News Release 

Researchers uncover novel amyloidosis

Tokyo University of Agriculture and Technology


IMAGE: A collaboration led by scientists at Tokyo University of Agriculture and Technology (TUAT), Japan, has discovered a novel amyloid protein that induces amyloidosis in rats. This new amyloid protein... view more 

Credit: Tomoaki Murakami, TUAT

A collaboration led by scientists at Tokyo University of Agriculture and Technology (TUAT), Japan, has discovered a novel amyloid protein that induces amyloidosis in rats. This new amyloid protein is known to be the lipopolysaccharide binding protein (LBP) and accumulated very frequently in the mammary gland of aged rats. Although LBP was identified as an amyloid protein by this research using rats, learning from rats is very important for understanding the cause of human diseases because a human also has LBP. Hence, their findings of this research are useful for predicting the future occurrence of human amyloidosis and as a disease model animal.

The researchers published their results on Oct 15th in Amyloid.

Amyloidosis is a disease group showing the deposition of amyloid that is misfolded protein originating from the host protein, i.e., this case LBP. For amyloidosis, unfortunately, no cure is available, but treatments can help symptoms and produce less amyloid protein.

"When looking into mammary glands of old rats, interestingly we very often saw needle-shaped amyloid", said Tomoaki Murakami, DVM, PhD, the first and corresponding author on the paper and Associate Professor in Laboratory of Veterinary Toxicology, Cooperative Department of Veterinary Medicine at TUAT. Amyloid deposition was actually observed in 83% of aged female rats. "We are very surprised at this finding, because it was known that in rats amyloidosis is extremely rare and that spontaneous rat amyloidosis had not been reported for about half a century."

In contrast to old rats, in younger rats, amyloid deposition was not at all observed. The difference between the aged and youth was the presence or absence of an intra-mammary gland structure called "Corpora amylacea", which are round, glass-like substances, meaning "starch-like bodies" in Latin. "We found that the needle-shaped amyloid was always formed on the surface of Corpora amylacea", said Murakami.

"After we carried out histological, immunohistochemical, ultrastructural, and proteomic analysis, LBP was identified as a prime candidate for amyloid protein," according to Murakami. LBP is known to be involved in innate immunity and is expressed in various animal species including humans.

"We would like to point out that we discovered novel amyloidosis in rats and that Corpora amylacea formation during aging is its risk factors. In human, iatrogenic amyloidosis and transmissible amyloidosis have been reported as non-spontaneous amyloidosis. We expect that this study provides useful information for predicting the accidentally induced amyloidosis in human that may occur in the future", Murakami added.


For information about the Murakami laboratory, please visit

This research was partially supported by JSPS KAKENHI (Grant Numbers 16H05027 and 17K17702) and TUAT President's Discretionary Funding to support the launch of next-generation research project.

About Tokyo University of Agriculture and Technology (TUAT):

TUAT is a distinguished university in Japan dedicated to science and technology. TUAT focuses on agriculture and engineering that form the foundation of industry, and promotes education and research fields that incorporate them. Boasting a history of over 140 years since our founding in 1874, TUAT continues to boldly take on new challenges and steadily promote fields. With high ethics, TUAT fulfills social responsibility in the capacity of transmitting science and technology information towards the construction of a sustainable society where both human beings and nature can thrive in a symbiotic relationship. For more information, please visit

Original Publication:

Needle-shaped amyloid deposition in rat mammary gland: evidence of a novel amyloid fibril protein. Tomoaki Murakami*, Keiichi Noguchi, Naomi Hachiya, Fuyuki Kametani, Masayoshi Tasaki, Satoshi Nakaba, Yukiko Sassa, Taro Yamashita, Konen Obayashi, Yukio Ando, Masao Hamamura, Takeshi Kanno, and Kazufumi Kawasako.

Amyloid, 2019, Oct 15:1-11


Tomoaki Murakami, DVM, PhD.
Associate Professor,
Laboratory of Veterinary Toxicology, Cooperative Department of Veterinary Medicine, TUAT, Japan

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