Search Results

You are looking at 1 - 10 of 11 items for :

  • endothelium x
  • Refine by access: Open Access content only x
Clear All
Xiang Xiao Center for Biomedical Research, Population Council, 1230 York Avenue, New York, New York 10065, USA

Search for other papers by Xiang Xiao in
Google Scholar
PubMed
Close
,
C Yan Cheng Center for Biomedical Research, Population Council, 1230 York Avenue, New York, New York 10065, USA

Search for other papers by C Yan Cheng in
Google Scholar
PubMed
Close
, and
Dolores D Mruk Center for Biomedical Research, Population Council, 1230 York Avenue, New York, New York 10065, USA

Search for other papers by Dolores D Mruk in
Google Scholar
PubMed
Close

In this study, we investigated the role of intercellular adhesion molecule-2 (ICAM2) in the testis. ICAM2 is a cell adhesion protein having important roles in cell migration, especially during inflammation when leukocytes cross the endothelium. Herein, we showed ICAM2 to be expressed by germ and Sertoli cells in the rat testis. When a monospecific antibody was used for immunolocalization experiments, ICAM2 was found to surround the heads of elongating/elongated spermatids in all stages of the seminiferous epithelial cycle. To determine whether ICAM2 is a constituent of apical ectoplasmic specialization (ES), co-immunoprecipitation and dual immunofluorescence staining were performed. Interestingly, ICAM2 was found to associate with β1-integrin, nectin-3, afadin, Src, proline-rich tyrosine kinase 2, annexin II, and actin. Following CdCl2 treatment, ICAM2 was found to be upregulated during restructuring of the seminiferous epithelium, with round spermatids becoming increasingly immunoreactive for ICAM2 by 6–16 h. Interestingly, there was a loss in the binding of ICAM2 to actin during CdCl2-induced germ cell loss, suggesting that a loss of ICAM2–actin interactions might have facilitated junction restructuring. Taken collectively, these results illustrate that ICAM2 plays an important role in apical ES dynamics during spermatogenesis.

Open access
Laura L Hernandez Department of Animal Sciences, Department of Molecular and Cellular Physiology, University of Arizona, Tucson, Arizona 85721, USA
Department of Animal Sciences, Department of Molecular and Cellular Physiology, University of Arizona, Tucson, Arizona 85721, USA

Search for other papers by Laura L Hernandez in
Google Scholar
PubMed
Close
,
Sean W Limesand Department of Animal Sciences, Department of Molecular and Cellular Physiology, University of Arizona, Tucson, Arizona 85721, USA

Search for other papers by Sean W Limesand in
Google Scholar
PubMed
Close
,
Jayne L Collier Department of Animal Sciences, Department of Molecular and Cellular Physiology, University of Arizona, Tucson, Arizona 85721, USA

Search for other papers by Jayne L Collier in
Google Scholar
PubMed
Close
,
Nelson D Horseman Department of Animal Sciences, Department of Molecular and Cellular Physiology, University of Arizona, Tucson, Arizona 85721, USA

Search for other papers by Nelson D Horseman in
Google Scholar
PubMed
Close
, and
Robert J Collier Department of Animal Sciences, Department of Molecular and Cellular Physiology, University of Arizona, Tucson, Arizona 85721, USA

Search for other papers by Robert J Collier in
Google Scholar
PubMed
Close

myoepithelial cells, and asteriks (*) correspond to vascular endothelium. Expression of HTR1B , 2A , 2B , 4 , and 7 was each localized in BMT ( Fig. 2 , row A, columns 1–5). Counterstaining with GS-I (vascular endothelium) indicated that HTR1B , 2A , and

Open access
Colin P Sibley Maternal and Fetal Health Research Centre, Division of Developmental Biology and Medicine, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK
St Mary’s Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK

Search for other papers by Colin P Sibley in
Google Scholar
PubMed
Close

cytotrophoblast (EVT) cells invade the spiral arteries so that both the endothelium and smooth muscle of the vessels are eroded ( Burton et al . 2017 ). This invasion by the EVT is extensive and initially plugs the terminal end of the vessels, preventing any

Open access
Graham W Aberdeen Departments of Obstetrics, Gynecology, Reproductive Sciences and Physiology, University of Maryland School of Medicine, Baltimore, Maryland, USA

