were studied in vitro.The results showed that thehepatoma cell expressed potent positive reactions of SDH and ALP,the positive positionswere located at the cell membranes and/or cytoplasm.Having been treated with VIP,ALPdecreased obviously in activity(P<0. 01,compared with hepatoma cells untreated by VIP).The sites of ALP activty were chiefly located at the cell membranes,particularly at the cell-cell contacts.Cultured rat hepatoma cells had intensive SDH activity in their cytoplasm.Compared with untreated eclls,there was no marked difference in the intensity of SDH activ-ity in VIP-treated hepatoma cells(P>0.05).     

A STUDY OF GENUS MYCOPHILA FELT FROM CHINA (DIPTERA: CECIDOMYIIDAE)

Abstract  Three species of the genus Mycophila Felt collected from China are reported in this paper; M. speyeri Barnes 1926 from Jiangsu Province, M. longispina Bu et Mo sp. nov. from Shandong Province and M. echinoidea Bu et Mo sp. nov. from Sichuan Province are new to science. The type material of M. longispina Bu et Mo is deposited in the Department of Plant Protection, Shandong Agricultural University, Taian, Shandong, that of M. echinoidea Bu et Mo is deposited in the Department of Biology, Nankai University, Tianjin.     

Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locus.

Lipoprotein (a) (Lp[a]) is a cholesterol-rich lipoprotein resembling LDL but also containing a large polypeptide designated apolipoprotein (a) (apo[a]). Its levels are highly variable among individuals and, in a number of studies, are strongly correlated with the risk of coronary artery disease (CAD). In an effort to determine which genes control Lp(a) levels, we have studied 25 multiplex families (comprising 298 members) enriched for CAD. The apo(a) gene was genotyped among the families, using a highly informative pulse-field gel electrophoresis procedure. In addition, polymorphisms of the gene for the other major protein of Lp(a), apolipoprotein B (apoB), were examined. Quantitative sib-pair linkage analysis indicates that apo(a) is the major gene controlling Lp(a) levels in this CAD population (P = .001; 99 sib pairs), whereas the apoB gene demonstrated no significant quantitative linkage effect. We estimate that the apo(a) locus accounts for < or = 98% of variance of Lp(a) serum levels. Approximately 43% of this variation is explained by size polymorphisms within the apo(a) gene. These results indicate that the apo(a) gene is the major determinant of Lp(a) serum levels not only in the general population but also in a high-risk CAD population.