Hua Zhang's research while affiliated with Nanjing University of Traditional Chinese Medicine and other places

What is this page?


This page lists the scientific contributions of an author, who either does not have a ResearchGate profile, or has not yet added these contributions to their profile.

It was automatically created by ResearchGate to create a record of this author's body of work. We create such pages to advance our goal of creating and maintaining the most comprehensive scientific repository possible. In doing so, we process publicly available (personal) data relating to the author as a member of the scientific community.

If you're a ResearchGate member, you can follow this page to keep up with this author's work.

If you are this author, and you don't want us to display this page anymore, please let us know.

Publications (1)


Fig. 3. PC treatment activated BMP/WNT signaling pathways. PC treatment increased gene expression of Bmps, Wnts and Runx2 (A), protein expression of p-Smad1/5/8,-Catenin and Runx2 (B). BMP antagonist Noggin and WNT inhibitor Dkk-1 pretreatment significantly attenuated PC-mediated (1.25 M) ALP activity (C) and mineralization (D), as well as the protein expression (E). Data were expressed as mean ± SD (n = 3). # p < 0.05 vs PC alone; *p < 0.05, **p < 0.01 vs control. Samples were measured in triplicate and experiments were repeated three times.
Fig. 4. PC-induced osteoblast differentiation was regulated by cAMP/cGMP pathways. cAMP inhibitor H89 (10 M) and cGMP inhibitor KT5832 (3 M) pretreatment significantly counteracted PC-mediated (1.25 M) ALP activity (A) and mineralization (B), as well as the protein expression (C). Data were expressed as mean ± SD (n = 3). # p < 0.05 vs PC alone; *p < 0.05, **p < 0.01 vs control. Samples were measured in triplicate and experiments were repeated three times.
(2 R ,3 S )-Pinobanksin-3-cinnamate promotes osteoblast differentiation through cAMP and cGMP pathways
  • Article
  • Full-text available

June 2018

·

55 Reads

·

3 Citations

Revista Brasileira de Farmacognosia

Hua Zhang

·

Guo-Peng Zhang

·

Hong Jiang

·

Zheng-Feng Gong

Flavones have the potential of being used as a dietary supplement for bone health promotion beyond calcium and vitamin D. Recent studies have showed that flavones enhanced bone formation and inhibited bone resorption by affecting osteoblast and osteoclast differentiation through various cell signaling pathways. In this study, we investigated the effects of a new flavone (2R,3S)-pinobanksin-3-cinnamate, isolated from the metabolites of the endophytic fungus Penicillium sp. FJ-1 of Acanthus ilicifolius L., Acanthaceae, on osteoblast differentiation by using MC3T3-E1 cells. It was observed that (2R,3S)-pinobanksin-3-cinnamate promoted osteoblast differentiation, as evidenced by increased mineralization process and alkaline phosphatase activity, as well as expression of genes encoding the bone differentiation. Moreover (2R,3S)-pinobanksin-3-cinnamate treatment upregulated the gene expression of wingless-type MMTV integration site family, bone morphogenetic protein and runt-related transcription factor 2, and protein expression of phosphor-Smad1/5/8, β-catenin and runt-related transcription factor 2 in MC3T3-E1 cells. The osteoblast differentiation effects induced by (2R,3S)-pinobanksin-3-cinnamate were attenuated by the bone morphogenetic protein antagonist Noggin, and wingless-type MMTV integration site family signaling pathway inhibitors Dickkopf-1. Co-treatment with adenosine 30,50-cyclic monophosphate and guanosine 30,50-cyclic monophosphate pathway inhibitors, H89 and KT5823, respectively, reversed the (2R,3S)-pinobanksin-3-cinnamate-induced activations of p-Smad1/5/8, β-catenin, and runt-related transcription factor 2. Our data demonstrated that (2R,3S)-pinobanksin-3-cinnamate promoted the osteoblast differentiation of MC3T3-E1 cells, at least partially through the adenosine 30,50-cyclic monophosphate and guanosine 30,50-cyclic monophosphate signaling pathways, providing the scientific rational to develop (2R,3S)-pinobanksin-3-cinnamate against bone loss-associated diseases.

Download
Share

Citations (1)


... Adenosine 30,50-cyclic monophosphate (cAMP) and guanosine 30,50-cyclic monophosphate (cGMP) signaling pathways have an opposite effect on cell proliferation and differentiation. Zhang et al. (50) found that the elevation of intracellular cAMP could enhance bone morphogenetic protein (BMP) action and increase the ALP activity of osteoblastic cells in experimental animals. Therefore, the long-term proliferation-promoting effect of MGF may attribute to the concentration of intracellular cAMP being lower than cGMP. ...

Reference:

Identification of Di/Tripeptide(s) With Osteoblasts Proliferation Stimulation Abilities of Yak Bone Collagen by in silico Screening and Molecular Docking
(2 R ,3 S )-Pinobanksin-3-cinnamate promotes osteoblast differentiation through cAMP and cGMP pathways

Revista Brasileira de Farmacognosia