Butyrate-induced differentiation of PC12 cells to chromaffin cells involves cell adhesion and induction of extracellular proteins and cell adhesion proteins

Jee In Heoa; Soo Jin Oh; Yoon Jung Kho; Jeong hyeon Kim; Hong Joon Kang; Seong Hoon Park; Hyun Seok Kim; Jong Yeon Shin; Sung Young Lee; Min Ju Kim; Bon Hong Min; Sung Chan Kim; Jae Bong Park; Jaebong Kim; Jae Yong Lee

doi:10.1080/19768354.2010.528204

Butyrate-induced differentiation of PC12 cells to chromaffin cells involves cell adhesion and induction of extracellular proteins and cell adhesion proteins

Jee In Heoa, Soo Jin Oh, Yoon Jung Kho, Jeong hyeon Kim, Hong Joon Kang, Seong Hoon Park, Hyun Seok Kim, Jong Yeon Shin, Sung Young Lee, Min Ju Kim, Bon Hong Min, Sung Chan Kim, Jae Bong Park, Jaebong Kim, Jae Yong Lee

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3 Citations (Scopus)

Abstract

PC12 cells were differentiated into the cells of chromaffin phenotype by butyrate treatment. Cells were aggregated and formed tight cell adhesion. To investigate the molecular change in this differentiation, we examined expression levels of cell adhesion proteins and extracellular proteins during butyrate induced-differentiation of PC12 cells. Integrin β1, integrin α7, E cadherin, VCAM, collagen-I, fibronectin, desmoglein and connexin were increased during differentiation. The levels of clusterin and secreted clusterin were also increased. These increased levels of cell adhesion proteins and extracellular proteins appear to induce cell aggregation and tight cell adhesion. The levels of p21, p27 and p16 were increased probably because of differentiation-related growth arrest during differentiation. Prolonged incubation of butyrate up to 1 day was required for differentiation. Signal transduction pathways for this differentiatiom could not be identified since various inhibitors had no effect. The results showed that butyrateinduced differentiation of PC12 cells to chromaffin cells involves tight cell adhesion and induction of extracellular proteins and cell adhesion proteins.

Original language	English
Pages (from-to)	261-266
Number of pages	6
Journal	Animal Cells and Systems
Volume	14
Issue number	4
DOIs	https://doi.org/10.1080/19768354.2010.528204
Publication status	Published - 2010

Bibliographical note

Funding Information:
This work was supported by the Priority Research Centers Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2009-0094074).

Keywords

Butyrate
Cell adhesion proteins
Chromaffin cells
Differentiation
Pc12

ASJC Scopus subject areas

Animal Science and Zoology
General Biochemistry,Genetics and Molecular Biology

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10.1080/19768354.2010.528204

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Heoa, J. I., Oh, S. J., Kho, Y. J., Kim, J. H., Kang, H. J., Park, S. H., Kim, H. S., Shin, J. Y., Lee, S. Y., Kim, M. J., Min, B. H., Kim, S. C., Park, J. B., Kim, J., & Lee, J. Y. (2010). Butyrate-induced differentiation of PC12 cells to chromaffin cells involves cell adhesion and induction of extracellular proteins and cell adhesion proteins. Animal Cells and Systems, 14(4), 261-266. https://doi.org/10.1080/19768354.2010.528204

Heoa, JI, Oh, SJ, Kho, YJ, Kim, JH, Kang, HJ, Park, SH, Kim, HS, Shin, JY, Lee, SY, Kim, MJ, Min, BH, Kim, SC, Park, JB, Kim, J & Lee, JY 2010, 'Butyrate-induced differentiation of PC12 cells to chromaffin cells involves cell adhesion and induction of extracellular proteins and cell adhesion proteins', Animal Cells and Systems, vol. 14, no. 4, pp. 261-266. https://doi.org/10.1080/19768354.2010.528204

