Cells cultured from the growing tip of red deer antler express alkaline phosphatase and proliferate in response to insulin-like growth factor-I
Cells cultured from the growing tip of red deer antler express alkaline phosphatase and proliferate in response to insulin-like growth factor-I
Deer antler growth provides a unique natural model of rapid and complete bone regeneration. In this study, the distal antler tips of male red deer (Cervus elaphus) were collected post-mortem during the annual growth period (April-August), and an in vitro system established for the culture of cells from three regions; the inner layer of the perichondrium, the reserve mesenchyme and the cartilage zone. Alkaline phosphatase (ALP) expression by cultured cells, as demonstrated by enzyme histochemistry and biochemical assay, reflected the stage of cellular differentiation. ALP activity was highest in cells cultured from the hypertrophic cartilage region (3.6 +/- 0.2 mumol/micrograms cell protein/minute), and lowest in undifferentiated mesenchymal cells (0.3 +/- 0.01 mumol/microgram cell protein/minute). ALP expression was lost with passage in culture. Levels of ALP activity in cultured cells correlated with the pattern and extent of enzyme expression in tissue sections as demonstrated by histochemical staining. Insulin-like growth factor (IGF)-I (10(-9)M-10(-7)M) was found to be mitogenic for cultured cells from all three zones as shown by increased incorporation of [3H]thymidine into DNA. These results demonstrate that cells from three different regions of the antler tip can be maintained in culture, and that antler cells share certain phenotypic characteristics of growth plate chondrocytes. These data provide further evidence of a role for IGF-1 in the regulation of antler growth. Antler regrowth is a potentially useful model for the study of the factors that regulate bone formation.
R9-R16
Price, J.S.
275074bf-843a-4b2b-b871-33e5a0b71a69
Oyajobi, B.O.
e2b53662-4ea3-485d-b669-9d6aebe6b5ec
Oreffo, R.O.
ff9fff72-6855-4d0f-bfb2-311d0e8f3778
Russell, R.G.
56578353-52d3-4bb5-9063-a915e86e95c8
November 1994
Price, J.S.
275074bf-843a-4b2b-b871-33e5a0b71a69
Oyajobi, B.O.
e2b53662-4ea3-485d-b669-9d6aebe6b5ec
Oreffo, R.O.
ff9fff72-6855-4d0f-bfb2-311d0e8f3778
Russell, R.G.
56578353-52d3-4bb5-9063-a915e86e95c8
Price, J.S., Oyajobi, B.O., Oreffo, R.O. and Russell, R.G.
(1994)
Cells cultured from the growing tip of red deer antler express alkaline phosphatase and proliferate in response to insulin-like growth factor-I.
Journal of Endocrinology, 143 (2), .
(PMID:7829985)
Abstract
Deer antler growth provides a unique natural model of rapid and complete bone regeneration. In this study, the distal antler tips of male red deer (Cervus elaphus) were collected post-mortem during the annual growth period (April-August), and an in vitro system established for the culture of cells from three regions; the inner layer of the perichondrium, the reserve mesenchyme and the cartilage zone. Alkaline phosphatase (ALP) expression by cultured cells, as demonstrated by enzyme histochemistry and biochemical assay, reflected the stage of cellular differentiation. ALP activity was highest in cells cultured from the hypertrophic cartilage region (3.6 +/- 0.2 mumol/micrograms cell protein/minute), and lowest in undifferentiated mesenchymal cells (0.3 +/- 0.01 mumol/microgram cell protein/minute). ALP expression was lost with passage in culture. Levels of ALP activity in cultured cells correlated with the pattern and extent of enzyme expression in tissue sections as demonstrated by histochemical staining. Insulin-like growth factor (IGF)-I (10(-9)M-10(-7)M) was found to be mitogenic for cultured cells from all three zones as shown by increased incorporation of [3H]thymidine into DNA. These results demonstrate that cells from three different regions of the antler tip can be maintained in culture, and that antler cells share certain phenotypic characteristics of growth plate chondrocytes. These data provide further evidence of a role for IGF-1 in the regulation of antler growth. Antler regrowth is a potentially useful model for the study of the factors that regulate bone formation.
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Published date: November 1994
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Human Development & Health
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Local EPrints ID: 360856
URI: http://eprints.soton.ac.uk/id/eprint/360856
PURE UUID: bbf32dd9-825b-4435-8b5a-4ce7f41ab71b
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Date deposited: 08 Jan 2014 17:02
Last modified: 11 Dec 2021 03:33
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Author:
J.S. Price
Author:
B.O. Oyajobi
Author:
R.G. Russell
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