2007
DOI: 10.1016/j.jneuroim.2007.02.010
|View full text |Cite
|
Sign up to set email alerts
|

β2-Adrenergic receptor-dependent sexual dimorphism for murine leukocyte migration

Abstract: In wild-type FVB mice, leukocyte recruitment to lipopolysaccharide was sexually dimorphic, with a greater number of leukocytes recruited in females. In male β 2 -adrenergic receptor knock out mice (bred on a congenic FVB background) the number leukocytes recruited was increased ~4-fold, while in females there was no change, eliminating sexual dimorphism in leukocyte migration. While there were significantly fewer recruited CD62L + and CD11a + leukocytes in wild-type males, only in male β 2 -adrenergic receptor… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

1
8
0

Year Published

2009
2009
2024
2024

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 10 publications
(9 citation statements)
references
References 97 publications
1
8
0
Order By: Relevance
“…However, a decrease of 1.5 times of the stiffness under Ca 2+ load promotes the intensive use of the membrane reserve by cells during the regulation of their volume in a hypotonic medium. The effects discussed are closely connected with the mechanism of regulation of cell surface stiffness through the elements of cytoskeleton (de Coupade et al 2007;Feske 2007;Insall and Machesky 2009) and generally agree with the results obtained in the present work.…”
Section: Discussionsupporting
confidence: 90%
“…However, a decrease of 1.5 times of the stiffness under Ca 2+ load promotes the intensive use of the membrane reserve by cells during the regulation of their volume in a hypotonic medium. The effects discussed are closely connected with the mechanism of regulation of cell surface stiffness through the elements of cytoskeleton (de Coupade et al 2007;Feske 2007;Insall and Machesky 2009) and generally agree with the results obtained in the present work.…”
Section: Discussionsupporting
confidence: 90%
“…1). Next, to determine if NLB induces plasticity in nociceptor function we evaluated the hyperalgesia induced by a well-studied inflammatory mediator, PGE 2 , which produces a markedly prolonged hyperalgesia after adult exposure to stress [30], hyperalgesia that is mediated by a second messenger (PKCε) dependent signaling pathway [17,20,21,44]. In both naive control and NLB rats, PGE 2 (1 μg, into the gastrocnemius muscle)induced mechanical hyperalgesia with a rapid onset.…”
Section: Resultsmentioning
confidence: 99%
“…NLB-treatment produced mechanical hyperalgesia in skeletal muscle and prolongation of inflammatory mediator-induced hyperalgesia (i.e., hyperalgesic priming) [17], as well as hyperalgesic priming in the cutaneous domain, measured in adult rats. While treatment with PKCε antisense in adult NLB-treated rats only slightly reduced ongoing mechanical hyperalgesia in muscle, but not skin, it completely reversed hyperalgesic priming in both muscle and skin, implicating a role of PKCε in this effect of early-life stress.…”
Section: Discussionmentioning
confidence: 99%
“…Such sexual dimorphism is common: in the liver, for example, a large number of genes are sex-specific, with STAT5a playing a key role in regulating sex-specific gene expression in the female liver and STAT5b in the male liver29. The beta(2)-adrenergic receptor on male leukocytes appears to contribute to sexual dimorphism in murine leukocyte migration30. In the ear, mice lacking the GABA(A) receptor subunit beta2 display a clear sexual dimorphism in cochlear phenotype31.…”
Section: Discussionmentioning
confidence: 99%