Age-related changes in gap junctional intercellular communication in osteoblastic cells

Damian C Genetos, Zhiyi Zhou, Zhongyong Li, Henry J. Donahue

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Aging demonstrates deleterious effects upon the skeleton which can predispose an individual to osteoporosis and related fractures. Despite the well-documented evidence that aging decreases bone formation, there remains little understanding whereby cellular aging alters skeletal homeostasis. We, and others, have previously demonstrated that gap junctions-membrane-spanning channels that allow direct cell-to-cell conductance of small signaling molecules-are critically involved in osteoblast differentiation and skeletal homeostasis. We examined whether the capacity of rat osteoblastic cells to form gap junctions and respond to known modulators of gap junction intercellular communication (GJIC) was dependent on the age of the animal from which they were isolated. We observed no effect of age upon osteoblastic Cx43 mRNA, protein or GJIC. We also examined age-related changes in PTH-stimulated GJIC. PTH demonstrated age-dependent effects upon GJIC: Osteoblastic cells from young rats increased GJIC in response to PTH, whereas there was no change in GJIC in response to PTH in osteoblastic cells from mature or old rats. PTH-stimulated GJIC occurred independently of changes in Cx43 mRNA or protein expression. Cholera toxin significantly increased GJIC in osteoblastic cells from young rats compared to those from mature and old rats. These data demonstrate an age-related impairment in the capacity of osteoblastic cells to generate functional gap junctions in response to PTH, and suggest that an age-related defect in G protein-coupled adenylate cyclase activity at least partially contributes to decreased PTH-stimulated GJIC.

Original languageEnglish (US)
Pages (from-to)1979-1984
Number of pages6
JournalJournal of Orthopaedic Research
Volume30
Issue number12
DOIs
StatePublished - Dec 2012

Fingerprint

Gap Junctions
Connexin 43
Homeostasis
Messenger RNA
Connexins
Cell Aging
Cholera Toxin
Osteoblasts
Ion Channels
GTP-Binding Proteins
Adenylyl Cyclases
Osteogenesis
Skeleton
Cell Communication
Osteoporosis

Keywords

  • aging
  • connexion 43
  • gap junction
  • osteoblast
  • parathyroid hormone

ASJC Scopus subject areas

  • Orthopedics and Sports Medicine

Cite this

Age-related changes in gap junctional intercellular communication in osteoblastic cells. / Genetos, Damian C; Zhou, Zhiyi; Li, Zhongyong; Donahue, Henry J.

In: Journal of Orthopaedic Research, Vol. 30, No. 12, 12.2012, p. 1979-1984.

Research output: Contribution to journalArticle

Genetos, Damian C ; Zhou, Zhiyi ; Li, Zhongyong ; Donahue, Henry J. / Age-related changes in gap junctional intercellular communication in osteoblastic cells. In: Journal of Orthopaedic Research. 2012 ; Vol. 30, No. 12. pp. 1979-1984.
@article{605f8ae094f94020999ae151a06b01c7,
title = "Age-related changes in gap junctional intercellular communication in osteoblastic cells",
abstract = "Aging demonstrates deleterious effects upon the skeleton which can predispose an individual to osteoporosis and related fractures. Despite the well-documented evidence that aging decreases bone formation, there remains little understanding whereby cellular aging alters skeletal homeostasis. We, and others, have previously demonstrated that gap junctions-membrane-spanning channels that allow direct cell-to-cell conductance of small signaling molecules-are critically involved in osteoblast differentiation and skeletal homeostasis. We examined whether the capacity of rat osteoblastic cells to form gap junctions and respond to known modulators of gap junction intercellular communication (GJIC) was dependent on the age of the animal from which they were isolated. We observed no effect of age upon osteoblastic Cx43 mRNA, protein or GJIC. We also examined age-related changes in PTH-stimulated GJIC. PTH demonstrated age-dependent effects upon GJIC: Osteoblastic cells from young rats increased GJIC in response to PTH, whereas there was no change in GJIC in response to PTH in osteoblastic cells from mature or old rats. PTH-stimulated GJIC occurred independently of changes in Cx43 mRNA or protein expression. Cholera toxin significantly increased GJIC in osteoblastic cells from young rats compared to those from mature and old rats. These data demonstrate an age-related impairment in the capacity of osteoblastic cells to generate functional gap junctions in response to PTH, and suggest that an age-related defect in G protein-coupled adenylate cyclase activity at least partially contributes to decreased PTH-stimulated GJIC.",
keywords = "aging, connexion 43, gap junction, osteoblast, parathyroid hormone",
author = "Genetos, {Damian C} and Zhiyi Zhou and Zhongyong Li and Donahue, {Henry J.}",
year = "2012",
month = "12",
doi = "10.1002/jor.22172",
language = "English (US)",
volume = "30",
pages = "1979--1984",
journal = "Journal of Orthopaedic Research",
issn = "0736-0266",
publisher = "John Wiley and Sons Inc.",
number = "12",