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abstract = "PC12 cells were differentiated into the cells of chromaffin phenotype by butyrate treatment. Cells were aggregated and formed tight cell adhesion. To investigate the molecular change in this differentiation, we examined expression levels of cell adhesion proteins and extracellular proteins during butyrate induced-differentiation of PC12 cells. Integrin β1, integrin α7, E cadherin, VCAM, collagen-I, fibronectin, desmoglein and connexin were increased during differentiation. The levels of clusterin and secreted clusterin were also increased. These increased levels of cell adhesion proteins and extracellular proteins appear to induce cell aggregation and tight cell adhesion. The levels of p21, p27 and p16 were increased probably because of differentiation-related growth arrest during differentiation. Prolonged incubation of butyrate up to 1 day was required for differentiation. Signal transduction pathways for this differentiatiom could not be identified since various inhibitors had no effect. The results showed that butyrateinduced differentiation of PC12 cells to chromaffin cells involves tight cell adhesion and induction of extracellular proteins and cell adhesion proteins.",

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note = "Funding Information: This work was supported by the Priority Research Centers Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2009-0094074).",

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AU - Heoa, Jee In

AU - Oh, Soo Jin

AU - Kho, Yoon Jung

AU - Kim, Jeong hyeon

AU - Kang, Hong Joon

AU - Park, Seong Hoon

AU - Kim, Hyun Seok

AU - Shin, Jong Yeon

AU - Lee, Sung Young

AU - Kim, Min Ju

AU - Min, Bon Hong

AU - Kim, Sung Chan

AU - Park, Jae Bong

AU - Kim, Jaebong

AU - Lee, Jae Yong

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PY - 2010

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N2 - PC12 cells were differentiated into the cells of chromaffin phenotype by butyrate treatment. Cells were aggregated and formed tight cell adhesion. To investigate the molecular change in this differentiation, we examined expression levels of cell adhesion proteins and extracellular proteins during butyrate induced-differentiation of PC12 cells. Integrin β1, integrin α7, E cadherin, VCAM, collagen-I, fibronectin, desmoglein and connexin were increased during differentiation. The levels of clusterin and secreted clusterin were also increased. These increased levels of cell adhesion proteins and extracellular proteins appear to induce cell aggregation and tight cell adhesion. The levels of p21, p27 and p16 were increased probably because of differentiation-related growth arrest during differentiation. Prolonged incubation of butyrate up to 1 day was required for differentiation. Signal transduction pathways for this differentiatiom could not be identified since various inhibitors had no effect. The results showed that butyrateinduced differentiation of PC12 cells to chromaffin cells involves tight cell adhesion and induction of extracellular proteins and cell adhesion proteins.

AB - PC12 cells were differentiated into the cells of chromaffin phenotype by butyrate treatment. Cells were aggregated and formed tight cell adhesion. To investigate the molecular change in this differentiation, we examined expression levels of cell adhesion proteins and extracellular proteins during butyrate induced-differentiation of PC12 cells. Integrin β1, integrin α7, E cadherin, VCAM, collagen-I, fibronectin, desmoglein and connexin were increased during differentiation. The levels of clusterin and secreted clusterin were also increased. These increased levels of cell adhesion proteins and extracellular proteins appear to induce cell aggregation and tight cell adhesion. The levels of p21, p27 and p16 were increased probably because of differentiation-related growth arrest during differentiation. Prolonged incubation of butyrate up to 1 day was required for differentiation. Signal transduction pathways for this differentiatiom could not be identified since various inhibitors had no effect. The results showed that butyrateinduced differentiation of PC12 cells to chromaffin cells involves tight cell adhesion and induction of extracellular proteins and cell adhesion proteins.

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Butyrate-induced differentiation of PC12 cells to chromaffin cells involves cell adhesion and induction of extracellular proteins and cell adhesion proteins

Abstract

Bibliographical note

Keywords

ASJC Scopus subject areas

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