Gerald Kidder

Genetics & Development Dr. Gerald Kidder
Chair
Photo

Affiliations

Chair, Division of Genetics & Development, Children’s Health Research Institute
Distinguished University Professor Emeritus, Western University
Adjunct Professor, Department of Physiology & Pharmacology, Schulich School of Medicine & Dentistry, Western University

How my research helps children

My research helps children in two ways.  First, my team studies mice that have gene mutations that are the same as those that cause certain birth defects in human babies.  By studying the effects of these mutations in mice, we can get a better understanding of how the mutations disrupt normal development and what can be done to minimize their effects.  Second, our research in the development of egg cells, also using mice, has provided new insight into the factors that control egg cell development and the importance of those factors for the health of embryos.  The results of this research are being applied to ensuring the health of babies conceived through in vitro fertilization.

Research

Current Research Activities

  1. Structural determinants of connexin specificity: this NSERC-funded research program relies on genetically modified mice to explore the structural components of connexins, gap junction-forming proteins, necessary for their functions in spermatogenesis.  The aim is to improve our understanding of how the structure of a particular connexin determines its unique functions in the development of sperm cells.
  2. Roles of gap junctional coupling in oogenesis: funded by CIHR, this research also uses genetically modified mice.  It is aimed at elucidating the roles that connexins play in the growth of ovarian follicles and the production of developmentally competent oocytes.  We are also studying the paracrine signaling pathways that may interact with gap junctional communication in these processes.  Insights from this mouse work are being used to improve the understanding and treatment of human female infertility.
  3. Non-invasive assessment of oocyte quality in assisted conception: this project was initially funded by CIHR and later by the Western Innovation Fund, an internal UWO fund for the commercialization of intellectual property.  We have used information obtained from our studies of mutant mice to devise a test of human oocyte quality to improve the outcome of in vitro fertilization.  The research utilizes follicle (cumulus) cells, obtained during oocyte retrieval, which would otherwise be discarded.
  4. Cx43 mutations linked to human disease: this CIHR-funded project in collaboration with UWO colleagues Donglin Bai and Dale Laird is aimed at understanding how mutations in the gene encoding connexin43 cause the diverse features of the congenital malformation, oculodentodigital dysplasia (ODDD).  The experiments utilize both cell cultures (tissue biopsies from ODDD patients) and mice carrying ODDD-causing mutations.
  5. Training Program in Reproduction, Early Development, and the Impact on Health (REDIH): this Strategic Training Program in Health Research, funded by CIHR, employs the collective expertise of 30 researchers in reproductive biology and reproductive medicine from Western, McMaster, McGill, Laval, the University of Ottawa, and the University of Montreal.  It provides stipend support for clinical residents, graduate students, and postdoctoral research fellows to conduct basic research in developmental biology related to reproductive medicine.

Research Team

The current team consists of two technicians, two postdoctoral fellows, and two undergrads.  Past trainees have gone on to become doctors, dentists, college or university professors, university administrators, research institute directors, biotech company executives, research technicians, business professionals, high school teachers, and a variety of other types of professionals.

Future Research Plans

Our ultimate goal is to work with clinics and private companies to translate our discoveries into practical applications that will ensure the health of children.

Awards & Grants

Awards & Grants

Fellowship in support of Paul Dyce for "The WNT signalling pathway and its involvement in follicular and oocyte competence" – Awarded by Canadian Institute of Health Research (CIHR)

Distinguished University Professorship Award – Awarded by Western University (2010)

Turner Society Award for Excellence Distinction – Awarded by Hiram College, USA (2006)

Funding support for “Training program in reproduction, early development, and the impact on health” – Awarded by Canadian Institute of Health Research (CIHR)

Funding support for “Cx43 mutations linked to human disease” – Awarded by CIHR

Funding support for “Roles of gap junctional coupling in oogenesis” – Awarded by CIHR

Funding support for “Structural determinants of connexin specificity” – Awarded by Natural Sciences and Engineering Research Council of Canada (NSERC)

Recent Publications

Publications

Training program in reproduction, early development, and the impact on health (REDIH): Evaluation of year 1
MacDonald CJ, Archibald D, Batlz JM, Kidder GM, Clarke H. J Studies Education 2:1-28. 2012

Male reproductive system defects and subfertility in a mutant mouse model of oculodentodigital dysplasia
Gregory M, Kahiri CN, Barr JK, Smith CE, Hermo L, Cyr DG, Kidder GM. Int J Androl. 34: e630-e641. 2011

In vitro and in vivo germ line potential of stem cells derived from newborn mouse skin
Dyce PW, Liu J, Tayade C, Kidder GM, Betts DH, Li J. PLoS ONE 6:e20339. 2011

WNT2 regulates DNA synthesis in mouse granulosa cells through beta-catenin
Wang HX, Li TY, Kidder GM.Biol Reprod. 2010 May;82(5):865-75

Reduction of electrical coupling between microvascular endothelial cells by NO depends on connexin37 McKinnon RL, Bolon ML, Wang HX, Swarbreck S, Kidder GM, Simon AM,
Tyml K. Am J Physiol Heart Circ Physiol. 2009 Jul;297(1):H93-H101

Oogenesis defects in a mutant mouse model of oculodentodigital dysplasia
Tong D, Colley D, Thoo R, Li TY, Plante I, Laird DW, Bai D, Kidder GM.
Dis Model Mech. 2009 Mar-Apr;2(3-4):157-67

A dominant loss-of-function GJA1 (Cx43) mutant impairs parturition in the mouse.
Tong D, Lu X, Wang HX, Plante I, Lui E, Laird DW, Bai D, Kidder GM.
Biol Reprod. 2009 Jun;80(6):1099-106.

Identification of WNT/beta-CATENIN signaling pathway components in human cumulus cells
Wang HX, Tekpetey FR, Kidder GM Mol Hum Reprod. 2009 Jan;15(1):11-7.

Lipopolysaccharide plus hypoxia and reoxygenation synergistically reduce electrical coupling between microvascular endothelial cells by dephosphorylating connexin40.
Bolon ML, Peng T, Kidder GM, Tyml K. J Cell Physiol. 2008 Nov;217(2):350-9.

ODDD-linked Cx43 mutants reduce endogenous Cx43 expression and function in osteoblasts and inhibit late stage differentiation.
McLachlan E, Plante I, Shao Q, Tong D, Kidder GM, Bernier SM, Laird DW
J Bone Miner Res. 2008 Jun;23(6):928-38.

Rescue of oogenesis in Cx37-null mutant mice by oocyte-specific replacement with Cx43
Li TY, Colley D, Barr KJ, Yee SP, Kidder GM. J Cell Sci. 2007 Dec 1;120(Pt 23):4117-25.

In vivo analysis of undocked connexin43 gap junction hemichannels in ovarian granulosa cells.
Tong D, Li TY, Naus KE, Bai D, Kidder GM J Cell Sci. 2007 Nov 15;120(Pt 22):4016-24.

Connexin levels regulate keratinocyte differentiation in the epidermis
Langlois S, Maher AC, Manias JL, Shao Q, Kidder GM, Laird DW
J Biol Chem. 2007 Oct 12;282(41):30171-80

Additional publications

Contact

Phone: 519-661-3132
Fax: 519-850-2562
Email: gerald [dot] kidder [at] schulich [dot] uwo [dot] ca
Website: http://www.chri.org/db/kidder.htm

(Please note: CHRI is not responsible for the content of any external sites - links will open in new window)