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  • Key words Atherosclerosis  (1)
  • mitochondria  (1)
  • Springer  (2)
  • 2000-2004
  • 1995-1999  (2)
  • 1
    ISSN: 1432-0878
    Keywords: Key words Atherosclerosis ; Culture model ; Endothelial cell ; Endothelin-1 ; Oxidized LDL ; Human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We investigated the structural and functional properties of human umbilical vein endothelial cells (HUVECs) cultured on a two-chamber culture model system using an amnion membrane. Compared to HUVECs cultured on a plastic dish, HUVECs cultured on the model system exhibited several features similar to those of in vivo vessels, including formation of the intercellular junctional devices and expression of tight junction-associated protein ZO-1 and adherence junction-associated protein α-catenin. Furthermore, we found that HUVECs had a property of polar secretion of endothelin-1 (ET-1). About 90% of the total amount of synthesized ET-1 was found in the lower well, designated as the basal side. When HUVECs were incubated with either native low-density lipoproteins (nLDLs) or oxidized LDLs (oxLDLs) at a concentration of 100 μg/ml, ET-1 secretion was significantly increased, dependent on the cell side (apical vs basal) on which the nLDLs or oxLDLs were loaded. When the LDLs were loaded on the apical side, the secretion of ET-1 from HUVECs on the apical side was increased by 48% (nLDL) and 61% (oxLDL), whereas it was accompanied by a concomitant decrease of ET-1 on the basal side (45% by nLDLs and 38% by oxLDLs). When loaded on the basal side, however, ET-1 was increased by 23% (nLDLs) and 53% (oxLDLs) on the basal side, with a 26% simultaneous decrease of ET-1 on the opposite side for both nLDLs and oxLDLs. On the contrary, high-density lipoproteins (HDLs) inhibited ET-1 secretion from HUVECs on the opposite side of the well on which HDLs were loaded; there was a 57% decrease on the basal side when HDLs were loaded on the apical side, and a 46% decrease on the apical side when loaded on the basal side. These results indicate that modulation of ET-1 secretion from ECs by lipoproteins is virtually dependent on the place (apical vs basal) where these proteins are present. The finding that nLDLs and oxLDLs enhance ET-1 secretion by ECs in a polarized pattern suggests that ET-1 may be involved in pathophysiological processes such as atherogenesis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Biologia plantarum 41 (1998), S. 539-546 
    ISSN: 1573-8264
    Keywords: cytoplasm ; endoplasmatic reticulum ; ingrowth ; mitochondria ; nuclei ; vesicles ; Zea mays
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The most basal endosperm cells of maize (Zea mays L.) began differentiating into transfer cells in 10 days after pollination (DAP). The thickening and ingrowths forming in the transfer cell wall were slow during 10 and 15 DAP. There were many vesicles, silky and string ball objects in cytoplasm, and the number of mitochondria and rough endoplasm reticulum increased. After 15 DAP, the wall thickening and ingrowths forming in the transfer cells sped up. By 20 DAP, the transfer cell zone had developed, there appeared 65 - 70 rows of cells in width and 3 - 4 layers of cell in depth, the obvious cell wall ingrowths presented strong positive reaction with periodic acid Schiff's reagent. After 20 DAP, no significant change appeared in the shape and structure of the transfer cells, and the transfer cells entered function stage. In the mature kernels (53 DAP), the most basal transfer cells were filled with ingrowths, however, dense cytoplasm was also found in these cells. The nuclei had quite irregular shapes in these cells. Some transfer cells contained black grains and crystals. A black layer formed in the pericarp tissue adjacent to the transfer cell zone. Full development of endosperm transfer cells was important for reduction of kernel abortion and increase of kernel mass.
    Type of Medium: Electronic Resource
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