The ultrastructures of male meiocytes in tobacco, onion and lily were studied to elucidate the interaction between cytoplasmic channels (CCs) and plastids. Before meiosis, the male sporogenous cells had identically thickened cell walls (CWs) traversed by typical plasmodesmata (PDs). After entering meiosis, their CWs became uneven in thickness and 80-500nm aperture CCs were formed. Simultaneously, plastids or plastid-like bodies (PLBs) differing in size and morphology assembled at one or both ends of the CCs. These plastids and PLBs commonly orientated their sharper ends to face the CCs and were co-orientated on the axial line crossing the CC. Such pairs of plastids were often interconnected through the CC by thin (50-100nm) threads emanating from their membranes. Sometimes, plastids or PLBs extended directly from one side of a CW to the other, forming a bridge via the CC. In some cases, several plastids formed bridges between cells via one common CC. This is the first report that clearly demonstrates an intercellular continuum of, or communication between, plastids in male plant meiocytes.
To characterize the cytoplasmic structure reorganization during plant meiosis, the male meiocytes of Althaea rosea (L.) Cavan were examined under the combination of light and electron microscopy. Light microscopic observation of the toluidine blue-stained thick resin sections of young anthers revealed that the meiocytes of sporogenous cell stage were extremely voluminous and variable in shape and division plane. The cell walls (CWs) between some meiocytes were discontinuous at one or several site(s). These discontinuous portions varied between 0.2 and 3.0 microm in length. In addition, it was found that some meiocytes were able to produce protuberances that extended into another meiocyte. When transversally sectioned, the protuberance extending to another cell looked like a small cell lying in another cell. Transmission electron microscopy (TEM) showed that there were many long flat ER cisternae that were actively wrapping around a portion of cytoplasm in the male meiocytes at the sporogenous cell stage. During pre-meiosis interphase and early prophase I, a number of huge (0.5-1.0 microm diameter) spherical membrane-bound inclusions (MBIs) lined by single or double layer(s) of membrane were formed, each membrane actually representing one tightly appressed endoplasmic reticulum (ER) cisterna. The MBIs contained many granular, lamellar and fibrillar structures, and even small MBIs. Moreover, it was found that the MBIs could associate with the cytoplasmic channels (CCs) on CWs to release their contents into the cytoplasm of the opposite cell or directly extend from one cell to another through the CC. Taking all the data together, it is suggested that association of the MBIs and other organelles with CCs possibly functions in eliminating the non-identity of cytoplasm of the male meiocytes caused probably by the random asymmetric division observed at sporogenous cell phase, so as to ensure production of a large number of identical functional male gametes required for successful fertilization.
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