Cytoarchitectural features of Ucides cordatus (Crustacea Decapoda) hepatopancreas:: structure and elemental composition of electron-dense granules
Cytoarchitectural features of Ucides cordatus (Crustacea Decapoda) hepatopancreas:: structure and elemental composition of electron-dense granules
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DOI:
10.1016/s0040816602000101
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发表时间:
2002-10-01
期刊:
影响因子:
2.6
通讯作者:
Allodi, S
中科院分区:
文献类型:
--
作者:
Correa, JD;Farina, M;Allodi, S
Hepatopancreal tissue of the crab Ucides cordatus was investigated by light and electron microscopy. The observed epithelial cells were: E-cells (embryonic), located in the distal portion of the hepatopancreal tubules, R-cells (resorptive) F-cells (fibrillar) and B-cells (blister or secretory), found in its intermediate and proximal regions. Two types of electron-dense granules (EDGs) were found frequently in the cells of the proximal portion of the hepatopancreal tubule. Both types of EDGs presented alternating concentric electron-dense and electron-lucent layers. In order to better characterize these granules, energy dispersive X-ray analysis (EDXA) and glucose-6-phosphatase (G6Pase) cytochemistry were performed. One type of spherical granule was seen inside vacuoles surrounded by an association of myelin-like membranes as well as some small membrane-bound vesicles. This type of granule neither presented detectable Ca and P on EDXA spectra nor G6Pase cytochemical reaction products. The second type of granule had O, P and Ca characteristic peaks. G6Pase cytochemical products were observed inside these structures and showed that this mineralized type was surrounded by endloplasmic reticulum membranes. This result suggests that in U. cordatus the endoplasmic reticulum is associated with the genesis of mineralized EDGs. While amorphous mineral granules may be associated with a storage of Ca and P for the new carapace synthesis, EDGs covered by the nonmineralized spherical multi-layered membranes may be associated with late endosomes. No specific secretory pathway however was determined for the EDGs at the epithelial proximal portion. (C) 2002 Elsevier Science Ltd. All rights reserved.