Search for other papers by Graham W Aberdeen in
Google Scholar
PubMed
Close
,
Jeffery S Babischkin Departments of Obstetrics, Gynecology, Reproductive Sciences and Physiology, University of Maryland School of Medicine, Baltimore, Maryland, USA

Search for other papers by Jeffery S Babischkin in
Google Scholar
PubMed
Close
,
Gerald J Pepe Department of Physiological Sciences, Eastern Virginia Medical School, Norfolk, Virginia, USA

Search for other papers by Gerald J Pepe in
Google Scholar
PubMed
Close
, and
Eugene D Albrecht Departments of Obstetrics, Gynecology, Reproductive Sciences and Physiology, University of Maryland School of Medicine, Baltimore, Maryland, USA

Search for other papers by Eugene D Albrecht in
Google Scholar
PubMed
Close

Mediation by M 3 -muscarinic receptors of both endothelium-dependent contraction and relaxation to acetylcholine in the aorta of the spontaneously hypertensive rat . British Journal of Pharmacology 112 519 – 524 . ( https://doi.org/10.1111/j.1476

Open access
Antonia Hufnagel University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Level 4, Addenbrooke’s Hospital, Cambridge, Cambridgeshire, UK

Search for other papers by Antonia Hufnagel in
Google Scholar
PubMed
Close
,
Laura Dearden University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Level 4, Addenbrooke’s Hospital, Cambridge, Cambridgeshire, UK

Search for other papers by Laura Dearden in
Google Scholar
PubMed
Close
,
Denise S Fernandez-Twinn University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Level 4, Addenbrooke’s Hospital, Cambridge, Cambridgeshire, UK

Search for other papers by Denise S Fernandez-Twinn in
Google Scholar
PubMed
Close
, and
Susan E Ozanne University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Level 4, Addenbrooke’s Hospital, Cambridge, Cambridgeshire, UK

Search for other papers by Susan E Ozanne in
Google Scholar
PubMed
Close

. 2018 ). In 1994 Desoye et al . reported that insulin receptor protein expression shifts from the maternal facing side of the placenta (the syncytiotrophoblast) to the fetal facing side of the placenta (the fetal endothelium) with advancing gestation in

Open access
Jeffrey Friedman Rockefeller University, Box 305, 1230 York Avenue, New York, New York 10065, USA

Search for other papers by Jeffrey Friedman in
Google Scholar
PubMed
Close

questions remain unanswered including the aforementioned. How is leptin transported into the CNS? Previous studies suggested that leptin entered the brain by transport across the vascular endothelium ( Banks & Farrell 1999 , Banks & Farrell 2003 ). However

Open access
Katie J Mylonas University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Katie J Mylonas in
Google Scholar
PubMed
Close
,
Neil A Turner Division of Cardiovascular & Diabetes Research, Leeds Institute of Cardiovascular & Metabolic Medicine (LICAMM), School of Medicine, University of Leeds, Leeds, UK

Search for other papers by Neil A Turner in
Google Scholar
PubMed
Close
,
Sumia A Bageghni Division of Cardiovascular & Diabetes Research, Leeds Institute of Cardiovascular & Metabolic Medicine (LICAMM), School of Medicine, University of Leeds, Leeds, UK

Search for other papers by Sumia A Bageghni in
Google Scholar
PubMed
Close
,
Christopher J Kenyon University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Christopher J Kenyon in
Google Scholar
PubMed
Close
,
Christopher I White University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Christopher I White in
Google Scholar
PubMed
Close
,
Kieran McGregor University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Kieran McGregor in
Google Scholar
PubMed
Close
,
Robert A Kimmitt University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Robert A Kimmitt in
Google Scholar
PubMed
Close
,
Richard Sulston University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Richard Sulston in
Google Scholar
PubMed
Close
,
Valerie Kelly University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Valerie Kelly in
Google Scholar
PubMed
Close
,
Brian R Walker University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Brian R Walker in
Google Scholar
PubMed
Close
,
Karen E Porter Division of Cardiovascular & Diabetes Research, Leeds Institute of Cardiovascular & Metabolic Medicine (LICAMM), School of Medicine, University of Leeds, Leeds, UK

