Abstract:
:We have examined the effects of constitutive expression of PTHrP on the growth and differentiation of populations of cells derived from a clonal chondrocytic cell line, CFK2. Cells were stably transfected with cDNA encoding either full-length, secretory PTHrP (CFK2P) or nonsecretory PTHrP (CFK2P-SS). In cultures of cells plated at low density, secretory PTHrP acted as a potent mitogen compared with nonsecretory PTHrP or exogenous PTHrP-(1-34), both of which stimulated only a minor increase in proliferation. In populations of control cells maintained postconfluent for several weeks, there was a dramatic increase in expression of mRNA for type II collagen, aggrecan, and link protein. Addition of exogenous PTHrP-(1-34) at a concentration of 10(-8) M to these cultures was ineffective in inhibiting this time-dependent increase in expression of matrix proteins. In contrast, populations of cells producing either secretory or nonsecretory forms of PTHrP, maintained over the same time period, demonstrated an almost complete inhibition of mRNA expression for matrix proteins. These observations demonstrate that PTHrP acts as a bifunctional modulator of chondrogenesis and that some of its biological activity is exerted via a mechanism distinct from the recognised signal transduction pathways linked to the PTH/PTHrP receptor.
journal_name
J Cell Physioljournal_title
Journal of cellular physiologyauthors
Henderson JE,He B,Goltzman D,Karaplis ACdoi
10.1002/(SICI)1097-4652(199610)169:1<33::AID-JCP4>subject
Has Abstractpub_date
1996-10-01 00:00:00pages
33-41issue
1eissn
0021-9541issn
1097-4652pii
10.1002/(SICI)1097-4652(199610)169:1<33::AID-JCP4>journal_volume
169pub_type
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