Cytoskeletal/junction relationships during epithelial remodelling events

细胞表面是细胞与环境之间的界面。在这个界面上的相互作用使细胞能够产生运动，呈现特定的形状，执行特定的功能，并形成多细胞结构。赋予细胞形状并允许细胞移动的主要结构网络，即所谓的细胞骨架，与细胞表面有关，特别是与与邻近细胞和支持底物形成连接的表面区域有关，这或许并不令人惊讶。我的研究计划的长期目标是在组织的背景下探索细胞间连接和细胞内细胞骨架之间的相互作用，并确定这两个系统如何协同工作，在动物的许多管和腔中的细胞层(上皮)中产生复杂的重塑事件。我们特别感兴趣的是细胞骨架和连接如何相互作用，使细胞与相邻细胞分离，并通过上皮细胞从一个隔室移动到另一个隔室，或者从上皮细胞释放出来。在接下来的五年里，我们将探索细胞骨架和连接在哺乳动物睾丸生精上皮中移动发育中的精子细胞和释放完全形成的精子细胞的机制。在人类中，每天大约有8500万精子从每个睾丸的上皮中释放出来。我们将重点研究独特的细胞骨架相关结构，称为小管球复合体(TCS)，我们认为这是一种亚细胞机器，在精子细胞的产生和释放过程中发生的广泛的上皮重塑事件中，它内化并降解完整的细胞间连接。我们研究的一个方面是开发形成TCS的更完整的蛋白质目录。另一个是证明TCS的连接吞噬功能是允许发育早期的精子细胞在上皮内从一个区域移动到另一个区域所必需的。我们研究的更令人兴奋的方面之一将是确定细胞中的主要信号分子钙是否参与调节这些亚细胞机器的形成、结构和功能。我们的结果已经引起了生物学家对连接分解与精子释放相关的看法的范式转变。在接下来的几年里，我们预计我们的结果将产生类似的转变，生物学家如何看待下一代发育中的精子细胞在生精上皮中从一个隔室到另一个隔室的运动。重要的是，我们的研究将深入了解连接和连接周转是如何调节的，这可能有助于我们理解某些形式的男性不育的原因，并有助于我们确定开发男性避孕药的假定目标。

The cell surface is the interface between cells and their environment. Interactions at this interface enable cells to generate movement, to assume specific shapes, to carry out specific functions, and to form multicellular structures. It perhaps is not surprising that the major network of structures, the so-called cytoskeleton, that gives cells their shape and allows them to move is related to the cell surface, particularly to regions of the surface involved in forming connections both with neighboring cells and with supporting substrates. The long-term objective of my research program is to explore the interaction between intercellular junctions and the cytoskeleton in cells within the context of tissues, and determine how the two systems function together to generate complex remodeling events in cell layers (epithelia) that line the many tubes and cavities in animals. We are particularly interested in how the cytoskeleton and junctions interact to allow cells to detach from their neighbors and to move through epithelia from one compartment to another, or to be released from the epithelium. Over the next five years we will explore the mechanism by which the cytoskeleton and junctions function both to move developing sperm cells through the seminiferous epithelium of the mammalian testis and to release fully formed sperm cells. In humans, roughly 85 million sperm are released from the epithelium in each testis per day. We will focus our research on unique cytoskeleton-related structures termed tubulobulbar complexes (TCs)' that we propose are sub-cellular machines' that internalize and degrade intact intercellular junctions during the extensive epithelial remodeling events that occur during the production and release of sperm cells. One aspect of our study will be to develop a more complete catalogue of the proteins that form TCs. Another will be to show that the junction eating' function of TCs is necessary for allowing sperm cells in the early stages of their development to move from one region to another within the epithelium. One of the more exciting aspects of our study will be to determine if calcium, a major signaling molecule in cells, is involved in regulating the formation, structure and function of these subcellular machines. Our results have already generated a paradigm shift in how biologists view junction disassembly related to sperm release. Over the next few years we anticipate that our results will generate a similar shift in how biologist view the movement of the next generation of developing sperm cells from one compartment to another in the seminiferous epithelium. Importantly, our studies will provide insight into how the junctions and junction turnover are regulated which may contribute to our understanding of the causes of certain forms of male infertility, and to our identifying putative targets for the development of male contraceptives.