Apocrine hidrocystoma on the genitalia of a 9‐year‐old girl

Pediatric Dermatology, EarlyView.


https://ift.tt/2Hia1nG

Idiopathic facial aseptic granuloma—A diagnostic challenge in pediatric dermatology

Pediatric Dermatology, EarlyView.


https://ift.tt/2Esr4A2

A case of extensive acquired progressive lymphangioma

Pediatric Dermatology, EarlyView.


https://ift.tt/2Hi9z8Y

Occult dysraphism presenting with acro‐osteolysis

Pediatric Dermatology, EarlyView.


https://ift.tt/2Es0Uxm

Compound heterozygous mutations in desmoplakin associated with skin fragility, follicular hyperkeratosis, alopecia, and nail dystrophy

Pediatric Dermatology, EarlyView.


https://ift.tt/2Hi9qSY

Evidence‐based dosing of maintenance subcutaneous immunotherapy: a contemporary review of state‐of‐the‐art practice

International Forum of Allergy &Rhinology, EarlyView.


https://ift.tt/2qdWMwP

Hypoxia upregulates the expression of the pluripotency markers in the stem cells from human deciduous teeth

Abstract

Objectives

Cultivation under hypoxia promotes different responses in the mesenchymal stem cells and it has been producing promising results for clinical applications. Pulp tissue from deciduous teeth is a source of stem cells which has a high proliferative potential but this is usually discarded. This study has evaluated the effects of hypoxia on proliferation, apoptosis, and the expression of the pluripotency-related genes of the stem cells from human exfoliated deciduous teeth (SHED).

Materials and methods

The cells were isolated from dental pulp (n = 5) and characterized as mesenchymal stem cells, in accordance with the International Society for Cell Therapy. The cells were cultivated under hypoxia (3% oxygen) and compared to the normoxia cells (21% oxygen). The proliferation rate was evaluated by the Ki67 antibody for up to 7 days, while the metabolic activity was measured by the wst-8 assay for up to 14 days. The apoptotic cells were analyzed by Annexin V and propidium iodide staining at 24 h and 4 and 7 days. The expression of the pluripotent genes (OCT4, SOX2, and NANOG) was quantified by qPCR after 24 h, or 7 days, when cultivated under hypoxia or normoxia.

Results

No differences in the metabolic activity, the proliferation rate, and the apoptosis of SHED when cultivated under hypoxia or normoxia (p > 0.05) were observed. The expression of the pluripotent genes was significantly higher after 24 h and 7 days of the cells that were exposed to hypoxia (p < 0.01).

Conclusion

These findings have indicated an increase of the pluripotency-related genes within 7 days as being the main advantage of SHED culture under hypoxia.

Clinical relevance

Hypoxia culture may help maintain the quiescent state of the SHED, which could be advantageous for their future clinical applications.

https://ift.tt/2IvXRa3