sustentacular cell
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2022 ◽  
pp. 030098582110691
Author(s):  
Nathan K. Hoggard ◽  
Linden E. Craig

Medullary bone is a calcium-rich, labile bone normally occurring in female birds with each egg-laying cycle. The stimulus for formation of medullary bone is, in part, the cyclic increase in serum estrogens produced by preovulatory ovarian follicles. Increased bone density due to formation of medullary bone, particularly in pneumatic bones, has been termed polyostotic hyperostosis, even if physiologic. This study investigated the formation of medullary bone in nonpneumatic (femur) and pneumatic (humerus) bones in sexually mature male budgerigars submitted for autopsy. Of the 21 sexually mature male budgerigars submitted for autopsy, 7 (33%) had medullary bone in 1 or more bones examined. All 7 male budgerigars with medullary bone had a testicular neoplasm, which was morphologically consistent with a testicular sustentacular cell tumor, seminoma, or interstitial cell tumor. Medullary bone was not present in the 14 cases with other diseases. Medullary bone formation in pneumatic and nonpneumatic bones can occur in male budgerigars with testicular neoplasms. Radiographic increases in medullary bone density, particularly in the humerus, could provide antemortem indication of testicular neoplasia in male budgerigars.


Genes ◽  
2020 ◽  
Vol 11 (5) ◽  
pp. 493 ◽  
Author(s):  
Fengyi Liang

The pseudostratified olfactory epithelium (OE) may histologically appear relatively simple, but the cytological relations among its cell types, especially those between olfactory receptor neurons (ORNs) and olfactory sustentacular cells (OSCs), prove more complex and variable than previously believed. Adding to the complexity is the short lifespan, persistent neurogenesis, and continuous rewiring of the ORNs. Contrary to the common belief that ORN dendrites are mostly positioned between OSCs, recent findings indicate a sustentacular cell enwrapped configuration for a majority of mature ORN dendrites at the superficial layer of the OE. After vertically sprouting out from the borderlines between OSCs, most of the immature ORN dendrites undergo a process of sideways migration and terminal maturation to become completely invaginated into and enwrapped by OSCs. Trailing the course of the dendritic sideways migration is the mesodendrite (mesentery of the enwrapped dendrite) made of closely apposed, cell junction connected plasma membrane layers of neighboring folds of the host sustentacular cell. Only a minority of the mature ORN dendrites at the OE apical surface are found at the borderlines between OSCs (unwrapped). Below I give a brief update on the cytoarchitectonic relations between the ORNs and OSCs of the OE. Emphasis is placed on the enwrapment of ORN dendrites by OSCs, on the sideways migration of immature ORN dendrites after emerging from the OE surface, and on the terminal maturation of the ORNs. Functional implications of ORN dendrite enwrapment and a comparison with myelination or Remak’s bundling of axons or axodendrites in the central and peripheral nervous system are also discussed.


2017 ◽  
Vol 114 (28) ◽  
pp. E5589-E5598 ◽  
Author(s):  
Daniel B. Herrick ◽  
Brian Lin ◽  
Jesse Peterson ◽  
Nikolai Schnittke ◽  
James E. Schwob

The remarkable capacity of the adult olfactory epithelium (OE) to regenerate fully both neurosensory and nonneuronal cell types after severe epithelial injury depends on life-long persistence of two stem cell populations: the horizontal basal cells (HBCs), which are quiescent and held in reserve, and mitotically active globose basal cells. It has recently been demonstrated that down-regulation of the ΔN form of the transcription factor p63 is both necessary and sufficient to release HBCs from dormancy. However, the mechanisms by which p63 is down-regulated after acute OE injury remain unknown. To identify the cellular source of potential signaling mechanisms, we assessed HBC activation after neuron-only and sustentacular cell death. We found that ablation of sustentacular cells is sufficient for HBC activation to multipotency. By expression analysis, next-generation sequencing, and immunohistochemical examination, down-regulation of Notch pathway signaling is coincident with HBC activation. Therefore, using HBC-specific conditional knockout of Notch receptors and overexpression of N1ICD, we show that Notch signaling maintains p63 levels and HBC dormancy, in contrast to its suppression of p63 expression in other tissues. Additionally, Notch1, but not Notch2, is required to maintain HBC dormancy after selective neuronal degeneration. Taken together, our data indicate that the activation of HBCs observed after tissue injury or sustentacular cell ablation is caused by the reduction/elimination of Notch signaling on HBCs; elimination of Jagged1 expressed by sustentacular cells may be the ligand responsible.


2016 ◽  
Vol 93 (1) ◽  
pp. 75-81
Author(s):  
Sawetree Pakkarato ◽  
Wipawee Thoungseabyoun ◽  
Apussara Tachow ◽  
Atsara Rawangwong ◽  
Yoshiteru Kagawa ◽  
...  

2013 ◽  
Vol 2 ◽  
pp. 129-135 ◽  
Author(s):  
Magdalena Białas ◽  
Krzysztof Okoń ◽  
Grzegorz Dyduch ◽  
Katarzyna Ciesielska-Milian ◽  
Monika Buziak ◽  
...  

2008 ◽  
Vol 314 (1) ◽  
pp. 40-58 ◽  
Author(s):  
Steve Rodriguez ◽  
Heather M. Sickles ◽  
Chris DeLeonardis ◽  
Ana Alcaraz ◽  
Thomas Gridley ◽  
...  

1997 ◽  
Vol 248 (3) ◽  
pp. 307-321 ◽  
Author(s):  
Sarah K. Pixley ◽  
Albert I. Farbman ◽  
Bert Ph. M. Menco

Author(s):  
Sarah K. Pixley ◽  
Marian Miller

When newborn rat olfactory mucosal cells were dissaggregated and plated as single cells onto astrocyte bed layers, abundant generation and maturation of olfactory receptor neurons was observed. Both immature and mature neurons were found in large multicellular spheres after 15 days in culture,. In sections of the spheres, almost all had central cavities, and the neurons were located almost exclusively in the external 1-2 cell layers. We show here that the spheres also contain olfactory sustentacular cells, neuronal supporting cells similar to retinal Muller cells. Sustentacular cell presence was shown by immunostaining cultured cells with a monoclonal antibody, SUS, which has previously been shown to recognize only sustentacular cells and a subset of the Bowman's gland cells. Fig. 1 shows that cultured cellular spheres contained numerous SUSpositive, roughly bipolar cells. These cells appear to be located internally rather than on the external surface. Sustentacular cell presence was further confirmed by immunostaining with a monoclonal antibody, 1F4, developed in this laboratory.


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