Cell renewal in the gills of the fish Barbus conchonius

1980 ◽  
Vol 58 (4) ◽  
pp. 650-653 ◽  
Author(s):  
Marlene MacKinnon ◽  
Hildegard E. Enesco

This radioautographic study established that the epithelial cells of the teleost gill have the cell division and cell migration patterns characteristic of a cell renewal system. [3H]Thymidine was injected into the small tropical fish Barbus conchonius, where it became incorporated into the newly synthesized DNA of dividing cells. Three fish were sacrificed at each of the following postinjection time intervals: 1, 12, 24, and 36 h. At 1 h, labeled nuclei were found only at the base of the gill filament, near the gill arch. At each successive time interval, labeled nuclei were found further out along the length of the gill filament. At later stages, labeled nuclei were also seen at the tips of the lamellae which project perpendicularly from the filaments. The number of labeled nuclei at the point of origin steadily declined with time. These data demonstrate that gill epithelial cells originate at the base of the gill arch and migrate both outward along the filament and upward along the lamellae. This pattern of cell division and cell migration demonstrates that the gill epithelium is a cell renewal system.

1993 ◽  
Vol 90 (24) ◽  
pp. 12030-12034 ◽  
Author(s):  
R. G. Faragher ◽  
I. R. Kill ◽  
J. A. Hunter ◽  
F. M. Pope ◽  
C. Tannock ◽  
...  
Keyword(s):  

2002 ◽  
Vol 23 (6) ◽  
pp. 1065-1070 ◽  
Author(s):  
Jenifer I. Fenton ◽  
Margaret S. Wolff ◽  
Michael W. Orth ◽  
Norman G. Hord

1989 ◽  
Vol 139 (2) ◽  
pp. 269-274 ◽  
Author(s):  
Heideh Fattaey ◽  
Terry C. Johnson ◽  
Hsin-Hwei Chou

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Masaya Hagiwara ◽  
Hisataka Maruyama ◽  
Masakazu Akiyama ◽  
Isabel Koh ◽  
Fumihito Arai

AbstractCollective migration of epithelial cells is a fundamental process in multicellular pattern formation. As they expand their territory, cells are exposed to various physical forces generated by cell–cell interactions and the surrounding microenvironment. While the physical stress applied by neighbouring cells has been well studied, little is known about how the niches that surround cells are spatio-temporally remodelled to regulate collective cell migration and pattern formation. Here, we analysed how the spatio-temporally remodelled extracellular matrix (ECM) alters the resistance force exerted on cells so that the cells can expand their territory. Multiple microfabrication techniques, optical tweezers, as well as mathematical models were employed to prove the simultaneous construction and breakage of ECM during cellular movement, and to show that this modification of the surrounding environment can guide cellular movement. Furthermore, by artificially remodelling the microenvironment, we showed that the directionality of collective cell migration, as well as the three-dimensional branch pattern formation of lung epithelial cells, can be controlled. Our results thus confirm that active remodelling of cellular microenvironment modulates the physical forces exerted on cells by the ECM, which contributes to the directionality of collective cell migration and consequently, pattern formation.


2010 ◽  
Vol 2010 ◽  
pp. 1-13 ◽  
Author(s):  
Fei Xue ◽  
Deanna M. Janzen ◽  
David A. Knecht

Numerous F-actin containing structures are involved in regulating protrusion of membrane at the leading edge of motile cells. We have investigated the structure and dynamics of filopodia as they relate to events at the leading edge and the function of the trailing actin networks. We have found that although filopodia contain parallel bundles of actin, they contain a surprisingly nonuniform spatial and temporal distribution of actin binding proteins. Along the length of the actin filaments in a single filopodium, the most distal portion contains primarily T-plastin, while the proximal portion is primarily bound byα-actinin and coronin. Some filopodia are stationary, but lateral filopodia move with respect to the leading edge. They appear to form a mechanical link between the actin polymerization network at the front of the cell and the myosin motor activity in the cell body. The direction of lateral filopodial movement is associated with the direction of cell migration. When lateral filopodia initiate from and move toward only one side of a cell, the cell will turn opposite to the direction of filopodial flow. Therefore, this filopodia-myosin II system allows actin polymerization driven protrusion forces and myosin II mediated contractile force to be mechanically coordinated.


2021 ◽  
Vol 17 (6) ◽  
pp. 1079-1087
Author(s):  
Zaozao Chen ◽  
Qiwei Li ◽  
Shihui Xu ◽  
Jun Ouyang ◽  
Hongmei Wei

Matrix nanotopography plays an essential role in regulating cell behaviors including cell proliferation, differentiation, and migration. While studies on isolated single cell migration along the nanostructural orientation have been reported for various cell types, there remains a lack of understanding of how nanotopography regulates the behavior of collectively migrating cells during processes such as epithelial wound healing. We demonstrated that collective migration of epithelial cells was promoted on nanogratings perpendicular to, but not on those parallel to, the wound-healing axis. We further discovered that nanograting-modulated epithelial migration was dominated by the adhesion turnover process, which was Rho-associated protein kinase activity-dependent, and the lamellipodia protrusion at the cell leading edge, which was Rac1-GTPase activity-dependent. This work provides explanations to the distinct migration behavior of epithelial cells on nanogratings, and indicates that the effect of nanotopographic modulations on cell migration is cell-type dependent and involves complex mechanisms


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