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Mol. Cells 2002; 13(2): 167-174

Published online January 1, 1970

© The Korean Society for Molecular and Cellular Biology

Dual Effect of Nerve Growth Factor on Cell Death of PC12 Cells Induced by Serum Deprivation

KyuChung Hur, Mijung Kwon, Sooryun Seo, Hoyoung Chun, Jun-Mo Chung, In Kwon Chung

Abstract

The effect of nerve growth factor (NGF) on the cell death of PC12 cells that is induced by serum depriva-tion was examined in the floating and attached cells to the extracellular matrix. NGF suppressed cell death occurred in the floating cells. The onset of cell death in the attached cells was much slower than in the floating cells. Moreover, the cell death in the attached cells was either accelerated in a high-density culture (over ~50% confluent), or inhibited in a low-density culture by NGF. While nucleosomal DNA fragmentation and poly (ADP-ribose) polymerase degradation was ob-served in both the floating and attached cells, the inci-dence of nuclear fragmentation and chromatin con-densation was much lower in the attached cells than in the floating cells. The delayed onset of cell death in the attached cells was due to the signals that are generated from the extracellular matrix that is formed by PC12 cells, together with cell-to-cell interaction. The accel-eration of cell death in the NGF-treated cells was anoikis, caused by the loss of the anchorage of the cell via the action of increased activities of matrix metallo-proteinases (MMP2, MMP9). These results suggest that NGF has a different role in the cell death of PC12 cells that is induced by serum deprivation, depending on the cell-matrix, as well as the cell-cell interaction.

Keywords Anoikis, Apoptosis, Matrix M, Extracellular Matrix

Article

Research Article

Mol. Cells 2002; 13(2): 167-174

Published online April 30, 2002

Copyright © The Korean Society for Molecular and Cellular Biology.

Dual Effect of Nerve Growth Factor on Cell Death of PC12 Cells Induced by Serum Deprivation

KyuChung Hur, Mijung Kwon, Sooryun Seo, Hoyoung Chun, Jun-Mo Chung, In Kwon Chung

Abstract

The effect of nerve growth factor (NGF) on the cell death of PC12 cells that is induced by serum depriva-tion was examined in the floating and attached cells to the extracellular matrix. NGF suppressed cell death occurred in the floating cells. The onset of cell death in the attached cells was much slower than in the floating cells. Moreover, the cell death in the attached cells was either accelerated in a high-density culture (over ~50% confluent), or inhibited in a low-density culture by NGF. While nucleosomal DNA fragmentation and poly (ADP-ribose) polymerase degradation was ob-served in both the floating and attached cells, the inci-dence of nuclear fragmentation and chromatin con-densation was much lower in the attached cells than in the floating cells. The delayed onset of cell death in the attached cells was due to the signals that are generated from the extracellular matrix that is formed by PC12 cells, together with cell-to-cell interaction. The accel-eration of cell death in the NGF-treated cells was anoikis, caused by the loss of the anchorage of the cell via the action of increased activities of matrix metallo-proteinases (MMP2, MMP9). These results suggest that NGF has a different role in the cell death of PC12 cells that is induced by serum deprivation, depending on the cell-matrix, as well as the cell-cell interaction.

Keywords: Anoikis, Apoptosis, Matrix M, Extracellular Matrix

Mol. Cells
Sep 30, 2023 Vol.46 No.9, pp. 527~572
COVER PICTURE
Chronic obstructive pulmonary disease (COPD) is marked by airspace enlargement (emphysema) and small airway fibrosis, leading to airflow obstruction and eventual respiratory failure. Shown is a microphotograph of hematoxylin and eosin (H&E)-stained histological sections of the enlarged alveoli as an indicator of emphysema. Piao et al. (pp. 558-572) demonstrate that recombinant human hyaluronan and proteoglycan link protein 1 (rhHAPLN1) significantly reduces the extended airspaces of the emphysematous alveoli by increasing the levels of TGF-β receptor I and SIRT1/6, as a previously unrecognized mechanism in human alveolar epithelial cells, and consequently mitigates COPD.

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