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Calbindin-D(28K) cells selectively contact intra-SCN neurons
J LeSauter1, L J Kriegsfeld, J Hon
1Department of Psychology, Barnard College, New York, NY 10027, USA.
Neuroscience
|May 29, 2002
Summary
Calbindin-D(28K) cells in the hamster suprachiasmatic nucleus receive input from various peptides. These cells show specialized topographical organization and reciprocal connections, crucial for understanding circadian rhythm regulation.
Area of Science:
- Neuroscience
- Chronobiology
- Cell Biology
Background:
- Calbindin-D(28K)-immunoreactive cells are located in the suprachiasmatic nucleus (SCN) of hamsters.
- These cells receive direct retinal input and are activated by light pulses, indicated by Fos expression.
- Understanding the afferent and efferent connections of these cells is vital for comprehending SCN organization.
Purpose of the Study:
- To investigate the interconnections between calbindin-D(28K) cells and other peptidergic cells within the SCN.
- To map the afferent and efferent connections of calbindin-D(28K) cells in the hamster SCN.
Main Methods:
- Epi- and confocal microscopy were employed to visualize cellular interactions.
- Intra-suprachiasmatic nucleus tract tracing techniques were utilized to identify neuronal projections.
- Biotinylated dextran amine injections into the SCN were used to trace efferent pathways.
Main Results:
- Calbindin-D(28K) cells receive significant input from vasoactive intestinal polypeptide (VIP), neuropeptide Y, and serotonin fibers.
- Most calbindin-D(28K) cells also receive input from gastrin-releasing peptide (GRP) and cholecystokinin (CCK) fibers.
- Reciprocal connections were observed with VIP, GRP, and CCK cells, but not with dorsomedial vasopressin cells.
Conclusions:
- The study reveals a highly specialized topographical organization of connections within the SCN.
- A significant percentage of substance P, GRP, and VIP cells within the calbindin subnucleus coexpress calbindin-D(28K).
- These findings enhance our understanding of neuronal circuitry and information processing in the SCN, the master circadian clock.