Identification of Neurite Outgrowth Promoting Sites on the Laminin α3 Chain G Domain

• Published in: Biochemistry (Easton) Vol. 41; no. 35; pp. 10747 - 10753
• Main Authors: Kato, Kozue, Utani, Atsushi, Suzuki, Nobuharu, Mochizuki, Mayumi, Yamada, Masanori, Nishi, Norio, Matsuura, Hiroshi, Shinkai, Hiroshi, Nomizu, Motoyoshi
• Format: Journal Article
• Language: English
• Published: American Chemical Society 03.09.2002
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi020180k

Laminins are expressed in specific tissues and are involved in various biological activities including promoting cell adhesion, growth, migration, neurite outgrowth, and differentiation. The laminin α3 chain is mainly located in the skin and is also expressed in the floor plate of the developing neural tube. Previously, we showed that the human laminin α3 chain LG4 module binds to syndecan-2/4, a membrane-associated proteoglycan, and promotes human fibroblast adhesion. Here, we have evaluated the neurite outgrowth activity of the laminin α3 chain LG4 and LG5 modules. Three overlapping recombinant proteins, which contained LG4 and/or LG5 modules of the human laminin α3 chain, were prepared using a mammalian cell expression system. Two proteins, rec-α3LG4-5 and rec-α3LG4, promoted cell attachment and neurite outgrowth of rat pheochromocytoma PC12 cells, but rec-α3LG5 was inactive. Twenty-two peptides covering the entire LG4 module were synthesized and tested for cell attachment and neurite outgrowth activity to identify active sites of the LG4 module. A3G75 (KNSFMALYLSKG, α3 chain 1411−1422) and A3G83 (GNSTISIRAPVY, α3 chain 1476−1487) promoted PC12 cell attachment and neurite outgrowth. Additionally, A3G75 and A3G83 inhibited PC12 cell attachment to rec-α3LG4. These results suggest that the A3G75 and A3G83 sites are important for PC12 cell attachment and neurite outgrowth in the laminin α3 chain LG4 module. We also conjugated the A3G75 and A3G83 peptides on chitosan membranes to test their potential as bio-materials. These peptide-conjugated chitosan membranes were more active for neurite outgrowth than the peptide-coated plates. These results suggest that the A3G75- and A3G83-conjugated chitosan membranes are applicable as bio-medical materials for neural tissue repair and engineering.