𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Dissociation between parathyroid hormone-stimulated cAMP and calcium increase in UMR-106-01 cells

✍ Scribed by Bradley S. Merritt; Dean T. Yamaguchi; Jacob Green; Charles R. Kleeman; Shmuel Muallem


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
987 KB
Volume
152
Category
Article
ISSN
0021-9541

No coin nor oath required. For personal study only.

✦ Synopsis


We used the osteogenic sarcoma cell line, UMR-106-01, to determine whether the rise in free cytosolic Ca2+ concentration ([Ca"],) and cellular cAMP following PTH stimulation are able to be regulated independently. For this purpose, we compared the effect of a PTH antagonist, stimulation of protein kinase C, augrnentation by prostaglandins, and the time course of desensitization of the two cellular responses. Two X M of the PTH antagonist '*"Nle '"Tyr-bPTH(3-34) arnide ([Nle,Tyr]hPTH(3-34)A) wa5 reqtiired to inhibit lopL' M bPTH(1-34)-stimulatcd cAMP generation by 50%. 1 0-7 M bPTH(1-34) completely overcame the inhibition induced by loph M 1Nle;ryr]bPTH(3-34)A. Only 7 x lo-" M and 2.7 x l o p 7 M [Nle,Tyr]bPTH(3-34)A were required to half maximally inhibit the D 1992 WILEY-LTSS, INC


πŸ“œ SIMILAR VOLUMES


Protein kinase C modulator effects on pa
✍ Michael Babich; Lisa R.P. Foti; Kevin L. Mathias πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 388 KB πŸ‘ 2 views

The effects of parathyroid hormone (PTH) on 1,4,5-inositol triphosphate (1,4,5-IP 3 ) and intracellular free calcium (Ca i 21 ) in osteoblasts are variable, whereas adenylate cyclase activity is consistently stimulated. Cyclic AMP is considered a mediator in the contractile effects of PTH on osteobl

1,25-dihydroxyvitamin D3 stimulated prot
✍ Ricky Cheung; Mary S. Erclik; Jane Mitchell πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 260 KB

## Abstract 1,25‐Dihydroxyvitamin D~3~ (1,25(OH)~2~D~3~) treatment of osteoblastic cells was shown previously to attenuate Parathyroid hormone (PTH) response by inhibiting adenylyl cyclase (AC) activity. In this study, we have investigated the mechanism by which 1,25(OH)~2~D~3~ inhibits AC in rat o