Gaino E, Magnino G
Istituto di Zoologia, Perugia, Italy.
Microsc Res Tech. 1999 Feb 15;44(4):279-92. doi: 10.1002/(SICI)1097-0029(19990215)44:4<279::AID-JEMT7>3.0.CO;2-E.
The study of cell-cell and cell-substratum adhesion in vitro is useful for understanding cell behavior in a three-dimensional pattern. We have used dissociated cells (choanocytes represent the main fraction) from the calcareous sponge Clathrina, namely C. cerebrum and C. clathrus, to illustrate our present understanding on three main aspects of cell-cell and cell-substratum adhesion in vitro: (1) cytoskeletal protrusions; (2) cell behaviours on organic substrata; and (3) paths of locomotory sponge cell. Cell locomotion occurs by the extensions of scleropodial and lamellipodial protrusions, by way of actin polymerization. The extent to which cells produce these cytoplasmic processes varies according to the substratum (e.g., collagen, fibronectin, laminin, polylysine). It was found that more cell extensions were produced on collagen substrata, and this led to greater cell movement. Advancing choanocytes are not polarized. Their paths are particularly complicated, showing linear segments, which produce a more efficent cellular translocation, and winding tracts with frequent turns or loops. Small amoeboid cells describe more linear paths with a wide range of speed variation than larger cells. The presence of cell-derived substratum reduces the progressive dispersion of cells and allows cells to encounter one another in such a way that the initial random walking later turns into non-random displacement. Even though cAMP-treated cells exhibit different aggregative tactics, cAMP 10(-8) M remarkably enhances cell encounters and supports the existing information that this cyclic nucleotide represents a signal that affects cell morphology and locomotion. The bulk of data on sponge cell-cell and cell-substratum adhesion has been evaluated by mentioning the significant advances and references concerning studies of other cell systems.
体外细胞间和细胞与基质黏附的研究有助于理解细胞在三维模式下的行为。我们使用了来自钙质海绵Clathrina(即大脑海绵C. cerebrum和格子海绵C. clathrus)的解离细胞(领细胞占主要部分),来说明我们目前对体外细胞间和细胞与基质黏附三个主要方面的理解:(1)细胞骨架突起;(2)细胞在有机基质上的行为;(3)运动海绵细胞的路径。细胞运动通过硬化伪足和片状伪足突起的延伸,借助肌动蛋白聚合发生。细胞产生这些细胞质突起的程度因基质(如胶原蛋白、纤连蛋白、层粘连蛋白、聚赖氨酸)而异。研究发现,在胶原蛋白基质上产生的细胞突起更多,这导致细胞运动更剧烈。前进中的领细胞没有极性。它们的路径特别复杂,有直线段,能实现更有效的细胞移位,还有频繁转弯或成环的蜿蜒路径。小的变形细胞比大细胞描述的直线路径更多,速度变化范围更广。细胞衍生基质的存在减少了细胞的逐渐分散,使细胞能够相互接触,从而使最初的随机游动后来转变为非随机位移。尽管经cAMP处理的细胞表现出不同的聚集策略,但10(-8) M的cAMP显著增加了细胞间的接触,并支持了现有信息,即这种环核苷酸代表一种影响细胞形态和运动的信号。关于海绵细胞间和细胞与基质黏附的大量数据已通过提及其他细胞系统研究的重大进展和参考文献进行了评估。