Tissue polarity in an insect segment: denticle patterns resemble spontaneously forming fibroblast patterns

Development ◽  
1987 ◽  
Vol 100 (1) ◽  
pp. 171-177 ◽  
Author(s):  
K. Nubler-Jung

The insect integument displays planar tissue polarity in the uniform posterior orientation of denticles and bristles. How do cell polarities become uniformly oriented in the plane of the epidermal sheet? We have already shown that it is possible to disturb uniform denticle orientation in abdominal segments of Dysdercus (Nubler- Jung, 1987). Here I report that abnormally oriented denticles tend to form small arrays with uniform orientation. Adjacent arrays with divergent orientations realize a small repertory of characteristic pattern elements. We obtain these pattern elements by orthogonal transformation of pattern elements that form spontaneously in confluent fibroblast cultures, which rely on autonomous cell behaviour, and which later simplify into patterns predicted by specific boundary conditions (Elsdale & Wasoff, 1976); the only additional parameter required is planar cell polarity. The abnormal patterns in Dysdercus may thus also form spontaneously and may also rely on autonomous cell behaviour. The normal pattern is predicted by the parallel segment boundaries. I propose that the characteristic pattern elements in the larval epidermis may arise because elongated epidermal cells tend to arrange in parallel arrays and to orient in the same direction. The normal posterior orientation of cell polarities may result from orienting cues provided by the anterior and by the posterior intersegmental regions.

2020 ◽  
Author(s):  
Fumiko Matsukawa Usami ◽  
Masaki Arata ◽  
Dongbo Shi ◽  
Sanae Oka ◽  
Yoko Higuchi ◽  
...  

SummaryThe molecular mechanisms by which cilia orientation is coordinated within and between multiciliated cells (MCCs) is not fully understood. By observing the orientation of basal bodies (BB) in MCCs of mouse oviducts, here, we show that Celsr1, a planar cell polarity (PCP) factor involved in tissue polarity regulation, is dispensable for determining BB orientation in individual cells, whereas CAMSAP3, a microtubule minus-end regulator, is critical for this process but not for PCP. MCCs exhibit a characteristic BB orientation and microtubule gradient along the tissue axis, and these intracellular polarities were maintained in the cells lacking Celsr1, although the intercellular coordination of the polarities was partly disrupted. On the other hand, CAMSAP3 regulated the assembly of microtubules interconnecting BBs by localizing at the BBs, and its mutation led to disruption of intracellular coordination of BB orientation, but not affecting PCP factor localization. Thus, both Celsr1 and CAMSAP3 are responsible for BB orientation but in distinct ways; and therefore, their cooperation should be critical for generating functional multiciliated tissues.


2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Gang Wu ◽  
Jiao Ge ◽  
Xupei Huang ◽  
Yimin Hua ◽  
Dezhi Mu

Congenital heart disease (CHD) is a common cardiac disorder in humans. Despite many advances in the understanding of CHD and the identification of many associated genes, the fundamental etiology for the majority of cases remains unclear. The planar cell polarity (PCP) signaling pathway, responsible for tissue polarity inDrosophilaand gastrulation movements and cardiogenesis in vertebrates, has been shown to play multiple roles during cardiac differentiation and development. The disrupted function of PCP signaling is connected to some CHDs. Here, we summarize our current understanding of how PCP factors affect the pathogenesis of CHD.


2011 ◽  
Vol 13 (8) ◽  
pp. 893-902 ◽  
Author(s):  
Danelle Devenport ◽  
Daniel Oristian ◽  
Evan Heller ◽  
Elaine Fuchs

Sign in / Sign up

Export Citation Format

Share Document