Search for other papers by Karen E Porter in
Google Scholar
PubMed
Close
,
Karen E Chapman University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Karen E Chapman in
Google Scholar
PubMed
Close
, and
Gillian A Gray University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK

Search for other papers by Gillian A Gray in
Google Scholar
PubMed
Close

LS Nash GB McGettrick HM 2016 Comparative ability of mesenchymal stromal cells from different tissues to limit neutrophil recruitment to inflamed endothelium . PLoS ONE 11 e0155161 . ( doi:10.1371/journal.pone.0155161 ) Nagase H

Open access
David O'Regan Endocrinology Unit, Queen's Medical Research Institute, Centre for Cardiovascular Science, 47 Little France Crescent, Edinburgh EH16 4TJ, UK

Search for other papers by David O'Regan in
Google Scholar
PubMed
Close
,
Christopher J Kenyon Endocrinology Unit, Queen's Medical Research Institute, Centre for Cardiovascular Science, 47 Little France Crescent, Edinburgh EH16 4TJ, UK

Search for other papers by Christopher J Kenyon in
Google Scholar
PubMed
Close
,
Jonathan R Seckl Endocrinology Unit, Queen's Medical Research Institute, Centre for Cardiovascular Science, 47 Little France Crescent, Edinburgh EH16 4TJ, UK

Search for other papers by Jonathan R Seckl in
Google Scholar
PubMed
Close
, and
Megan C Holmes Endocrinology Unit, Queen's Medical Research Institute, Centre for Cardiovascular Science, 47 Little France Crescent, Edinburgh EH16 4TJ, UK

Search for other papers by Megan C Holmes in
Google Scholar
PubMed
Close

: MacGraw Hill . Fulton CT Stallone JN 2002 Sexual dimorphism in prostanoid-potentiated vascular contraction: roles of endothelium and ovarian steroids . American Journal of Physiology 283 H2062 – H2073 . Garcia

Open access
T’ng Choong Kwok University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, United Kingdom

Search for other papers by T’ng Choong Kwok in
Google Scholar
PubMed
Close
and
Roland H Stimson University/BHF Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, United Kingdom

Search for other papers by Roland H Stimson in
Google Scholar
PubMed
Close

technique uses fluorescent imaging probes that accumulate in BAT ( Azhdarinia et al. 2013 , Zhang et al. 2015 ). For example, PEP3 is a peptide that binds to receptors on the endothelium of BAT and beige adipose tissue, which when conjugated with a

Open access
Bin Li School of Basic Medical Sciences, Capital Medical University, Beijing, China

Search for other papers by Bin Li in
Google Scholar
PubMed
Close
,
Jiming Yin Beijing You An Hospital, Capital Medical University, Beijing, China
Beijing Institute of Hepatology, Beijing, China

Search for other papers by Jiming Yin in
Google Scholar
PubMed
Close
,
Jing Chang Beijing You An Hospital, Capital Medical University, Beijing, China

Search for other papers by Jing Chang in
Google Scholar
PubMed
Close
,
Jia Zhang School of Basic Medical Sciences, Capital Medical University, Beijing, China

Search for other papers by Jia Zhang in
Google Scholar
PubMed
Close
,
Yangjia Wang School of Basic Medical Sciences, Capital Medical University, Beijing, China

Search for other papers by Yangjia Wang in
Google Scholar
PubMed
Close
,
Haixia Huang School of Basic Medical Sciences, Capital Medical University, Beijing, China

Search for other papers by Haixia Huang in
Google Scholar
PubMed
Close
,
Wei Wang School of Basic Medical Sciences, Capital Medical University, Beijing, China
Beijing Lab for Cardiovascular Precision Medicine, Beijing, China

Search for other papers by Wei Wang in
Google Scholar
PubMed
Close
, and
Xiangjun Zeng School of Basic Medical Sciences, Capital Medical University, Beijing, China

Search for other papers by Xiangjun Zeng in
Google Scholar
PubMed
Close

cell-specific proteins, was detected. The results showed that the number of E-cadherin+ cells in the endothelium of arterioles of heart were significantly decreased in kkAy mice compared to C57 mice (diabetic effects, P  <0.01), which were

Open access