|
|
|
Dena
Howland |
 |
| Dena
Howland studies behavioral and anatomical recovery in the injured
central nervous system with emphasis on regeneration, neural tissue
transplantation, spinal cord injury and repair and locomotor function. |
 |
Associate Professor of Neuroscience
Investigator, McKnight Brain Institute
Training
Postdoc - University of Florida, Department of Neuroscience
and Gainesville VA Medical Center, Mentor: Douglas K. Anderson
Ph.D. Medical College of Pennsylvania, Philadelphia, PA
B.S. Ohio State University, Columbus, Ohio
|
Contact
phone:
352.294.0028
office: MBI L1-100G
lab: MBI L2-160
email:howland@mbi.ufl.edu
|
|
| The
overall focus of the laboratory is to determine how the spinal
cord responds to injury and what interventions may be used to
enhance recovery based upon both anatomical and behavioral criteria.
A variety of lesion models in both the rat and cat are being
used. Our studies have shown that grafts of embryonic spinal
cord can promote recovery following spinal cord injury in both
developing and adult systems. A variety of neuroanatomical and
molecular methods are being used to assess the cellular and
axonal interactions that occur between the host and graft. We
are also currently studying the expression of several molecules
that are know to affect axonal growth during development. The
behavioral analyses focuses on several characteristics of locomotion
including weight support, balance, interlimb coordination and
angular kinematics. |
Recent
Publications
Intact
aggrecan and chondroitin sulfate-depleted aggrecan core glycoprotein
inhibit axon growth in the adult rat spinal cord. Lemons
ML, Sandy JD, Anderson DK, Howland DR. Exp Neurol. 2003 Dec;184(2):981-90.
Intact aggrecan and fragments generated by both aggrecanse and
metalloproteinase-like activities are present in the developing
and adult rat spinal cord and their relative abundance is altered
by injury. Lemons ML, Sandy JD, Anderson DK, Howland DR.
J Neurosci. 2001 Jul 1;21(13):4772-81.
Chondroitin sulfate proteoglycan immunoreactivity increases
following spinal cord injury and transplantation. Lemons
ML, Howland DR, Anderson DK. Exp Neurol. 1999 Nov;160(1):51-65.
|
|
|