}

TY - JOUR

T1 - Age-related changes in gap junctional intercellular communication in osteoblastic cells

AU - Genetos, Damian C

AU - Zhou, Zhiyi

AU - Li, Zhongyong

AU - Donahue, Henry J.

PY - 2012/12

Y1 - 2012/12

N2 - Aging demonstrates deleterious effects upon the skeleton which can predispose an individual to osteoporosis and related fractures. Despite the well-documented evidence that aging decreases bone formation, there remains little understanding whereby cellular aging alters skeletal homeostasis. We, and others, have previously demonstrated that gap junctions-membrane-spanning channels that allow direct cell-to-cell conductance of small signaling molecules-are critically involved in osteoblast differentiation and skeletal homeostasis. We examined whether the capacity of rat osteoblastic cells to form gap junctions and respond to known modulators of gap junction intercellular communication (GJIC) was dependent on the age of the animal from which they were isolated. We observed no effect of age upon osteoblastic Cx43 mRNA, protein or GJIC. We also examined age-related changes in PTH-stimulated GJIC. PTH demonstrated age-dependent effects upon GJIC: Osteoblastic cells from young rats increased GJIC in response to PTH, whereas there was no change in GJIC in response to PTH in osteoblastic cells from mature or old rats. PTH-stimulated GJIC occurred independently of changes in Cx43 mRNA or protein expression. Cholera toxin significantly increased GJIC in osteoblastic cells from young rats compared to those from mature and old rats. These data demonstrate an age-related impairment in the capacity of osteoblastic cells to generate functional gap junctions in response to PTH, and suggest that an age-related defect in G protein-coupled adenylate cyclase activity at least partially contributes to decreased PTH-stimulated GJIC.

AB - Aging demonstrates deleterious effects upon the skeleton which can predispose an individual to osteoporosis and related fractures. Despite the well-documented evidence that aging decreases bone formation, there remains little understanding whereby cellular aging alters skeletal homeostasis. We, and others, have previously demonstrated that gap junctions-membrane-spanning channels that allow direct cell-to-cell conductance of small signaling molecules-are critically involved in osteoblast differentiation and skeletal homeostasis. We examined whether the capacity of rat osteoblastic cells to form gap junctions and respond to known modulators of gap junction intercellular communication (GJIC) was dependent on the age of the animal from which they were isolated. We observed no effect of age upon osteoblastic Cx43 mRNA, protein or GJIC. We also examined age-related changes in PTH-stimulated GJIC. PTH demonstrated age-dependent effects upon GJIC: Osteoblastic cells from young rats increased GJIC in response to PTH, whereas there was no change in GJIC in response to PTH in osteoblastic cells from mature or old rats. PTH-stimulated GJIC occurred independently of changes in Cx43 mRNA or protein expression. Cholera toxin significantly increased GJIC in osteoblastic cells from young rats compared to those from mature and old rats. These data demonstrate an age-related impairment in the capacity of osteoblastic cells to generate functional gap junctions in response to PTH, and suggest that an age-related defect in G protein-coupled adenylate cyclase activity at least partially contributes to decreased PTH-stimulated GJIC.

KW - aging

KW - connexion 43

KW - gap junction

KW - osteoblast

KW - parathyroid hormone

UR - http://www.scopus.com/inward/record.url?scp=84867841673&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84867841673&partnerID=8YFLogxK

U2 - 10.1002/jor.22172

DO - 10.1002/jor.22172

M3 - Article

C2 - 22696456

AN - SCOPUS:84867841673

VL - 30

SP - 1979

EP - 1984

JO - Journal of Orthopaedic Research

JF - Journal of Orthopaedic Research

SN - 0736-0266

IS - 12

ER -