ABSTRACT
The germline cells in the ovary of the female bee are interconnected by intercellular bridges kept open by cytoskeletal reinforcements in the plasmic membrane. These bridges among the germline cells display a dynamic behavior and probably act in the determination of the oocyte among the cells of the clone formed by the premeiotic mitoses, subsequently forming a pathway that enables the products synthesized by the nurse cells to reach the oocyte during its maturation. The cytoskeletal elements in the intercellular bridges of bee gonads are basically microfilaments and microtubules, but another type of filament (thick, of non-defined nature, associated with elements of the endoplasmic reticulum) is present in the bridges between the premeiotic cystocytes. This filament crosses the bridge, using microfilaments to fasten itself to the plasmic membrane. These filaments appear to control the span of the bridge. Upon completion of the proliferation phase the cystocytes take on a rosette shape, and a fusome formed by the convergence of the bridges appears at their center. The thick filaments are not present in this conformation. The differentiation of the oocyte and the nurse cells leads to a new change, in which the bridges are reoriented to convey the content of the future nurse cells to the oocyte.
No ovário das abelhas as células germinativas e as células foliculares são interconectadas por pontes intercelulares mantidas abertas por reforços do citoesqueleto na membrana plasmática. As pontes entre as células germinativas têm comportamento dinâmico e provavelmente atuam na determinação do ovócito entre as células do clone formado pelas mitoses pré meióticas formando posteriormente uma via de transporte para que os produtos sintetizados pelas células nutridoras atinjam o ovócito durante sua maturação. Os elementos do citoesqueleto presentes nas pontes intercelulares das gônadas das abelhas são basicamente microfilamentos e microtúbulos, mas nas pontes entre os cistócitos pré-meióticos outro tipo de filamento (espesso de natureza não definida, associado a elementos do retículo endoplasmático) está presente, atravessando a ponte e prendendo-se através dos microfilamentos à membrana plasmática. Estes filamentos aparentemente controlam o vão da ponte. Terminada a fase de proliferação os cistócitos tomam a forma de uma roseta e um fusoma, formado pela convergência das pontes, aparece no centro desta. Nesta conformação os filamentos grossos não estão presentes. Nova mudança ocorre com a diferenciação do ovócito e das células nutridoras, com a reorientação de todas as pontes de maneira a canalizar o conteúdo das futuras células nutridoras para o ovócito.
ABSTRACT
Anopheles minimus collected from Yuanjiang, Yunnan Province, were bred with standard methods in lab. The ovarian nurse cells of A.minimus were separated and stained, and the whole polytene chromosomes were photographed under light microscope and compared with A.minimus from Guangxi. 365 samples of ovarian nurse cells were observed. The chromosomes included one telocentric sex-chromosome X, two submetacentric autosomes II(autosome II right arm, 2R and autosome II left arm, 2L) and two metacentric autosomes III(autosome III right arm, 3R, and autosome III left arm, 3L). The X is the shortest chromosome and the 2R is the longest one. In comparison with the pattern of polytene chromosomes of A. minimus from Guangxi, difference at 12 positions has been found at the parts of arms in banding sequences.