Literature DB >> 23629696

Ischemic culture of dental pulp-derived cells is a useful model in which to investigate mechanisms of post-ischemic tissue recovery.

Hideki Agata1, Yoshinori Sumita, Izumi Asahina, Arinobu Tojo, Hideaki Kagami.   

Abstract

Dental pulp is a soft tissue characterized by unique regenerative properties. It is located in the center of each tooth, and is surrounded by hard tissue (dentin). Vascular access is limited to a small foramen at the root apex. Because of this anatomical limitation, dental pulp can easily lose its blood supply, causing the tissue to become ischemic. This occurs, for example, when a tooth is dislocated by traumatic injury or is subjected to inflammation. Since ischemia is caused by a critical shortage of oxygen and nutrients, ischemic damage is usually irreversible, even when the ischemic event is transient. However, unlike ischemia-sensitive organs such as the brain and heart, dental pulp is relatively ischemia-resistant, and recovers from ischemic injury by regenerating damaged tissue. The mechanisms by which this regeneration occurs are poorly understood, but are being investigated in cell culture models that mimic in vivo ischemic conditions using a combination of hypoxia and nutrient deprivation. Here, we review the use of ischemic cell culture to investigate the mechanisms of post-ischemic dental pulp tissue recovery.

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Year:  2013        PMID: 23629696     DOI: 10.14670/HH-28.985

Source DB:  PubMed          Journal:  Histol Histopathol        ISSN: 0213-3911            Impact factor:   2.303


  3 in total

1.  Coculture of stem cells from apical papilla and human umbilical vein endothelial cell under hypoxia increases the formation of three-dimensional vessel-like structures in vitro.

Authors:  Changyong Yuan; Penglai Wang; Lifang Zhu; Waruna Lakmal Dissanayaka; David William Green; Edith H Y Tong; Lijian Jin; Chengfei Zhang
Journal:  Tissue Eng Part A       Date:  2014-12-23       Impact factor: 3.845

2.  Do hypoxia and L-mimosine modulate sclerostin and dickkopf-1 production in human dental pulp-derived cells? Insights from monolayer, spheroid and tooth slice cultures.

Authors:  Klara Janjić; Barbara Cvikl; Christoph Kurzmann; Andreas Moritz; Hermann Agis
Journal:  BMC Oral Health       Date:  2018-03-09       Impact factor: 2.757

3.  The Influence of Pro-Inflammatory Factors on Sclerostin and Dickkopf-1 Production in Human Dental Pulp Cells Under Hypoxic Conditions.

Authors:  Klara Janjić; Mohammad Samiei; Andreas Moritz; Hermann Agis
Journal:  Front Bioeng Biotechnol       Date:  2019-12-17
  3 in total

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